This role is suitable for professionals with experience in pharmacovigilance, literature screening, safety review, and Individual Case Safety Report (ICSR) identification.
Job Overview
| Particulars | Details |
|---|---|
| Position | Pharmacovigilance Operations Associate |
| Company | Amgen |
| Location | Hyderabad, Telangana |
| Job Type | Full-Time |
| Experience | 1 - 3 years |
| Category / Department | Pharma |
| Application Mode | Online |
🏢 About Amgen
Amgen is a global biotechnology organization focused on developing innovative therapies to address serious health conditions.
The company combines advanced science, research capabilities, and biotechnology expertise to create medicines that improve patient outcomes worldwide.
serious health conditions
📝 Job Description
🚀 Amgen Hiring | Pharmacovigilance Operations Associate | Drug Safety Jobs
🏢 Company: Amgen
💼 Position: Pharmacovigilance Operations Associate
📍 Location: Hyderabad, Telangana
🏢 Work Mode: On-Site
📄 Employment Type: Full-Time
📈 Experience: 1–3 Years
🏭 Industry: Biotechnology | Pharmacovigilance | Drug Safety
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🎓 Eligible Qualifications
✔ B.Pharm
✔ M.Pharm
✔ Pharm.D
✔ B.Sc / M.Sc Life Sciences
✔ Biotechnology
✔ Microbiology
✔ Biochemistry
✔ Clinical Research
✔ Biomedical Sciences
✔ Nursing
✔ Medicine
✔ Allied Healthcare Disciplines
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⭐ Preferred Experience
Candidates with experience in:
✔ Drug Safety Operations
✔ Literature Surveillance
✔ Clinical Research
✔ Regulatory Compliance
✔ Safety Database Systems
✔ Healthcare or Life Sciences Projects
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🌟 Why Join Amgen?
✨ Opportunity to work with a leading biotechnology company
✨ Exposure to global pharmacovigilance operations
✨ Career growth in drug safety and regulatory sciences
✨ Work with advanced healthcare technologies
✨ Collaborative research environment
✨ Professional learning opportunities
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Interested candidates can apply through the official Amgen career portal.
Job ID: R-248109
🎯 Key Responsibilities
- ✓ Perform literature surveillance activities using scientific databases.
- ✓ Review publications to identify potential safety information.
- ✓ Evaluate literature articles for ICSR criteria.
- ✓ Support signal detection and periodic safety reporting activities.
- ✓ Review safety-related scientific information and coordinate follow-up actions.
- ✓ Request and manage full-text articles when required.
- ✓ Collaborate with safety teams and internal stakeholders.
- ✓ Support pharmacovigilance audits and regulatory requirements.
💡 Required Qualifications & Skills
- ✓ Pharmacovigilance process knowledge
- ✓ Literature screening and review experience
- ✓ Understanding of drug safety regulations
- ✓ ICSR identification knowledge
- ✓ Experience with databases like Embase, Medline, BIOSIS
- ✓ Good analytical and communication skills
- ✓ Strong attention to detail
- ✓ Time management and prioritization skills
- ✓ Knowledge of safety reporting processes