Thermo Fisher Scientific is currently hiring for two exciting healthcare and life sciences positions in India โ Program Documentation Specialist I and Pharmacovigilance Physician. These opportunities are ideal for professionals in pharmacovigilance, clinical research, medical documentation, regulatory affairs, and healthcare domains looking to work with a globally recognized CRO and scientific organization.
The company is offering hybrid and fully remote opportunities in Bangalore and Hyderabad respectively. Candidates with experience in clinical documentation, safety reporting, medical review, regulatory submissions, and pharmacovigilance are encouraged to apply.
1. Program Documentation Specialist I โ Bangalore
Job Overview
Thermo Fisher Scientific is seeking a Program Documentation Specialist I to support program managers in handling document preparation, quality compliance, change orders, and electronic documentation systems. The role focuses heavily on document control, quality systems, and regulatory compliance within scientific and healthcare programs.
Job Details
- Role: Program Documentation Specialist I
- Location: Bangalore, India
- Job Type: Full-Time
- Work Mode: Hybrid
- Experience Required: 2โ3 Years
- Application Deadline: May 28, 2026
Key Responsibilities
- Prepare and submit documentation through OCPLM PPM change orders.
- Ensure document consistency and compliance with SOPs.
- Manage document uploads, approvals, and linking processes.
- Track and communicate change order status updates.
- Maintain organized electronic Design and Development Files (eDDFs).
- Support ISO standard compliance and quality documentation procedures.
Required Qualifications
- Bachelorโs degree from a recognized university.
- 2โ3 years of industrial or documentation experience.
- Experience with Oracle PLM, Documentum, or change control systems.
- Strong knowledge of Microsoft Office 365 and Agile systems.
- Experience with Power BI dashboards and reporting.
- Excellent communication and organizational skills.
Preferred Skills
- Clinical documentation experience for regulatory submissions.
- Exposure to 510k, PMA, IVDR, PMDA, or NMPA documentation.
- Knowledge of instruments, software, consumables, and reagent documentation.
Since the role is related to documentation control, quality systems, clinical/regulatory documentation, and scientific programs, the most relevant degrees would be:
- B.Pharm
- M.Pharm
- Pharm.D
- BSc Life Sciences
- MSc Life Sciences
- Biotechnology
- Microbiology
- Biochemistry
- Biomedical Sciences
- BTech Biotechnology
- BTech Biomedical Engineering
- B.E/B.Tech (relevant scientific or healthcare streams)
- Life Science-related graduates
Candidates with experience in:
- Documentation management
- Regulatory affairs
- Clinical documentation
- Quality assurance
- PLM/Documentum systems
- Medical device documentation
2. Pharmacovigilance Physician โ Remote
Job Overview
Thermo Fisher Scientific is also hiring a Pharmacovigilance Physician for its global pharmacovigilance operations. This fully remote role involves medical review of adverse events, safety signal detection, aggregate reporting, benefit-risk evaluation, and regulatory safety compliance.
This is an excellent opportunity for MBBS and MD professionals interested in drug safety and clinical research careers.
Job Details
- Role: Pharmacovigilance Physician
- Location: Hyderabad, India
- Work Mode: Fully Remote
- Shift: Night Shift
- Experience Required: Clinical or Pharmacovigilance experience preferred
- Employment Type: Full-Time
Key Responsibilities
- Perform medical review of adverse event cases and safety reports.
- Assess seriousness, expectedness, and causality of ICSRs.
- Review PSUR, PBRER, DSUR, RMP, REMS, and CSR safety content.
- Conduct signal detection and benefit-risk analysis.
- Provide pharmacovigilance consultation to sponsors and project teams.
- Support regulatory safety submissions and labeling activities.
Eligibility Criteria
Educational Qualification
- MD or equivalent degree preferred
OR - MBBS with 2 years of clinical experience
Required Skills
- Strong pharmacology and clinical knowledge.
- Understanding of FDA, EMA, ICH, and GCP guidelines.
- Experience with MedDRA, safety databases, and clinical trial safety.
- Excellent communication and analytical skills.
- Ability to work independently in global teams.
Why Join Thermo Fisher Scientific?
Working at Thermo Fisher Scientific offers professionals the opportunity to contribute to global healthcare innovation and clinical research.
Employee Benefits
- Global career growth opportunities
- Exposure to international clinical trials
- Remote and hybrid work flexibility
- Collaborative scientific environment
- Training and development programs
- Work with top pharmaceutical and biotech companies
How to Apply
Application Link For Program Documentation Specialist I
Application Link For Pharmacovigilance Physician
