Syngene International Limited | Hyderabad (Kolthur, Shamirpet, Medchal, Telangana)

Research Associate

Role & responsibilities

• You will clearly synthesize, package, articulate and deliver your findings in a timely and accurate manner and conduct research on commercial, multi-industry and economic topics.

• Excellent organizational skills are essential for successfully managing a variety and volume of research requests by accurately summarizing data and facts into appropriate and timely output i.e. email, Excel, PowerPoint, Word. Along with supporting research products (i.e. news alerts, company profiles etc.), you will also contribute to knowledge capture and documentation.

• Company's Health Care practice serve clients across the health care value chain, including the worlds leading pharmaceutical and biotech companies, medical technology companies, health care payers and providers, health care systems and services, as well as trusts and foundations serving a global health mission.

Your qualifications

• Undergraduate degree minimum (Pharmacy, Biotechnology, or Biomedical sciences) with high academic record

• 0-1 years of relevant working experience, in Pharma, healthcare, medical devices and Biotech domain. Basic understanding of the health care space with prime focus on pharma

• Excellent English; verbal and written

• Ability to work with wide array of platforms including Excel, Word, and PowerPoint; to be able to provide insights in most user-friendly format. Knowledge of AI tools like ChatGPT

Freshers should have internship experience in secondary research domain. 3- 6 months experience candidates can also apply.

Please share your resumes on alpa.jain@persolapac.com/bhakti.tanna@persolapac.com

Pharmacovigilance Intern

About the job

For the past 20 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies. ProPharma partners with its clients through an advise-build-operate model across the complete product lifecycle. With deep domain expertise in regulatory sciences, clinical research solutions, quality & compliance, pharmacovigilance, medical information, and R&D technology, ProPharma offers an end-to-end suite of fully customizable consulting solutions that de-risk and accelerate our partners’ most high-profile drug and device programs.

Job Title: Pharmacovigilance Intern
Location: Hyderabad (Work from Office)
Duration: 12 Months
Department: Pharmacovigilance

About The Role

We are offering an exciting internship opportunity in the Pharmacovigilance department for individuals with experience in the Argus safety database. This role will provide hands-on experience in drug safety processes, case management, and regulatory reporting, helping interns build a strong foundation in pharmacovigilance.

Key Responsibilities

• • Manage assigned mailboxes, including inbox triage of client communication, inbound reports, and internal case processing communications.

  • Perform Duplicate searches and complete initial book-in as required.

  • Enter basic data into safety database as required such as identifiable patient, report, suspect drug, and adverse event.

  • Assist in case processing within the Argus database, including follow-ups.

  • Assist in Narrative Writing, MedDRA Coding.

  • Support in Individual Case Safety Report (ICSR) management, ensuring compliance with regulatory requirements.

  • Work with cross-functional teams to ensure timely adverse event reporting.

  • Maintain accurate documentation and adhere to pharmacovigilance compliance standards.

Requirements

• • Completed a degree in Pharmacy, Life Sciences, Medicine, or a related field.

  • Basic knowledge and prior training/experience with Argus safety database is required.

  • Understanding of pharmacovigilance principles and drug safety regulations.

  • Strong attention to detail, analytical skills, and ability to work in a fast-paced environment.

  • Proficiency in Microsoft Office (Word, Excel, PowerPoint).

  • Strong verbal, written and interpersonal communication skills. 

What We Offer

• Hands-on experience in a global pharmacovigilance setting.

• Exposure to real-world case processing and regulatory requirements.

• Mentorship and training from industry experts.

• Opportunity to enhance career prospects in drug safety and regulatory affairs.

We celebrate our differences and strive to create a workplace where each person can be their authentic self. We are committed to diversity, equity, and inclusion. Employees are encouraged to unleash their innovative, collaborative, and entrepreneurial spirits. With a holistic approach as an Equal Opportunity Employer, we provide a safe space where all employees feel empowered to succeed.

ProPharma Group does not accept unsolicited resumes from recruiters/third parties. Please, no phone calls or emails to anyone regarding this posting.

Market Research Quality Analyst – GRG Health

Location: Pune, Maharashtra, India (On-site)

Experience: Freshers

Employment Type: Full-time | Hybrid after probation

About the Organisation

GRG Health (a Growman Group Company) is a global healthcare knowledge services and market research organisation with offices in Pune, Gurgaon, Bangalore, Boston (USA), and Singapore.

The company works with top international healthcare clients, combining traditional insights gathering with advanced data analytics and AI solutions.

Position Overview

GRG Health is hiring Market Research Quality Analysts to join its expanding healthcare research and analytics team.

This is a great opportunity for fresh graduates looking to build strong skills in research, communication, data quality, and healthcare analytics.

What You’ll Gain

• Opportunity to work with leading global healthcare clients

• Structured training by industry experts – no prior experience required

• Exposure to healthcare research, analysis, and quality control

• Supportive and high-energy work culture

• Hybrid work model after probation

• Fast-track career growth in the healthcare analytics industry

Who Can Apply

Education: Bachelor’s or Master’s degree in:

Biotechnology, Microbiology, Pharmacy, Bioinformatics, Life Sciences, or any related Science stream

Experience: Freshers only

Required Skills:

1. Strong English communication (written and verbal)

2. Basic knowledge of biotech, biomedical, or pharma concepts

3. Proficiency in MS Office (Word, Excel, PowerPoint)

4. Eagerness to learn, grow, and take initiative

5. Preferred: Basic understanding of Market Research (not mandatory)

Key Responsibilities

• Review market research content for quality, grammar, accuracy, and structure

• Suggest improvements and ensure deliverables meet client standards

• Collaborate with research teams to deliver high-quality healthcare insights

• Learn and support both primary and secondary research activities

Job Details

Locations: Pune / Gurgaon

Shift Timings:

Pune: 12 PM – 9 PM

Gurgaon: 11 AM – 8 PM

Mode: On-site during probation; Hybrid after 4 months

Bond: 1 Year

Openings: 17 (Immediate joiners preferred)

How to Apply

Send your updated CV to: tanya.thakare@martlenz.com

Subject line: Application for Market Research Quality Analyst – [Your Name]

Research Executive – QC / ARD (Bycus Therapeutics Pvt. Ltd.)

Location: Hyderabad, Telangana, India

Experience: Freshers and early-career candidates

Employment Type: Full-time | On-site

Advertisement No: BT/QC/RE/10-2025

About the Organisation

Bycus Therapeutics Pvt. Ltd. is a Hyderabad-based biotechnology company focused on the research, development, and manufacturing of high-quality, affordable biosimilars and biologics. The company is driven by innovation in R&D and is expanding its analytical and quality control capabilities to support its growing biologics pipeline.

Position Overview

Bycus Therapeutics is inviting applications for the position of Research Executive in its Analytical R&D (ARD) and Quality Control (QC) departments.

This role offers hands-on exposure to advanced analytical techniques used in biologics research and manufacturing.

Key Responsibilities

• Conduct HPLC analysis of recombinant proteins, peptides, and biological samples

• Perform routine maintenance and calibration of HPLC instruments

• Analyze in-process R&D and quality control samples

• Assist in method development and validation for HPLC-based assays

• Maintain accurate documentation and comply with laboratory quality standards

Eligibility Criteria

Education:

1. B.Pharm / B.Tech (Life Sciences, Chemistry, or Pharmacy) – Freshers eligible

2. B.Sc (Life Sciences / Chemistry) – up to 1 year of experience

Experience: Freshers encouraged to apply

Technical Skills: Basic understanding of analytical methods; prior HPLC experience not required

Number of Vacancies: 06

Why Join Bycus Therapeutics

• Exposure to biopharmaceutical R&D and quality control functions

• Learn analytical techniques in a regulated biotechnology environment

• Opportunity to build a foundation for a career in biosimilar and biologics research

How to Apply

Interested candidates can send their updated CV to:

Email: careers@bycusbio.com

Please mention the Advertisement Number (BT/QC/RE/10-2025) in the subject line of the email.

Market Research Analyst 

Location: Pune, Maharashtra, India (with hybrid option after probation)

Experience: Freshers only

Employment Type: Full-time | On-site (Hybrid after probation)

About the Organisation

GRG Health, a Growman Group company, is an award-winning global healthcare knowledge services and market research organisation.

Headquartered in Pune, India, with offices in Gurgaon, Bangalore, Boston (USA), and Singapore, GRG Health combines traditional market research with advanced AI-driven analytics to deliver strategic healthcare insights.

Job Overview

The Market Research Analyst will support healthcare market research and data analytics projects for global clients.

This role involves gathering insights, managing data, conducting interviews, and generating detailed market reports.

Key Responsibilities

• Conduct online market and business research on assigned healthcare topics

• Support in data analysis, insight generation, and report preparation

• Build and manage a market information database

• Identify and engage target professionals across EU and APAC regions for research interviews (via email and phone)

• Conduct qualitative and quantitative interviews with healthcare professionals

• Interpret collected data, develop insights, and contribute to final research deliverables

• Collaborate with internal teams for reporting and presentation

Qualifications

• Education: B.Sc / B.Tech / M.Sc / M.Tech (Biotechnology, Microbiology, Pharmacy, Life Sciences, or Healthcare streams)

• Experience: Freshers only

• Location: Pune or Gurgaon

• Probation Period: 4 months

• Bond: 1 year

• Shifts: Rotational (including night shifts)

• Hybrid Mode: Available after successful completion of probation

Required Skills

• Strong verbal and written communication skills

• Good analytical and critical thinking abilities

• Basic understanding of market research processes

• Ability to interpret data and manage multiple tasks efficiently

• Confidence in conducting professional interviews (telephonic or in-person)

About the Role

This position offers an excellent opportunity for fresh graduates to begin a career in healthcare market research.

GRG Health provides structured training, mentorship, and exposure to global healthcare projects powered by AI and data science.

Pfizer Hiring – Associate Safety Data Management Specialist

Pfizer is inviting applications for the role of Associate Safety Data Management Specialist.

This is an excellent opportunity for fresh pharmacy graduates to begin their career in Pharmacovigilance and Drug Safety.

Role Overview

The selected candidates will be responsible for processing and managing Individual Case Safety Reports (ICSRs) from both clinical trials and post-marketing sources using the ARGUS Safety Database. The position involves ensuring the accuracy, consistency, and regulatory compliance of safety data.

