Thermo Fisher Scientific Hiring Program Documentation Specialist & Pharmacovigilance Physician
Thermo Fisher Scientific is hiring for Program Documentation Specialist I and Pharmacovigilance Physician roles in India.
These opportunities are ideal for candidates interested in Medical Documentation, Regulatory Affairs, Pharmacovigilance, Drug Safety, Clinical Research, Safety Reporting, and Healthcare Compliance careers.
📋 Thermo Fisher Scientific Hiring Overview
- Company: Thermo Fisher Scientific
- Locations: Bangalore & Hyderabad
- Work Mode: Hybrid & Fully Remote
- Industry: Clinical Research / Healthcare / Pharmacovigilance
- Job Type: Full-Time
🏢 About Thermo Fisher Scientific
Thermo Fisher Scientific is one of the world’s leading scientific and healthcare organizations supporting pharmaceutical, biotechnology, clinical research, and healthcare innovation globally.
The company offers opportunities in Pharmacovigilance, Clinical Research, Regulatory Affairs, Medical Documentation, and Global Healthcare Compliance projects.
📄 Program Documentation Specialist I – Bangalore
🎓 Qualification
- B.Pharm / M.Pharm / Pharm.D
- BSc / MSc Life Sciences
- Biotechnology / Microbiology / Biochemistry
- Biomedical Sciences
- BTech Biotechnology / Biomedical Engineering
- Relevant Scientific or Healthcare Degrees
🧑💻 Experience Required
- 2–3 Years
📌 Key Responsibilities
- Prepare and manage documentation through change orders
- Maintain document consistency and SOP compliance
- Manage electronic Design & Development Files (eDDFs)
- Track documentation approvals and updates
- Support ISO compliance and quality systems
- Maintain organized regulatory documentation workflows
⭐ Required Skills
- Oracle PLM / Documentum knowledge
- Documentation management experience
- Quality systems & regulatory compliance understanding
- Power BI and Microsoft Office proficiency
- Strong communication and coordination skills
💊 Pharmacovigilance Physician – Remote
🎓 Qualification
- MD Preferred
- MBBS with 2 Years Clinical Experience
🧑💻 Experience Required
- Clinical or Pharmacovigilance Experience Preferred
- Night Shift Role
📌 Key Responsibilities
- Perform medical review of adverse event cases
- Assess seriousness, expectedness, and causality
- Review PSUR, DSUR, PBRER, RMP, REMS & CSR reports
- Conduct signal detection and benefit-risk analysis
- Support global regulatory safety submissions
- Provide pharmacovigilance consultation to sponsors
⭐ Required Skills
- Strong pharmacology and clinical knowledge
- FDA, EMA, ICH & GCP guidelines understanding
- Safety database & MedDRA knowledge
- Clinical trial safety experience
- Excellent analytical and communication skills
🌍 Benefits of Working at Thermo Fisher Scientific
- Global healthcare and scientific exposure
- Remote and hybrid work flexibility
- Career growth in Pharmacovigilance & Regulatory Affairs
- Collaborative scientific work culture
- Training and development programs
- Opportunities with top pharma and biotech clients
📄 Resume & Interview Tips
- Highlight documentation, PV, or clinical experience clearly
- Mention safety reporting and regulatory compliance knowledge
- Add Oracle PLM, MedDRA, or PV database exposure if available
- Showcase communication and analytical abilities
- Keep resume ATS-friendly and concise
🚀 Job Application Links
Please make sure to read the complete job description carefully before submitting your application. Make sure your Pharmacovigilance, Clinical, Regulatory, or Documentation experience aligns with the selected role before proceeding.
