Amgen Hiring Sr. Associate Pharmacovigilance Operations
- Opportunity in Pharmacovigilance at Amgen, Hyderabad
- About Amgen India
- Role Overview: Sr. Associate – Pharmacovigilance Operations
- Job Location
- Educational Qualifications
- Experience Required
- Key Responsibilities
- Required Skills and Competencies
- Pharmacovigilance Expertise
- Collaboration & Documentation
- Compliance & Reporting
- Bonus Skill
- How to Apply?
- Job Snapshot Table
Amgen Hiring Sr. Associate – Pharmacovigilance Operations | B.Pharm / M.Pharm / Life Sciences | 5-9 Years | Hyderabad Location
Apply for Sr. Associate Pharmacovigilance Operations at Amgen in Hyderabad. Candidates with B.Pharm/M.Pharm/Life Sciences and 5-9 years of experience in PASR writing are eligible.
Opportunity in Pharmacovigilance at Amgen, Hyderabad
Amgen, a global biopharmaceutical leader, is actively seeking a Sr. Associate – Pharmacovigilance Operations to join its Hyderabad team. This role is ideal for professionals with strong experience in pharmacovigilance report writing and a passion for global regulatory compliance.
About Amgen India
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📱 Join Click HereAmgen is renowned worldwide for its cutting-edge research and biopharmaceutical innovation. The Hyderabad location supports global operations in safety, regulatory, and R&D functions, providing a collaborative and impactful work environment.
Role Overview: Sr. Associate – Pharmacovigilance Operations
Job Location
- Hyderabad, Telangana, India
- On-site Role
Educational Qualifications
- Bachelor’s or Master’s degree in Life Sciences or Pharmacy
Experience Required
- Total experience: 5–9 years
- Minimum 2–3 years in Periodic Aggregate Safety Report (PASR) writing
Key Responsibilities
- Compile and author various PASRs including DSUR, PBRER/PSUR, SSUR, PADER, and country-specific reports (e.g., Korea PSUR, Brazil PSUR)
- Collaborate with cross-functional stakeholders for data gathering
- Coordinate report timelines and ensure regulatory compliance
- Conduct peer review/quality control of safety content
- Archive and manage documentation workflows
- Distribute final reports to CROs and global partners
- Generate and monitor safety KPIs and compliance metrics
Required Skills and Competencies
Pharmacovigilance Expertise
- Knowledge of global safety report types (DSUR, PSUR, PADER, etc.)
- Familiarity with regulatory guidelines and medical writing standards
Collaboration & Documentation
- Strong cross-functional coordination
- Peer QC and stakeholder comment resolution
Compliance & Reporting
- Ensure all safety documents meet regulatory timelines and formats
- Maintain awareness of evolving pharmacovigilance and regulatory landscapes
Bonus Skill
- Literature management involvement is a plus
How to Apply?
Interested and qualified candidates may apply directly via the official Amgen careers portal: Apply Now
Job Snapshot Table
| Company Name | Current Vacancies | Required Education | Experience Required |
|---|---|---|---|
| Amgen | Sr. Associate – Pharmacovigilance | B.Pharm / M.Pharm / Life Sciences | 5–9 Years |
Amgen is hiring Sr. Associate Pharmacovigilance Operations in Hyderabad for professionals with 5–9 years of experience in PASR writing. Apply now!
To apply for this job please visit amgen.wd1.myworkdayjobs.com.