Key Responsibilities

• Review and validate ICSR information and perform duplicate checks

• Create and update safety cases in ARGUS as per standard procedures

• Identify and code products and adverse events

• Assess seriousness, causality, and listedness of reported events

• Draft clear and concise case narratives

• Determine necessary follow-up information

• Perform quality checks to ensure technical and regulatory accuracy

Eligibility Criteria

• Education: B.Pharm, M.Pharm, or Pharm.D

• Experience: Freshers only

• Strong analytical skills and attention to detail

• Good written and verbal communication skills

• Ability to work collaboratively in a team-oriented environment

• Willingness to learn and grow in a global pharmaceutical setting

Preferred Qualifications

1. Certification or coursework in Pharmacovigilance

2. Understanding of medical terminology and international drug safety regulations

3. Prior publications or research experience in peer-reviewed journals

About Pfizer

Pfizer is a global leader in healthcare innovation, dedicated to discovering, developing, and delivering breakthrough therapies that improve patient lives worldwide.

Technical Reporting Associate I – Entry Level

About the Role:

Join Labcorp’s Global Reporting Solutions team as a Technical Reporting Associate I. This entry-level role provides hands-on experience supporting non-clinical studies and producing high-quality study reports. You’ll learn industry-standard reporting practices while gaining exposure to diverse study designs.

Key Responsibilities:

• Learn and use software tools including word processors, spreadsheets, table-generation programs, collaboration platforms, and databases.

• Prepare, draft, and review data tables for non-clinical study updates, including basic statistical analyses.

• Assist in generating CTD tabulated summaries for study reports.

• Perform manual data entry and transfer data between MS Excel and MS Word for report inclusion.

• Conduct quality control checks on tables and reports to ensure accuracy and consistency.

• Organize and schedule your workload to meet deadlines, communicating proactively with team members and supervisors.

• Mentor new associates and provide peer review support after sufficient training.

• Develop proficiency in additional reporting-related duties as assigned.

Why Labcorp:

Labcorp is committed to inclusion, diversity, and equal opportunity. We make employment decisions based on merit and business needs, without regard to race, gender, religion, disability, or any legally protected characteristic. We welcome all qualified applicants and provide support for individuals with disabilities during the application process.

Elanco (Bangalore, India)

About Elanco

Elanco (NYSE: ELAN) is a global leader in animal health, dedicated to innovation and delivering products and services that prevent and treat diseases in farm animals and pets. Guided by our purpose “Go Beyond for Animals, Customers, Society, and Our People”, we foster a diverse, inclusive, and collaborative work environment where creativity, innovation, and learning thrive.

Role Overview

The Analyst – Pharmacovigilance (PV Case Processing) is responsible for managing adverse event reports, ensuring data accuracy, and maintaining compliance with global PV regulations and timelines. This entry-level role is ideal for fresh graduates seeking to build a career in pharmacovigilance and animal health research.

Key Responsibilities

• Data entry and management of adverse event reports in the PV database.

• Assess seriousness and causality of adverse events.

• Ensure completeness, quality, and regulatory compliance of cases for submission.

• Identify and escalate issues in case processing to avoid submission delays.

• Comply with internal and external timelines for adverse event and product complaint case management.

• Develop knowledge of global pharmacovigilance regulations and processes.

Minimum Qualifications

1. Bachelor’s or Master’s degree in a related field.

2. 0–1 year of experience; basic understanding of medical terminologies and adverse event reporting.

Preferred Qualifications

• Strong verbal and written communication skills.

• Ability to manage multiple priorities and products simultaneously.

• Effective collaboration with coworkers, managers, and stakeholders.

• Knowledge of global and local pharmacovigilance regulations.

Additional Information

Travel: 0%

Location: Bangalore, India

Elanco encourages applicants from diverse backgrounds and experiences, even if not all qualifications are met.

Elanco is an EEO/Affirmative Action Employer, committed to diversity, equity, and inclusion in the workplace.

Associate Medical Writer | Red Nucleus (US – Remote / Office)

About Red Nucleus

Red Nucleus is a global leader in strategic learning, medical communications, and scientific advisory services for the life sciences industry. With nearly 1,000 employees worldwide, we are committed to creativity, quality, and timely delivery. Recognized internationally as a “Great Place to Work”, we foster a culture of innovation, community, and meaningful work.

Role Overview

As an Associate Medical Writer, you will contribute to medical communications projects across therapeutic areas. You will create, edit, proofread, and manage scientific content for multiple formats, including newsletters, articles, slide decks, eLearning modules, and web applications. You will work closely with the Medical Director and Account Leads to provide strategic recommendations that support client brand goals.

This is a developmental role with significant opportunities for growth, skill-building, and exposure to global clients.

Key Responsibilities

• Conduct research, fact-check, and secure references for assigned topics.

• Support the Medical Services Team in developing, writing, and editing content to meet deadlines.

• Assist in client meetings, regulatory submissions, and review processes.

• Maintain up-to-date knowledge of medical trends, terminology, and industry standards.

• Apply creative and critical thinking to resolve content or project-related issues.

• Exhibit professionalism, adaptability, and dedication to exceptional client service.

Skills & Qualifications

• Advanced degree in pharmacy, pharmaceutical sciences, nursing, or biosciences preferred.

• Entry-level experience in clinical content development or medical writing preferred.

• Strong writing skills, medical terminology knowledge, and attention to detail.

• Proficiency in Microsoft Office (Word, Excel, PowerPoint, Outlook).

• Strong organizational, time management, and prioritization skills.

• Self-starter with the ability to work independently or as part of a team.

• Willingness to travel occasionally (10–25% overnight).

Why You’ll Love Working at Red Nucleus

1. Competitive pay, benefits, wellness programs, and retirement plans.

2. Generous paid time off and flexible work arrangements.

3. Professional development, transfer opportunities, and performance-driven environment.

4. Inclusive, diverse, and people-first culture celebrating milestones, diversity, and community involvement.

5. Opportunities for remote work or office-based engagement in Yardley, US.

Red Nucleus is committed to equal employment opportunity and fosters a culture of diversity, equity, and inclusion.

Business Analyst – Corporate Strategy | FDC Limited (Mumbai)

Location: Corporate Office, Mumbai

Experience: 0–2 years

Qualification: CA or B.Pharm + MBA (Strategy / Finance / Healthcare preferred)

About the Opportunity

FDC Limited is seeking a Business Analyst to join their Corporate Strategy Team. This is an exciting opportunity for fresh graduates or early-career professionals to gain hands-on experience in strategic research, business analysis, and project execution within the pharmaceutical industry.

Key Responsibilities

• Conduct in-depth research on industry trends, competitors, and market dynamics.

• Support strategy presentations, financial models, and business planning.

• Assist in project feasibility analysis and monitor progress of cross-functional projects.

• Contribute to business development initiatives, partnerships, and M&A activities.

• Work closely with senior leaders to provide actionable insights for strategic decision-making.

Skills & Qualifications

• CA or B.Pharm with MBA (preferably in Strategy, Finance, or Healthcare).

• 0–2 years of relevant experience (internships or projects in pharma/healthcare a plus).

• Strong analytical and problem-solving skills.

• Proficiency in Excel and PowerPoint.

• Excellent communication skills and attention to detail.

• Proactive, collaborative, and eager to learn in a fast-paced environment.

How to Apply

Interested candidates can share their updated CV with the following details:

1. Total Experience

2. Current Designation

3. Current CTC

4. Expected CTC

5. Notice Period

📧 Send your profile to: harshal.jain@fdcindia.com

Subject Line: Business Analyst

Kickstart your career in pharmaceutical strategy and make an impact with FDC Limited.

Associate Healthcare Rsearch & Data Analyst

About the Opportunity

Join a dynamic and growing Biopharma Insights team within a leading Life Science and Healthcare Products organization. This role offers an exciting opportunity for recent postgraduates and early-career professionals to gain hands-on experience in market research, analysis, and forecasting across the pharmaceutical, biotechnology, and healthcare industries.

Key Responsibilities

• Conduct primary and secondary market research to analyze and interpret complex clinical and commercial datasets.

• Translate research insights into comprehensive market intelligence reports and forecasts.

• Design and execute primary research surveys and expert interviews in selected therapeutic areas.

• Evaluate market trends, opportunities, and competitive landscapes to support strategic decision-making.

• Prepare high-quality written deliverables, presenting insights clearly and objectively.

Skills & Qualifications

• Master’s degree in Pharmacy, Life Sciences, or Pharmaceutical Management (mandatory).

• 0–2 years of relevant experience in biopharma, healthcare, market research, or financial analysis.

• Strong understanding of at least one therapeutic area.

• Excellent communication and writing skills in English.

• Strong analytical mindset with attention to detail.

• Proficiency in MS Office (Word, Excel, PowerPoint).

Preferred Attributes

• Experience collaborating with global stakeholders.

• Flexible, collaborative, and able to perform under tight deadlines.

• Enthusiasm to learn, research, and grow within the life sciences domain.

About the Team

The Biopharma Insights team provides cutting-edge market analytics and research to global pharmaceutical, biotech, and healthcare companies. Analysts work on strategic planning, competitive intelligence, and market development projects—helping clients make data-driven decisions about new drug development and product management.

If you’re passionate about biopharma research, market analysis, and global healthcare insights, this is the perfect opportunity to launch your career in the life sciences industry.

Clinical Research Coordinators (CRC)

About the Job

We are looking for passionate Clinical Research Coordinators (CRC) to join our growing team. This is an exciting opportunity for fresh graduates with a clinical research course or background in life sciences/pharmacy who want to build a career in clinical trials and research.

Position Details

Role: Clinical Research Coordinator

Location: Delhi

Employment Type: Full-time

Experience: Freshers with clinical research training or related background encouraged to apply!

Key Responsibilities

• Conduct clinical trials in compliance with ICH GCP and protocol guidelines.

• Support study start-up activities and assist with site initiation.

• Participate in recruitment and retention of study subjects.

• Complete and maintain source documents, CRFs, and logs accurately.

• Compile and update the Site Master File.

• Manage Investigational Products (IP), including accountability and shipping.

• Coordinate submissions and communication with the Ethics Committee.

• Update sponsors on study progress and prepare for monitoring visits.

• Perform other responsibilities assigned by management.

Who Can Apply

• Freshers with a completed Clinical Research course.

• Graduates/postgraduates in Life Sciences, Pharmacy, Biotechnology, or related fields.

• Strong interest in clinical trials and regulatory compliance.

• Excellent organisational, communication, and documentation skills.

Why Join Us?

• Gain hands-on experience in clinical trials.

• Learn directly from experienced professionals.

• Be part of innovative projects that shape the future of healthcare.

• A great opportunity to grow your career in clinical research.

Regulatory Affairs Associate I (Regulatory Operations – Data Analytics)

About the Role

We are looking for a Regulatory Affairs Associate I specializing in Regulatory Data Analytics to join our Global Regulatory Operations (GRO) team. In this role, you will manage and maintain product registration data to ensure compliance with global regulatory standards such as xEVMPD and Article 57.

You will play a key role in ensuring data accuracy, integrity, and availability across Teva’s Global Regulatory Affairs systems — supporting both operational and strategic initiatives related to regulatory data management.

Key Responsibilities

• Execute daily operations in accordance with SOPs and Work Instructions related to regulatory data analytics and product registration.

• Extract, verify, and manage regulatory data from source documentation and dossiers, ensuring compliance and completeness.

• Perform quality control and data integrity checks for global registration databases.

• Collaborate effectively with cross-functional Global Regulatory Affairs teams to align data requirements and reporting standards.

• Contribute to data quality improvement initiatives, system integrations, and technology transformation projects.

• Serve as a subject matter expert (SME) for regulatory data structures, workflows, and systems.

Desired Qualifications

• Bachelor’s or Master’s degree in Pharmacy (B.Pharm / M.Pharm) — mandatory.

• 1–3 years of relevant experience in Regulatory Affairs or Regulatory Operations within the pharmaceutical industry.

• Strong understanding of regulatory dossiers, submission structures, and registration data models.

• Experience with Regulatory Information Management (RIM) systems is preferred.

• Excellent attention to detail, analytical skills, and ability to manage data with precision.

Why Join Us

1. Opportunity to work on global regulatory projects impacting healthcare compliance worldwide.

2. Exposure to advanced regulatory data management systems and cross-functional collaboration.

3. Continuous learning environment fostering career growth in Regulatory Operations & Data Analytics.

Life Science Intern (Paid | AI-Driven Drug Development & Clinical Research) – On-Site, Pune

Location: Pune, India

Type: Paid Internship (with potential for full-time conversion)

Company: Dizzaroo Pvt. Ltd.

About Dizzaroo

Dizzaroo Pvt. Ltd. is the R&D innovation hub of the Dizzaroo Group — an AI-driven life sciences company developing intelligent solutions for clinical research, translational biology, and oncology. Our work spans across clinical data review automation, protocol authoring, digital pathology, and AI knowledge graphs, enabling faster and smarter drug development.

About the Role

We’re looking for a Life Science Intern to contribute as a domain expert in our AI research and development projects focused on drug discovery and clinical research.

This is an on-site role based in Pune, ideal for final-year students or recent graduates seeking hands-on experience and a potential full-time opportunity.

Key Responsibilities

• Support the design and training of AI models for life science applications.

• Work with biomedical and clinical datasets (preclinical, translational, and clinical).

• Develop workflows bridging biological insights with AI and computational pipelines.

• Participate in data curation, annotation, and interpretation throughout the drug development lifecycle.

• Collaborate closely with data science and engineering teams on R&D initiatives.

• Prepare concise documentation and present findings to the internal team.

Who Can Apply

• Students or graduates in Life Sciences, Biotechnology, Pharmacology, Bioinformatics, or related fields.

• Strong fundamentals in molecular biology, pharmacology, or clinical research.

• Eager to learn and comfortable working across biology, data, and AI domains.

• Good communication and analytical skills.

• (Bonus) Familiarity with Excel, Python/R, or drug development workflows.

Medical & Scientific Writer Jobs – NeoCrest Life Sciences Consulting (Remote) 

NeoCrest Life Sciences Consulting is inviting applications for the position of Medical & Scientific Writer. This is an exciting remote opportunity for life sciences and pharma professionals to work with a leading global consulting firm and contribute to high-quality scientific publications and regulatory documentation.

About NeoCrest Life Sciences Consulting

NeoCrest is a global leader in life sciences consulting, specializing in medical writing, regulatory affairs, and scientific communications. The company delivers impactful solutions for pharmaceutical companies, clinical research organizations, and healthcare providers.

Job Role: Medical & Scientific Writer

Location: Remote

Experience Required: 1–6 years

Salary: ₹4,00,000 – ₹8,00,000 per annum (depending on experience and qualifications)

Employment Type: Full-time, Remote

Key Responsibilities

• Draft, edit, and review scientific manuscripts such as original research articles, review papers, case reports, and systematic reviews.

• Prepare clinical trial documentation and regulatory reports.

• Develop medical and regulatory affairs content.

• Create medico-marketing collaterals, presentations, and training materials.

• Ensure scientific accuracy, compliance with guidelines, and high-quality deliverables.

Required Qualifications

• M.Pharm, M.Sc., PhD, MBBS, MD, or equivalent degree in life sciences, pharmacy, or medical sciences.

• 1–6 years of experience in medical/scientific writing (manuscripts, regulatory writing, publications).

• Strong skills in scientific literature search, reference management, and data interpretation.

• Familiarity with tools such as EndNote, Mendeley, Zotero, or statistical analysis software (preferred).

• Excellent writing, editing, and presentation skills.

Why Join NeoCrest?

• Work remotely with a leading global life sciences consulting firm.

• Engage in high-impact scientific writing and publication projects.

• Collaborate with expert researchers and healthcare professionals.

• Competitive salary with growth and learning opportunities.

How to Apply

Interested candidates should send their CV and relevant details to:

Email: jatin.y@neocrest.in

Subject Line: Application – Medical/Scientific Writer

Required Application Details:

1. Years and areas of medical/scientific writing experience

2. Published papers (primary author/co-author)

3. Types of papers handled (research articles, reviews, case reports, etc.)

4. Current and expected CTC

5. Highest qualification (degree, university, year)

6. Notice period/availability

7. Additional skills (statistics, regulatory writing, reference software, presentations)

Only complete applications will be considered.

IQVIA Hiring 2025

IQVIA, a global leader in healthcare data and technology solutions, is hiring for Clinical Data Management positions in Pune, Maharashtra. This is a great opportunity for experienced professionals in clinical research and data management to work with one of the most respected names in the healthcare industry.

About IQVIA

IQVIA is a pioneer in the application of advanced analytics, technology solutions, and contract research services to the life sciences industry. Their expertise in clinical data management helps improve healthcare outcomes worldwide.

Job Title: Associate Data Team Lead (R1505063)

Location: Pune, Maharashtra

Employment Type: Full-time, Hybrid

Experience Required: 6+ years

Education: Bachelor’s Degree (Life Sciences, Pharmacy, or relevant fields preferred)

Key Responsibilities

• Manage end-to-end clinical data management processes, including protocol review, CRF design, and database lock.

• Develop and implement data management plans and related study documents.

• Oversee and coordinate with Clinical Data Management vendors.

• Use Electronic Data Capture (EDC) systems — Medidata RAVE preferred, Oracle Clinical experience is an advantage.

• Analyze query trends and protocol deviations to ensure data integrity.

• Author and review documents such as Data Quality Management Plans and eCRF Completion Guidelines.

• Ensure compliance with FDA and ICH guidelines.

• Lead or support Health Authority inspections and audits.

• Mentor and manage team members for quality and efficiency.

Qualifications

• Bachelor’s degree in Life Sciences, Pharmacy, or related field (preferred).

• Minimum 6 years of experience in clinical data management.

• Strong knowledge of clinical drug development process and regulatory guidelines (FDA, ICH).

• Excellent analytical, communication, and leadership skills.

• Experience working with multi-disciplinary teams and external vendors.

Why Join IQVIA?

• Work with a global leader in clinical research and healthcare analytics.

• Exposure to cutting-edge clinical data management technologies.

• Career growth opportunities with continuous learning.

• Collaborative and inclusive work culture.

Medusind Solutions Hiring 2025

Medusind Solutions is inviting applications for the position of Content Analyst – Non-Clinical in Mumbai. This is a fantastic opportunity for fresh graduates and professionals with up to 2 years of experience to join a leading healthcare content management company.

About Medusind Solutions

Medusind Solutions is a global leader in healthcare data management and content services. The company specializes in delivering high-quality medical and laboratory product data to global healthcare organizations.

This is an exciting opportunity for candidates who want to build a career in medical content research and data management.

Job Role: Content Analyst – Non-Clinical

Location: Mumbai (Hybrid)

Experience: 0–2 Years (Freshers welcome)

Salary: ₹2.5 LPA – ₹4.5 LPA

Vacancies: 20

Key Responsibilities

• Research, validate, and update product information for medical and laboratory diagnostics.

• Categorize products into appropriate taxonomy groups using global classification standards.

• Attribute specifications, features, and metadata to products.

• Ensure accuracy, completeness, and consistency of product data.

• Perform quality checks and maintain data integrity.

• Coordinate with suppliers and internal teams for updates.

Qualifications

Eligible candidates should possess one of the following degrees:

• M.Sc. in Microbiology / Biotechnology / Pharmacy

• BHMS / BDS / BAMS / BSMS

• BPT / MPT

Why Join Medusind Solutions?

• Exposure to medical content management in a global company.

• Career growth opportunities in the healthcare domain.

• Work with expert teams in a dynamic environment.

• Learn and grow with cutting-edge healthcare data technology.

Walk-In Interview Details

Dates: 30th September – 9th October 2025

Time: 12:00 PM – 4:00 PM

Venue:

4th Floor, The Great Oasis, D13, Street 21, Shree Krishna Nagar,

Marol MIDC Industry Estate, Andheri East, Mumbai, Maharashtra – 400093

Contact: Ms. Nayana Chavan – +91 8928289807

How to Apply

Interested candidates can attend the walk-in interview directly with their updated CV, educational certificates, and valid ID proof.

Strava Healthcare Hiring 2025 – HR, Accounts & Production Jobs in Ahmedabad (0–7 Years Experience)

Strava Healthcare Pvt. Ltd. is inviting applications from talented professionals and fresh graduates for multiple openings in HR, Accounts, and Production departments. The company is one of the fast-growing pharmaceutical manufacturers based in Ahmedabad, Gujarat, offering excellent opportunities for both freshers and experienced candidates.

About Strava Healthcare

Strava Healthcare Pvt. Ltd. is a reputed name in the Indian pharmaceutical industry, focused on the production of tablets and capsules under strict GMP standards. The company provides a dynamic workplace environment with an emphasis on innovation, quality, and career growth.

Current Job Openings – October 2025

1. HR – Trainee Officer

Qualification: MBA, BBA, M.Com, or B.Com

Experience: 0–2 Years (Freshers can apply)

Responsibilities:

• Assist in recruitment, onboarding, and employee engagement activities

• Manage HR documentation and statutory compliance

• Support training and development programs

2. Accounts – Senior Executive

Qualification: M.Com / B.Com

Experience: 4–7 Years

Responsibilities:

• Maintain ledgers, balance sheets, and accounting records

• Handle budgeting, auditing, and taxation processes

• Prepare and analyze financial reports

3. Production – Officer

Qualification: M.Sc / B.Pharm

Experience: 1–3 Years

Responsibilities:

• Supervise OSD (Tablets/Capsules) manufacturing operations

• Ensure compliance with GMP and company SOPs

• Coordinate with QA/QC departments

4. Production Operators

Qualification: ITI

Experience: 1–5 Years

Departments: Compression, Granulation, Strip, Coating, Blister, Capsule

Responsibilities:

• Operate and maintain production machinery

• Follow GMP and safety guidelines

• Ensure quality consistency and timely production

Why Join Strava Healthcare?

• Competitive salary based on experience and skill level

• Excellent career growth and learning opportunities

• Employee welfare and health benefits

• Exposure to a reputed pharmaceutical manufacturing setup

Walk-In Interview Details

Dates: October 7, 2025 (Tuesday)

Time: 9:00 AM – 4:00 PM

Venue:

Strava Healthcare Pvt. Ltd.

Survey No. 135P, Bavla–Sanand Road,

Village Lodariyal, Taluka Sanand, Ahmedabad, Gujarat – 382220

Phone: +91 9512660923

Note: Bring an updated CV, educational certificates, and valid ID proof for verification.

Hiring Now: Pharmacists & Senior Pharmacists | Kolkata & Nearby Locations!

Are you a qualified Pharmacist looking for a job in Kolkata? Tata 1mg, one of India’s leading digital health platforms, is hiring Pharmacists and Senior Pharmacists to manage its rapidly growing offline stores in Kolkata, Bardhaman, and other key locations.

With over 100 job openings, this is your chance to join a trusted healthcare brand and contribute to making healthcare more accessible, affordable, and reliable for millions of Indians.

Job Responsibilities:

• Oversee daily pharmacy store operations and ensure smooth functioning.

• Drive sales performance and meet revenue targets.

• Lead, train, and motivate the team to deliver exceptional customer service.

• Manage inventory, stock replenishment, and merchandising.

• Ensure compliance with company policies and operational standards.

Qualifications & Skills:

• Bachelor’s degree in Pharmacy or related medical field.

• Prior experience in pharmacy store management preferred.

• Strong leadership, organizational, and communication skills.

• Ability to multitask and work efficiently under pressure.

• Proficiency in MS Excel and knowledge of the pharmaceutical industry.

Benefits of Working at Tata 1mg:

• Competitive salary (INR 2.5 LPA – 4.8 LPA).

• Fast-track career growth opportunities.

• Exposure to India’s leading healthcare retail and e-pharmacy platform.

• Work with a dedicated team impacting millions of lives.

Contact: 7688839032

Medical Coding Internship for Freshers at Predix Healthcare Solutions – Hyderabad

Are you a fresher looking to start your career in medical coding? Predix Healthcare Solutions, a leading healthcare company in Hyderabad, is inviting graduates from Life Sciences, Pharmacy, Nursing, and related fields to join as Medical Coding Interns. This is a great opportunity to gain hands-on experience, work with senior professionals, and build a strong career in the fast-growing healthcare and medical coding industry.

Internship Details

Company: Predix Healthcare Solutions

Location: Hyderabad, Telangana

Position: Medical Coding Intern

Eligibility: Freshers and candidates with up to 3 years of experience

Academic Background: Life Sciences, Pharmacy, Nursing, Biotechnology, or related fields (2023, 2024, 2025 pass-outs)

Certification: CPC-A, CCA, or non-certified candidates can apply

Responsibilities

As a Medical Coding Intern, you will:

• Assign accurate ICD-10-CM and CPT codes for diagnoses and procedures

• Ensure compliance with coding guidelines and regulatory standards

• Assist in reviewing and processing medical claims

• Work with software tools for coding and data management

• Collaborate with senior coders to resolve discrepancies

• Maintain patient confidentiality and follow HIPAA regulations

Skills Required

• Knowledge of ICD-10-CM and CPT coding systems

• Basic computer skills (MS Office, data entry, etc.)

• Strong attention to detail and willingness to learn

Benefits of Joining

• Real-time hands-on training in medical coding

• Guidance from experienced industry mentors

• Opportunity for a full-time job offer after internship

• Boost your resume with industry-recognized experience

• Skill development in a structured program

Why Choose Medical Coding as a Career?

Medical coding is one of the most in-demand healthcare professions in India and abroad. With the growing need for accurate health data management, certified coders are in high demand across hospitals, insurance companies, and healthcare BPOs. Starting your career with Predix Healthcare Solutions gives you an edge to grow in this field.

Pharma Executive Jobs at Bafna Pharmaceuticals – Chennai

Bafna Pharmaceuticals Ltd., a globally accredited pharmaceutical exporter with MHRA certification, is inviting applications for Production Executive roles in Chennai. This is an excellent opportunity to advance your career in pharmaceutical manufacturing while working with one of India’s trusted pharma companies.

Why Join Bafna Pharmaceuticals?

• Work with an MHRA-approved, globally recognized pharma company

• Build expertise in pharmaceutical production and quality systems

• Long-term growth opportunities in a stable, innovation-driven environment

How to Apply

Interested candidates can apply by sending their updated CV to:

Email: hrsupport@bafnapharma.com

Subject Line: Application for Production Executive – Redhills Chennai

Documents to Attach

• Updated Resume

• Offer / Increment Letters

• Last 3 Months’ Payslips & Bank Statement

• Previous Service Letters

• Educational Certificates

• Aadhaar & PAN Card

Contact for Queries

Mr. Gopalakrishnan – +91-7708274886

For more information about our MHRA-accredited operations, visit www.bafnapharma.com.

Note: Applications are being accepted on an urgent basis. Positions will remain open until filled. Apply now for pharma executive jobs in Chennai with Bafna Pharmaceuticals.

AR&D – API Jobs for Freshers & Experienced in Hyderabad

Biophore, a leading pharmaceutical research and development organization, has announced a walk-in interview drive for positions in its AR&D – API department. This recruitment drive is open for both freshers and experienced candidates.

• Date: 27th September 2025 (Saturday)

• Time: 10:00 AM – 03:00 PM

• Venue: Biophore R&D Centre, Pashamylaram, Hyderabad

Available Positions

1. Trainees (Freshers)

• Qualification: M.Sc. / B. Pharmacy / M. Pharmacy (Analysis)

• Experience: 0 – 1 year

• Key Skills Required:

• Knowledge of analytical instruments such as HPLC and GC

• Basic understanding of method validation

• Strong academic background and communication skills

2. Jr. Research Analyst / Research Analyst (Only Males)

• Qualification: M.Sc. / B. Pharmacy / M. Pharmacy (Analysis)

• Experience: 1 – 3 years

• Key Skills Required:

• Analytical method development and validation

• Hands-on experience with HPLC, GC, GCMS, LCMS

Documents Required for Walk-in Interview

Candidates attending the interview must carry the following:

• Updated CV/Resume

• Educational certificates (xerox copies)

• PAN & Aadhaar card

• Last 3 months’ payslips or 6 months’ bank statements

Application Process

Interested candidates can attend the walk-in interview at the Biophore R&D Centre, Pashamylaram, Hyderabad on 27th September 2025 between 10:00 AM and 03:00 PM.

For candidates unable to attend in person, profiles may be sent via email to: recruitments@biophore.com

About Biophore

Biophore India Pharmaceuticals Pvt. Ltd. is a research-driven pharmaceutical company specializing in the development of niche APIs and advanced intermediates. With a strong emphasis on regulatory compliance, quality, and innovation, Biophore provides solutions catering to global pharmaceutical requirements.

Official Website: www.biophore.com 

Clinical Data Associate at Avance Clinical – Bengaluru, Karnataka

Avance Clinical, a leading global Contract Research Organisation (CRO), is seeking a Clinical Data Associate to join its Bengaluru office. This full-time, on-site position is ideal for candidates with 2–3 years of experience in clinical research, data management, and GCP-compliant environments. The role offers an excellent opportunity for professionals looking to advance their career in the pharmaceutical and clinical research industry.

About the Role

The Clinical Data Associate will play a critical role in managing, validating, and reviewing clinical trial data to ensure accuracy, compliance, and high-quality deliverables. The position involves collaboration with cross-functional teams and direct involvement in key aspects of clinical data management and reporting.

Key Responsibilities

• As a Clinical Data Associate at Avance Clinical, your responsibilities will include:

• Developing and reviewing Case Report Forms (CRFs) and completion guidelines.

• Preparing Data Management Plans and supporting edit check documentation.

• Validating databases using dummy data and SAS outputs.

• Performing data review, discrepancy resolution, and query management.

• Assisting with MedDRA / WHO-DD coding under mentor guidance.

• Conducting quality control checks prior to database lock.

• Archiving study documentation, including Medrio files.

• Supporting filing, reconciliation, and CRF tracking processes.

• Collaborating effectively with cross-functional teams to meet study timelines and regulatory standards.

Required Qualifications and Skills

Candidates should meet the following criteria:

• Bachelor’s degree in Life Sciences, Pharmacy, or a related discipline.

• 2–3 years of experience in a CRO or pharmaceutical industry, working under GCP compliance.

• Strong knowledge of ICH-GCP guidelines, clinical trial processes, and medical terminology.

• Hands-on experience in data entry, discrepancy management, and data validation.

• Excellent time management, communication, and organizational skills.

• Proficiency in MS Office Suite and the ability to work independently.

Benefits of Joining Avance Clinical

Joining Avance Clinical provides a unique opportunity to work with a globally recognized CRO and gain exposure to innovative drug development projects. Employees benefit from a supportive and collaborative work environment, professional growth opportunities through training and mentorship, and the chance to contribute to high-impact clinical research initiatives.

This position is ideal for detail-oriented professionals who are passionate about clinical trials and want to expand their expertise in clinical data management within a dynamic and globally recognized organization.

Location: Bengaluru, Karnataka

Employment Type: Full-time, On-site

Avance Clinical offers a platform to grow your career in clinical research while contributing to meaningful and impactful drug development projects.

Pharmacovigilance Internship at ProPharma – Hyderabad

ProPharma, a global leader in regulatory sciences and drug safety solutions, is offering an exciting Pharmacovigilance Internship in Hyderabad. This 12-month, on-site internship provides an exceptional opportunity for graduates to gain hands-on experience in pharmacovigilance, drug safety, and regulatory compliance. Aspiring professionals will be trained in real-world case management and Argus safety database operations, preparing them for a successful career in the pharmaceutical and life sciences industries.

About the Internship

This internship is designed for Pharmacy, Life Sciences, and Medicine graduates who are eager to develop practical skills in pharmacovigilance and drug safety. Interns will work closely with experienced professionals and gain exposure to global pharmacovigilance standards, safety reporting processes, and regulatory requirements.

Key Responsibilities

• As a Pharmacovigilance Intern at ProPharma, you will:

• Manage pharmacovigilance mailboxes, including triaging client communications and safety reports.

• Conduct duplicate searches and perform initial case book-in as required.

• Enter critical case information such as patient details, drug information, and adverse events into the Argus safety database.

• Assist in case processing, narrative writing, and MedDRA coding to ensure accurate documentation.

• Support Individual Case Safety Report (ICSR) management to meet stringent regulatory timelines.

• Collaborate with cross-functional teams to ensure timely reporting of adverse events.

• Maintain compliance with pharmacovigilance standards and documentation protocols.

Eligibility Criteria

Candidates applying for this internship should meet the following qualifications:

• Completed degree in Pharmacy, Life Sciences, Medicine, or related fields.

• Basic knowledge or prior experience with Argus database.

• Understanding of pharmacovigilance principles and drug safety compliance.

• Proficiency in Microsoft Office applications including Word, Excel, and PowerPoint.

• Strong written and verbal communication skills.

• Attention to detail and the ability to work effectively in a fast-paced environment.

Benefits of Joining ProPharma

Interns at ProPharma will receive practical training in global pharmacovigilance case processing and gain exposure to real-world ICSR handling. The program provides mentorship from experienced PV professionals and offers a clear pathway to building a career in drug safety and regulatory affairs. ProPharma also fosters an inclusive and diverse work environment that encourages innovation, professional growth, and continuous learning.

This internship is an excellent opportunity for motivated graduates to gain in-depth knowledge of pharmacovigilance operations, regulatory compliance, and drug safety practices. Joining ProPharma will provide a strong foundation for a career in the pharmaceutical industry while working in a globally recognized organization.

Location: Hyderabad, India

Internship Duration: 12 months

Mode: Work-from-office

Apply today to begin your journey in pharmacovigilance and gain hands-on experience that will enhance your career prospects in the pharmaceutical and life sciences sectors.

Hybrid Pharmacovigilance Jobs for Freshers 2025

Fortrea, a leading global clinical research and life sciences company, is inviting applications for the role of Assistant I – PSS (Pharmacovigilance & Safety Services) at its Pune office. This is a full-time hybrid job opportunity ideal for freshers and early-career professionals who want to start their careers in pharmacovigilance, clinical safety, and regulatory compliance.

This position offers hands-on experience in safety reporting, adverse event management, and clinical research operations, making it a valuable entry point for graduates looking to build their careers in the pharmaceutical industry.

Job Details

• Position: Assistant I – PSS (Pharmacovigilance & Safety Services)

• Location: Pune (Hybrid work model)

• Job Type: Full-time

• Application Deadline: October 6, 2025

• Job Requisition ID: 254803

Job Overview

As an Assistant I – PSS, you will play a critical role in clinical safety operations, supporting both clinical trials and post-marketing surveillance. Your responsibilities will include handling adverse event (AE/SAE) reports, ensuring accurate data entry, preparing narratives, and submitting safety reports to regulatory authorities and clients within strict timelines.

This role is well-suited for graduates in life sciences, pharmacy, nursing, or related fields who want to gain practical exposure in pharmacovigilance, regulatory submissions, and safety data management.

Key Responsibilities

• Intake, triage, and processing of safety information and case reports

• Enter adverse event data into safety tracking systems

• Draft patient narratives and code safety events using MedDRA

• Conduct listedness assessments for marketed products

• Generate and manage safety queries, liaising with medical staff to resolve discrepancies

• Submit expedited SAE reports to regulators, clients, investigators, and stakeholders

• Support database reconciliation and periodic safety update reports (PSURs)

• Ensure compliance with SOPs, global regulatory requirements, and quality systems

• Archive safety-related documents and maintain proper records

• Collaborate with cross-functional teams to support client projects

Qualifications

• Fortrea accepts candidates with a wide range of educational backgrounds. Equivalent industry experience may be considered.

• Non-Degree Holders: 6 months – 1 year of safety or relevant experience

• Associate Degree: 0–6 months of safety or relevant experience

• BS/BA (Life Sciences, Pharmacy, Nursing, Medical Sciences, or related field): 0–6 months of safety or relevant experience

• MS/MA (Life Sciences, Pharmacy, Nursing, Medical Sciences, or related field): 0 years of experience required

• PharmD: 0 years of experience required

Relevant experience includes roles in pharmacovigilance, clinical research, medical affairs, clinical data entry, data management, regulatory affairs, or quality assurance.

Skills Required

• Strong attention to detail and accuracy in data handling

• Good written and verbal communication skills

• Ability to collaborate effectively in a team environment

• Proficiency in MS Office applications

• Analytical ability to manage and proofread numerical data

Why Join Fortrea?

Fortrea provides a global platform for professionals to develop careers in pharmacovigilance, safety services, and clinical research operations. As part of its growing team, you will contribute to:

• Ensuring patient safety in clinical trials and marketed products

• Regulatory compliance across multiple regions

• Exposure to global projects in pharmacovigilance and clinical researh

• Professional growth opportunities in the pharmaceutical and CRO industry

How to Apply

Eligible candidates can apply for this role through Fortrea’s official career portal before the deadline. Ensure your resume highlights relevant qualifications, subject knowledge, and interest in pharmacovigilance and safety services.

Last Date to Apply: October 6, 2025

Quality Control (QC) Roles at Taloja MIDC, Panvel | 21–22 September 2025

Are you a skilled professional in pharmaceutical quality control looking to take the next step in your career? Flamingo Pharmaceuticals Ltd, a leading pharmaceutical company in India, is hiring Senior Officers, Officers, Executives, and Analysts for its Quality Control (QC) Department at Taloja MIDC, Panvel.

This is your opportunity to join a trusted and fast-growing pharmaceutical organization, working in a regulatory-compliant environment. Walk-in interviews will be held on 21–22 September 2025.

Quality Control Job Responsibilities

As part of the QC team at Flamingo Pharmaceuticals Ltd, you will be responsible for ensuring product quality and compliance with international standards. Key duties include:

• Analysis & Testing: Perform testing of raw materials, packing materials, in-process samples, finished products, and stability samples as per GLP, GMP, and SOP guidelines.

• Method Validation & Transfer: Execute method validation and transfer activities to ensure reliability and accuracy.

• Regulatory Compliance: Work in compliance with MHRA, WHO, cGMP, GLP, and GDP standards.

• Documentation: Maintain accurate and complete documentation following Good Documentation Practices (GDP).

• Instrument Handling: Operate advanced analytical instruments such as HPLC, GC, UV-Vis Spectrophotometer, IR, KF, Potentiometer, pH Meter, and AAS.

Candidate Qualifications & Skills

To qualify for these QC positions, applicants must meet the following criteria:

• Education: M.Sc, B.Pharm, or equivalent degree in a relevant discipline.

• Experience: Hands-on experience in a pharmaceutical QC laboratory compliant with MHRA, WHO, or similar global regulatory bodies.

• Technical Skills: Proficiency in handling analytical instruments (HPLC, GC, UV-Vis, IR, KF, Potentiometer, pH Meter, AAS).

• Documentation: Strong understanding of GDP and pharmaceutical quality systems.

• Preference: Immediate joiners will be given priority.

Benefits of Joining Flamingo Pharmaceuticals Ltd

• Career Growth: Opportunities to build a successful career in a growth-driven organization.

• Regulatory Exposure: Gain expertise in global quality and regulatory environments.

• Competitive Salary: Attractive pay package ranging from INR 3,00,000 to 6,00,000 per annum, depending on role and experience.

• Collaborative Work Culture: Be part of a supportive team focused on excellence in pharmaceutical quality standards.

Walk-In Interview Details

• Dates: 21 & 22 September 2025

• Time: 10:00 AM – 5:00 PM

• Venue: Flamingo Pharmaceuticals Ltd, E28, Opp. Fire Brigade, Near Water Tank, Tondara Village, Taloja MIDC, Panvel – 410208

How to Apply

Candidates can attend the walk-in interview directly at the above venue. Please carry:

• Updated Resume

• Passport-size Photographs

• Educational Certificates

• ID Proof (Aadhaar/PAN)

Can’t attend the walk-in? Send your updated resume to: talojahr@flamingopharma.com

Micro Labs Limited Walk-In Drive in Verna, Goa – September 20, 2025

Are you looking to advance your career in the pharmaceutical industry? Micro Labs Limited, one of India’s fastest-growing pharmaceutical companies, is conducting a Walk-In Interview in Verna, Goa on September 20, 2025. With a strong global presence in more than 60 countries, Micro Labs is a leader in therapeutic segments such as Cardiology, Ophthalmology, Psychiatry, Dermatology, and Diabetology.

This is an excellent opportunity for freshers and experienced professionals to join a company known for innovation, top-ranking brands, and a commitment to quality. Explore career openings across Production, Packing, EHS, Engineering, and IT.

Available Job Roles

1. Production / Packing (B.Pharm / M.Pharm, Freshers or 0–5 years)

• Operate and maintain pharmaceutical production equipment.

• Execute packing operations in compliance with GMP standards.

• Document production activities as per SOPs.

• Work with quality control teams to meet regulatory requirements.

2. Production / Packing FTC (SSC / HSSC / ITI / Diploma)

• Assist in production and packing under supervision.

• Maintain cleanliness and organization of workstations.

• Support inventory and material handling.

• Follow safety protocols and report discrepancies.

3. EHS (BE / Diploma, 5–10 years, ADIS Certified)

• Implement and monitor Environment, Health, and Safety (EHS) policies.

• Conduct risk assessments and ensure regulatory compliance.

• Train staff in workplace safety and emergency procedures.

• Investigate incidents and recommend preventive measures.

4. Engineering (BE / B.Tech / Diploma, 1–5 years)

• Maintain and troubleshoot pharmaceutical manufacturing machinery.

• Plan and execute preventive maintenance schedules.

• Ensure compliance with engineering standards.

• Contribute to process optimization and equipment upgrades.

5. IT (BE / Diploma / BCA, 2–3 years)

• Manage IT infrastructure and systems for smooth operations.

• Provide hardware and software technical support.

• Implement cybersecurity measures.

• Assist in data management and system upgrades.

Candidate Qualifications

• Production / Packing: B.Pharm or M.Pharm for skilled positions; SSC, HSSC, ITI, or Diploma for FTC roles. Freshers or up to 5 years of experience.

• EHS: BE or Diploma with 5–10 years of relevant experience, plus ADIS certification.

• Engineering: BE, B.Tech, or Diploma in Mechanical/Electrical with 1–5 years of experience.

• IT: BE, Diploma, or BCA with 2–3 years of IT experience.

• Male candidates preferred.

• Strong communication skills and knowledge of GMP and safety standards required.

Benefits of Joining Micro Labs Limited

• Competitive salary packages aligned with industry standards.

• Professional growth opportunities in a globally recognized company.

• Collaborative work culture focused on employee well-being.

• Exposure to international operations across 60+ countries.

• Strong emphasis on health, safety, and regulatory compliance.

Walk-In Interview Details

Date: September 20, 2025

Time: 9:30 AM – 1:00 PM

Venue: Micro Labs Limited, Verna, Goa

Documents to Carry:

1. Updated resume

2. Recent passport-size photographs

3. Latest salary slips

4. Aadhaar Card and PAN Card (originals + photocopies)

5. Original mark sheets

Not Able to Attend?

If you cannot attend the walk-in drive, email your updated resume to goahr@microlabs.in or contact 7066039063 for further information.

Project Management R&D Jobs at Unison Pharma

Unison Pharmaceuticals Pvt. Ltd., a leading pharmaceutical company, is urgently hiring Project Management – R&D professionals at its state-of-the-art R&D Centre in Changodar, Ahmedabad. This opportunity is open for freshers and experienced candidates (0–5 years) with BPharm + MPharm/MBA qualifications. Immediate joiners and local candidates from Ahmedabad and nearby areas will be given preference.

Job Details

• Designation: Project Management – R&D

• Company: Unison Pharma

• Qualification: BPharm + MPharm/MBA (Pharmaceutical/Healthcare Management preferred)

• Experience: 0 to 5 years (Freshers eligible)

• Location: Changodar, Ahmedabad

• Job Type: Full-time, Verified Job

Key Responsibilities

1. Assist in managing R&D projects from initiation to completion

2. Coordinate with cross-functional teams to ensure project timelines are met

3. Maintain project documentation and status reports

4. Support project planning, scheduling, and execution

5. Ensure compliance with pharmaceutical industry standards and internal SOPs

Required Skills and Qualifications

• BPharm + MPharm/MBA (Pharmaceutical/Healthcare Management preferred)

• 0 to 5 years of experience in R&D, project management, or pharma operations

• Strong communication and coordination skills

• Ability to work under tight deadlines and deliver results

Benefits

• Salary: ₹3.0 LPA – ₹6.0 LPA

• Transportation facility (bus service) available

• Exposure to innovative pharmaceutical R&D projects

• Growth-oriented work environment with mentorship from experienced professionals

Application Process

Interested and eligible candidates can apply immediately.

Work Location: R&D Centre, Changodar, Ahmedabad

Medical Science Liaison – Oncology

Are you a medical graduate or pharmaceutical science professional passionate about advancing healthcare and oncology research? Johnson & Johnson, a global leader in healthcare innovation, is hiring Medical Science Liaisons (MSLs) – Oncology across Hyderabad, Mumbai, and Chennai.

Key Responsibilities

As an Oncology MSL, you will:

• Serve as the primary scientific liaison for Johnson & Johnson’s Oncology therapy area.

• Map and engage Key Opinion Leaders (KOLs) to establish meaningful scientific collaborations.

• Deliver medical affairs initiatives aligned with franchise and strategic plans.

• Provide scientific training and updates to the sales team.

• Respond to scientific inquiries from healthcare professionals.

• Gather insights from stakeholders to support medical strategy and decision-making.

• Represent the Oncology therapy area in cross-functional internal and external projects.

• Travel extensively (70–80%) to engage stakeholders and support field activities.

Required Qualifications

Education: Medical graduate (MD / MBBS / BDS / MDS) OR

Advanced pharmaceutical degree (PharmD / PhD)

Experience:

0–2 years in pharmaceutical or healthcare industry

Knowledge of medical affairs, regulatory policies, and compliance

Skills:

1. Strong communication and influencing ability

2. Understanding of clinical research and pharma industry code of practice

3. Benefits of Joining Johnson & Johnson

4. Work with a global leader in healthcare innovation.

5. Collaborate with top medical experts and shape oncology strategies in India.

6. Continuous learning with access to the latest scientific advancements.

7. Inclusive, diverse work environment with equal opportunity policies.

8. Competitive compensation and flexible, field-based work arrangements.

Locations

Hyderabad, Mumbai, Chennai

Apothecon Pharmaceuticals Pvt. Ltd. Hiring Trainee, Jr. Officer & Technician

Are you a D. Pharm, B. Pharm, or M. Pharm fresher looking to begin your career in the pharmaceutical industry?

Apothecon Pharmaceuticals Pvt. Ltd., a reputed pharma manufacturing company in Vadodara, Gujarat, is inviting applications from fresh graduates and diploma holders for multiple positions in Production and Quality Systems.

Open Positions

1. Trainee / Jr. Officer (B. Pharm / M. Pharm)

• Assist in granulation, blending, compression, capsule filling, coating, and bottle packing operations.

• Operate advanced equipment such as Glatt Integrated Line, Fette Compression Machine, Auto Coater, Capsule Filling Machines, and Bottle Filling Line.

• Support preparation and execution of SOPs, BMR/BPR documentation, and equipment qualification.

• Ensure compliance with GMP, QMS, and SCADA-based systems.

• Work with senior staff for process improvements and quality checks.

2. Technician (D. Pharm / Diploma in Engineering)

• Operate and clean equipment including Blenders, Sifters, Compression Machines, and Track & Trace Systems.

• Handle SCADA-based machine operations.

• Maintain accurate BMR/BPR records.

• Follow GMP guidelines and ensure smooth plant operations.

Eligibility Criteria

1. Trainee / Jr. Officer: B. Pharm / M. Pharm (Freshers eligible)

2. Technician: D. Pharm / Diploma in Engineering (Freshers eligible)

3. Strong communication and documentation skills.

4. Basic knowledge of GMP and pharmaceutical operations.

Why Join Apothecon Pharmaceuticals Vadodara

• Immediate job opportunities for freshers in the pharma industry.

• Exposure to advanced pharmaceutical machinery and SCADA-based systems.

• Opportunity to learn under experienced industry professionals.

• Long-term career growth in production, quality, and regulatory functions.

How to Apply

Interested candidates should send their updated CV to:

Email: hrd@apotheconpharma.com

Location: Vadodara, Gujarat

Start your career in the pharmaceutical industry with Apothecon Pharmaceuticals Pvt. Ltd., Vadodara.

Medical Coding Freshers in Bangalore – Vee Healthtek 

Walk-in Drive for Medical Coding Freshers in Bangalore – Vee Healthtek | September 20 & 21, 2025

Are you a Life Science graduate eager to start your career in the healthcare industry?

Vee Healthtek Pvt Ltd, a leading name in healthcare technology and services, is conducting a mega walk-in interview for Medical Coding Freshers in Bangalore. With 110 vacancies, this is your chance to enter one of the fastest-growing career fields – Medical Coding.

About Vee Healthtek

Vee Healthtek Pvt Ltd is a trusted healthcare solutions provider specializing in Medical Coding, Revenue Cycle Management, and healthcare support services. With a structured training program, professional work culture, and ample growth opportunities, Vee Healthtek is the ideal place for freshers to build a stable and rewarding career.

Job Opportunity – Medical Coding Fresher

• Position: Medical Coder (Fresher)

• Company: Vee Healthtek Pvt Ltd

• Location: Bangalore (Work from Office)

• Vacancies: 110

• Experience: 0–2 Years

• Salary Package: ₹2 – ₹2.25 LPA (₹21,000/month)

• Shift: Rotational (based on business needs)

• Joining: Immediate

• Job Type: Full-time, Permanent

Eligibility Criteria

Qualification: Only Life Science Graduates (B.Sc, M.Sc, B.Pharm, M.Pharm, Nursing, Biotechnology, Microbiology, Zoology, Botany, Biochemistry, etc.)

Not Eligible: Non-life science degrees, diploma holders, final year students, or candidates with arrears.

Commitment: Minimum 18-month bond. Candidates must submit original 10th & 12th mark sheets at the time of joining.

Interview Schedule & Venue

Dates: September 20 & 21, 2025 (Friday & Saturday)

Reporting Time: Between 9:00 AM – 10:00 AM (No entry after 10:00 AM)

Venue:

Vee Healthtek Pvt Ltd

IndiQube Platina (Shehnai Training Room)

#15, Commissariat Road, Opposite Ashok Nagar Police Station

Near Garuda Mall, Off MG Road, Bengaluru, Karnataka – 560025

Interview Process

1. Technical Assessment

2. Oral Technical Interview

Topics to Prepare:

• Human Anatomy & Physiology

• General Medical Terminologies

• Basics of Medical Coding (ICD & CPT)

Required Documents for Interview

Original 10th & 12th Mark 

Updated Resume

Important Notes

• Only candidates who have completed their graduation and possess original mark sheets will be allowed.

• Entry is restricted to 400 candidates per day on a first-come, first-served basis.

• Commitment of 18 months with original mark sheets submission is mandatory.

Contact Details

Ramesh – HR Department

📞 +91 94432 38706 (Available on WhatsApp)

Don’t miss this opportunity to launch your career in Medical Coding with one of the most reputed organizations in Bangalore.

Oncology Database Analyst Jobs for Freshers at CI Scientists

Work from Home Oncology Database Analyst Jobs for Freshers at CI Scientists

Are you a fresher passionate about oncology research and data analysis? CI Scientists is hiring Oncology Database Analysts to join our Oncology Database Intelligence Team in a work-from-home setup. This is your chance to start a rewarding career in pharmaceutical research, contributing to groundbreaking cancer care projects.

If you hold a Ph.D., M.Pharm, or M.Sc in Life Sciences, Biotechnology, or Pharmaceutical Sciences, we invite you to apply and become part of our innovative oncology research team.

Role: Oncology Database Analyst (Work from Home – Freshers Eligible)

Key Responsibilities:

• Analyze and interpret oncology datasets to generate actionable insights.

• Maintain and enhance our oncology intelligence database.

• Collaborate remotely with cross-functional teams on pharmaceutical research projects.

• Ensure accuracy, compliance, and standardization of oncology data.

• Prepare reports and data visualizations for research communication.

Qualifications:

• Education: Ph.D., M.Pharm, or M.Sc in Life Sciences, Biotechnology, Pharmaceutical Sciences, or related fields.

• Strong interest in oncology and clinical research.

• Analytical mindset; basic knowledge of Excel, Python, or R (preferred but not mandatory).

• Excellent communication and collaboration skills for remote teamwork.

• Freshers welcome – no prior experience required.

Benefits of Joining CI Scientists:

• 100% Work from Home Pharma Job – Flexibility to work anywhere in India.

• Career Growth – Gain hands-on experience in oncology data research.

• Collaborative culture with access to mentorship programs.

• Competitive salary: ₹4,00,000–₹6,00,000 per year.

• Opportunity to contribute to advancing cancer treatment outcomes.

How to Apply:

1. Update your resume with your qualifications and skills.

2. Email your resume to careers@ciscientists.com with the subject line

3. Oncology Database Analyst Application – [Your Name]

4. (Optional) Attach a brief cover letter describing your interest in oncology research.

Deadline: Apply by October 15, 2025 (Applications reviewed on a rolling basis).

Why Choose CI Scientists?

At CI Scientists, you will be part of a team dedicated to pharmaceutical research and oncology innovation. This is the perfect fresher opportunity in pharma research to build a long-term career in oncology database intelligence while working from home.

Life Science Recruiter (US Staffing) 

Learn Power BI for Beginners – Free Certification Access

Are you ready to take the next step in your career with data analytics?

Power BI is one of the most in-demand skills across Pharma, Healthcare, and IT industries. With this tool, you can transform raw data into interactive dashboards and actionable insights that drive smarter decisions.

Why Power BI?

 • Easy-to-use interface with powerful data visualization

 • Widely used in Pharma, Healthcare, and Business Intelligence

 • Enhances your resume with an in-demand skill

 • Opens doors to career growth in data-driven roles

What you’ll get in this course:

• Basics of Power BI and dashboard creation

• Data importing, cleaning, and transformation

• Building reports with real-world examples

• Free certification of completion

Start your journey in data analytics today and stand out in the competitive Pharma & Healthcare job market.

Clinical Publishing Coordinators

Labcorp is hiring Clinical Publishing Coordinators in Bangalore, India. This role is well-suited for life sciences and pharmacy graduates who want to grow their career in clinical research documentation, regulatory publishing, and trial support. The position involves creating and managing investigator manuals, requisitions, and study documents while ensuring compliance with SOPs and timelines.

If you are detail-oriented, committed to quality, and interested in a career in clinical publishing, this is a great opportunity to join a global leader in healthcare and diagnostics.

Key Responsibilities:

• Adhere to departmental SOPs, work instructions, and publishing guidelines.

• Complete mandatory training within given timelines.

• Handle day-to-day publishing tasks with accuracy and efficiency.

• Draft and update investigator manuals, requisitions, and project documents as per scope of work.

• Coordinate translation of project documents to meet deadlines.

• Collaborate with colleagues to deliver precise and complete documentation packages.

• Escalate issues to management as needed.

• Take on additional responsibilities as assigned.

Qualifications:

• Bachelor’s degree in Life Sciences, Pharmacy, Biotechnology, or related field.

• Prior experience in clinical publishing, research, or regulatory documentation is an advantage.

• Excellent attention to detail and time management skills.

• Proficiency in MS Office and familiarity with document management systems is desirable.

Why Join Labcorp?

• Be part of a leading global CRO and healthcare company.

• Inclusive and diverse work environment with equal opportunity for all.

• Continuous training and exposure to international projects for professional growth.

• Competitive salary with attractive benefits.

Clinical Research Coordinators

CliniMed Lifesciences is looking for Clinical Research Coordinators in Kolkata. This is a full-time, on-site opportunity ideal for fresh graduates (BSc, MSc, or B.Pharm) who want to build a career in the rapidly growing field of clinical research. If you are interested in clinical trials, regulatory compliance, and quality-driven work, this could be the right start for you.

Key Responsibilities:

• Process incoming batches on time while ensuring accuracy and quality.

• Maintain complete and transparent audit trails for all activities.

• Support the team with on-call or after-hours duties when required.

• Stay updated with relevant SOPs and strictly follow company policies.

• Work with colleagues to keep the workspace organized and compliant with SOPs.

• Complete required training and keep training records current.

• Accurately document activities and results for quality checks and reference.

• Contribute ideas for process improvements and support implementation.

Requirements:

• Bachelor’s degree in Life Sciences or related field.

• 0–2 years of lab experience, preferably in sample handling and processing.

• Strong organizational and communication skills.

• Ability to work both independently and in a team.

• High attention to detail and commitment to quality.

• Basic knowledge of lab equipment and software.

• Flexibility to manage shifting priorities in a fast-paced environment.

Benefits:

• Competitive salary with benefits.

• Work with a reputed healthcare company.

• Friendly and collaborative work culture.

• Clear pathways for career growth and skill development.

• Rewards and recognition for excellent performance.

About Us:

Labcorp is a global healthcare leader offering diagnostic and clinical research testing solutions. Our focus is on accuracy, innovation, and delivering exceptional results to clients worldwide.

Our Values:

• Promoting diversity, equality, and inclusion in the workplace.

• Respecting individual perspectives and differences.

• Upholding quality and accuracy in every process.

• Encouraging open communication and teamwork.

Equal Opportunity:

Labcorp is an Equal Opportunity Employer. We welcome applicants from all backgrounds and are committed to building a respectful, inclusive, and discrimination-free environment.

Six Sigma White Belt Certification

What is Six Sigma?

Six Sigma is a globally recognized methodology for process improvement, quality management, and operational excellence. It uses data-driven techniques and structured problem-solving to eliminate errors, reduce variation, and deliver consistent, high-quality outcomes.

Today, Six Sigma is applied across industries—pharmaceuticals, healthcare, IT, manufacturing, finance, and services—to improve efficiency, cut costs, and drive business growth.

Why Six Sigma White Belt?

The White Belt Certification is the entry point into the Six Sigma journey. It introduces you to the core principles, concepts, and tools of Six Sigma, making it ideal for:

• Students seeking to strengthen their resumes

• Professionals looking to upskill and stand out

• Organizations encouraging a culture of continuous improvement

By completing your White Belt, you’ll gain:

• A strong foundation in Six Sigma methodology

• Understanding of DMAIC (Define, Measure, Analyze, Improve, Control)

• Awareness of how Six Sigma applies to real-world processes

• A globally recognized credential to boost your career

Who Should Enroll?

• Students preparing for placements

• Freshers entering corporate jobs

• Working professionals in pharma, IT, healthcare, finance, and consulting

• Anyone curious about process excellence and quality management

• No prior experience is required.

Certification Process

We act as a trusted mediator, connecting learners with the Council for Six Sigma and Six Sigma Online.

Benefits of Six Sigma White Belt Certification

• Enhance your career prospects with a recognized certification

• Gain access to higher-level Six Sigma belts (Yellow, Green, Black)

• Stand out in job applications, especially in pharma, research, and corporate roles

• Build a global professional profile

Sample Handling Assistant at labcorp

Are you a detail-oriented individual with excellent organizational skills? Do you have a passion for quality and accuracy in a laboratory setting? We are seeking a highly motivated and skilled Sample Handling Assistant I to join our team. This is a full-time position that requires strong attention to detail, excellent communication skills, and a commitment to delivering high-quality results.

Responsibilities:

• Ensure received batches are timely processed with the highest level of quality and accuracy.

• Generate an appropriate audit trail of all activities to maintain transparency and accountability.

• Perform on-call and after-hours duties as needed to support the team and maintain operational continuity.

• Ensure timely reading of concerned Standard Operating Procedures (SOPs) and adherence to all company policies and procedures.

• Work collaboratively with the team to maintain a clean and organized workspace, adhering to departmental and interdepartmental SOPs.

• Perform all required training and maintain an up-to-date training file.

• Document all activities and results properly for future reference and quality control.

• Collaborate with the team to generate new ideas for process improvement and implement changes as needed.

Requirements:

1. Bachelor’s degree in a life science or related field.

2. 0-2 years of experience in a laboratory setting, with a focus on sample handling and processing.

3. Excellent communication and organizational skills.

4. Ability to work independently and as part of a team.

5. Strong attention to detail and commitment to quality.

6. Familiarity with laboratory equipment and software.

7. Ability to work in a fast-paced environment with changing priorities.

Benefits:

• Competitive salary and benefits package.

• Opportunity to work with a leading healthcare company.

• Collaborative and dynamic work environment.

• Opportunities for professional growth and development.

• Recognition and rewards for outstanding performance.

About Us:

Labcorp is a leading global healthcare company that provides comprehensive diagnostic and clinical research testing services. We are committed to delivering high-quality results and exceptional customer service.

Our Values:

• Diversity and inclusion in the workforce and a commitment to equality and non-discrimination.

• Respect for individual differences and perspectives.

• Strong commitment to quality and accuracy in all our work.

• Open communication and collaboration with colleagues and external partners.

Equal Employment Opportunity:

Labcorp is an Equal Opportunity Employer and welcomes applications from diverse candidates. We recognize the value of diversity and inclusion in our workforce and are committed to creating a work environment that is free from harassment and discrimination.

Medical Information Specialist (MIS)

About ProPharma

For the past two decades, ProPharma has been supporting the health and well-being of patients by providing expert guidance to biotech, medical device, and pharmaceutical companies of all sizes. Our goal is to help clients confidently advance scientific innovations and bring new therapies to market. ProPharma works closely with clients through an advise-build-operate approach throughout the entire product lifecycle. With deep expertise in regulatory sciences, clinical research, quality and compliance, pharmacovigilance, medical information, and R&D technology, we provide fully customizable consulting solutions that reduce risk and accelerate high-profile drug and device programs.

Medical Information Specialist (MIS)

The MIS role is part of ProPharma’s Medical Information Contact Center. It ensures adherence to regulations, industry standards, and internal/client policies when providing medical information and documenting adverse events, special situations, and product complaints.

Key Responsibilities

• Medical Information Services:

• Respond to unsolicited inquiries from healthcare professionals, consumers, and other external stakeholders via phone, email, website, fax, letters, and scientific meetings.

• Provide accurate medical and safety information, both labeled and unlabeled, following regulatory guidelines, industry standards, and internal/client procedures.

• Identify, document, and report adverse events, pregnancy cases, special situations, and product complaints clearly and accurately, in line with SOPs and client requirements.

• Ensure all tasks are completed within agreed deadlines.

• Formulate responses using approved labeling, company standard responses, and scientific literature; assist in drafting custom responses when needed.

• Log all inquiries accurately and promptly into the Inquiry Handling System.

General Duties:

• Provide after-hours support on a rotational basis as required.

• Follow company and country-specific privacy and confidentiality policies.

• Adhere to health and safety guidelines.

• Undertake additional tasks as assigned by the Manager.

Qualifications & Skills:

• Degree in Life Sciences, Nursing (RN/BS/BA/MS), or Pharmacy.

• Strong verbal and written communication skills, professional phone etiquette, and empathetic customer service.

• Fluent, grammatically correct writing in English.

• Knowledge of medical terminology, pathophysiology, pharmacology, regulations, and industry standards.

• Strong analytical, critical thinking, and problem-solving skills.

• Ability to multitask, prioritize, and work under time constraints with attention to detail.

• Self-motivated and proactive; able to work independently and as part of a team.

• Willingness to take on additional projects and responsibility.

• Proficient in Microsoft Office, Adobe Acrobat, and document management systems; quick to learn other platforms, including inquiry handling databases.

Our Commitment:

At ProPharma, we value diversity, equity, and inclusion, creating a workplace where every employee can be their authentic self. We encourage innovation, collaboration, and entrepreneurial thinking, providing a safe and supportive environment for everyone to succeed.

Note: ProPharma Group does not accept unsolicited resumes from recruiters or third parties. Please refrain from making phone calls or sending emails regarding this posting.

Omega Healthcare is hiring Non-certified Medical coders

Omega Healthcare is a leading global healthcare BPO specializing in revenue cycle management, medical coding, and healthcare analytics. With a strong presence in Chennai, Omega is known for its employee-friendly policies, structured training programs, and career growth opportunities.

Detailed Job Description

 Job Role: Medical Coder (Trainee to Full-Time)

Omega Healthcare is offering a unique opportunity for freshers and non-certified candidates to enter the lucrative field of medical coding with free certification training.

Trainee Medical Coder (IPDRG, ED, EM, EM Surgery, HH)

Key Highlights:

1. Free Training: 5-month IPDRG & CCS certification (no cost).

2. No Bond: No mandatory service agreement.

3. Job Guarantee: 100% placement at Omega post-training.

4. Salary Growth: Starting at ₹22 000 CTC (₹18,000 take-home) with ₹5,000 increments every 6 months.

5. Performance Incentives: Monthly rewards based on productivity.

6. Work Location: Chennai (Work from Office).

7. Fixed Weekends Off: Saturday & Sunday holidays.

Eligibility Criteria

Who Can Apply?

• Paramedical Graduates:

1. B.Pharma, M.Pharma, Pharm.D, D.Pharma

2. B.Sc Nursing, PB B.Sc Nursing, GNM

3. B.Sc Operation Theatre Technology, Anesthesia, Optometry

4. B.Sc Perfusion Tech, Cardiac Care, Radiology

• Life Science Graduates (Microbiology, Biotechnology, Biochemistry, etc.)

• Freshers Welcome! (No prior coding certification required)

Benefits of Joining Omega Healthcare

• Zero-cost certification (IPDRG & CCS – valued at ₹50,000+).

• Stable career path in healthcare BPO.

• Rapid salary growth with assured increments.

• Performance-based incentives (extra earnings).

• Fixed weekends off for work-life balance.

Location: Bangalore

Shift: 9:00 AM – 6:00 PM (Mon-Fri)

Hiring Freshers for Medical Scribing in Value Health

Value Health Inc, a fast-growing life sciences consulting and digital transformation company, is hiring Medical Scribes in Coimbatore, Tamil Nadu. This full-time, on-site role in the US healthcare domain is ideal for graduates in healthcare, life sciences, or related fields who want to build a career in medical documentation and scribing.

As a Medical Scribe, you will play a crucial role in assisting US-based physicians by documenting patient reports, reducing delays in care, and improving overall efficiency in the healthcare system.

Key Responsibilities

• Assist US-based physicians with real-time medical documentation

• Prepare and finalize reports for patient exams

• Verify patient data and exam details for accuracy

• Reduce physician workload by handling non-clinical documentation

• Support timely patient care while minimizing physician burnout

• Maintain knowledge of medical and radiology terminology

Qualifications

1. Graduate in Healthcare, Life Sciences, or related field (preferred)

2. Experience: 0–5 years (freshers welcome)

3. Prior experience in Medical Scribing, Medical Transcription, Billing, or Coding is a plus

4. Strong communication skills for interacting with physicians in real-time

5. Active listening skills to document physician instructions accurately

6. Open to night and day shifts

7. Familiarity with radiology terminology is an added advantage

Why Join Value Health Inc?

• Dynamic Growth Environment – Work with a rapidly expanding company serving Fortune 500 clients

• Continuous Learning Hub – Access to training and professional development opportunities

• Impactful Role – Directly contribute to improving patient care and reducing physician burnout

• Innovation-driven Culture – Encourages creative problem-solving and independent thinking

Job Details

• Job Title: Medical Scribing (US Shift)

• Location: Coimbatore, Tamil Nadu, India (On-site)

• Employment Type: Full-time

• Experience Required: 0–5 years

• Salary Range: ₹2,20,000 – ₹3,80,000 per annum (INR)

Regulatory Toxicology Internship

Are you a postgraduate in Life Sciences, Pharma, Toxicology, or Chemistry eager to explore the world of chemical safety and regulatory compliance? Here’s your golden opportunity!

Freyr, a leading global regulatory solutions company, is inviting applications for its Regulatory Toxicology (CSRA) Internship in Hyderabad. This 8-month structured internship offers hands-on exposure to international guidelines (OECD, ICH) and real-world experience in consumer product safety, cosmetics, chemicals, and biocides.

If you’re passionate about regulatory science and want to build a career in toxicology, compliance, or product safety, this role is tailored for you.

Internship Details

• Position: Intern – Regulatory Toxicology (CSRA)

• Job ID: JOB_3992

• Location: Hyderabad, Telangana – Intern Office

• Duration: 8 months (240 days)

• Mode: Office-based Internship

• Hiring Organization: Freyr Solutions

• Stipend Range: ₹15,000 – ₹25,000 per month (approx.)

Key Responsibilities

As an intern, you will:

1. Conduct literature reviews and scientific writing on toxicological safety.

2. Support regulatory compliance activities for chemicals, cosmetics, and biocides.

3. Gain exposure to global frameworks (OECD, ICH, REACH, US/EU regulations).

4. Assist in preparing technical documentation, safety reports, and CSRA dossiers.

5. Work closely with experts to learn about consumer product safety strategy.

Required Qualifications

• Fresh postgraduates in Life Sciences, Pharmacology, Toxicology, Regulatory Affairs, or Chemistry.

• Strong interest in chemical safety, product compliance, and toxicology.

• Skills in Excel, PowerPoint, scientific documentation, and technical writing.

• Understanding of global regulatory guidelines (OECD, ICH preferred).

• Detail-oriented, curious, and self-driven to learn.

Internship Benefits

• Real-time training in global regulatory toxicology.

• Direct mentorship from regulatory science professionals.

• Exposure to international compliance systems.

• Opportunity to build a career in toxicology, regulatory affairs, and product safety.

 Send your CV with subject line “Intern – Regulatory Toxicology (JOB_3992)” :

Assistant Data Manager on a Clinical Research Project 

Tata Memorial Centre (TMC), Mumbai, a Grant-In-Aid Institute of the Department of Atomic Energy, Government of India, has announced recruitment for the position of Assistant Data Manager on a Clinical Research Project (No.3424).

This is an excellent opportunity for postgraduates in Science/Commerce with computer training to contribute to one of India’s premier cancer research institutes.

Job Details

• Organization: Tata Memorial Hospital (Tata Memorial Centre)

• Position: Assistant Data Manager

• Location: Mumbai, Maharashtra

• Vacancies: 01

• Employment Type: Contract (Initially for 6 months)

• Salary: ₹27,000/- per month

• Last Date to Apply: 10th September 2025, 5:30 PM (IST)

• Application Mode: Online

Key Responsibilities

1. Assist in clinical research data management for investigator-initiated trials.

2. Maintain accurate databases, records, and documentation.

3. Support in data entry, validation, and reporting for research projects.

4. Collaborate with research staff and ensure compliance with hospital protocols.

Qualifications & Experience

• Education: Post Graduate Degree in Science/Commerce with a 6-month computer course from a recognized institute or MS-CIT certificate.

• Experience: 1–2 years in data management at Tata Memorial Hospital is desirable.

• Fresher candidates can also apply (must fill experience as “Fresher”).

Benefits

• Fixed monthly remuneration of ₹27,000/-.

• Opportunity to gain hands-on experience in clinical research and data management at a reputed institute.

• Exposure to investigator-led projects in healthcare and oncology research.

Application Process

• Apply online through the official TMC portal: Click Here (Ref. No. TMC/AD/111/2025)

• Last date to submit application: 10th September 2025 (5:30 PM IST)

• Shortlisted candidates will be notified via email for interview/test.

• Carry original documents & one set of copies during the interview.

Scientific Writing in Health Research

About the Course

The ICMR – National Institute of Epidemiology (NIE), one of India’s premier research institutions under the Indian Council of Medical Research (ICMR), offers a high-impact online certification program titled:

NleCer 103: Scientific Writing in Health Research

This course is designed to strengthen the ability of healthcare professionals, researchers, and academicians in scientific writing, research communication, and publication ethics. It equips participants with the skills to present their research work effectively in peer-reviewed journals, improve the clarity and impact of manuscripts, and enhance overall research communication standards.

Key Highlights

• Offered by ICMR–NIE, a Government of India institute with national and global recognition.

• Structured and delivered by leading scientists and research experts.

• Comprehensive coverage of scientific writing in health and biomedical research.

• Recognized and valued certification, beneficial for academic progression, research careers, and industry roles.

• Accessible online through SWAYAM platform.

What You Will Learn

1. By the end of the course, participants will gain a strong foundation in:

2. Principles of scientific writing and effective communication

3. Manuscript preparation and journal submission process

4. Understanding publication ethics and avoiding plagiarism

5. Writing abstracts, research papers, and reports with clarity

6. Improving overall quality and acceptance rate of research publications

Why You Should Join

In today’s competitive research and academic environment, the ability to communicate science effectively is as important as conducting high-quality research. This certification adds credibility to your professional profile and gives you an edge in academic, clinical, and pharmaceutical careers.

Many faculty members, researchers, and students across India, including principals of pharmacy colleges and senior academicians, have already benefited from this program and proudly showcase their achievement.

Certification

On successful completion, participants receive a nationally recognized e-certificate from ICMR–NIE. The certificate highlights the participant’s performance (with score) and is jointly signed by senior scientists and directors of ICMR–NIE.

Who Can Apply?

• Undergraduate and postgraduate medical, pharmacy, nursing, and life sciences students

• Research scholars and Ph.D. candidates

• Faculty members and academicians

• Industry professionals in healthcare, clinical research, and pharmaceuticals

Duration & Mode

• Mode: 100% Online (via SWAYAM platform)

• Duration: Self-paced within the enrollment period

• Examination: Online assessment with graded certification