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
Frequently Asked Questions
Q1. What is the role of a Pharmacovigilance Operations Associate at Amgen?
Ans: This role involves supporting drug safety activities such as literature surveillance, safety data review, ICSR identification, signal detection support, and regulatory compliance processes.
Q2. Who can apply for this Amgen Pharmacovigilance job?
Ans: Candidates with qualifications such as B.Pharm, M.Pharm, Pharm.D, B.Sc/M.Sc Life Sciences, Biotechnology, Microbiology, Biochemistry, Clinical Research, Biomedical Sciences, Nursing, Medicine, or related healthcare disciplines can apply.
Q3. What is the required experience for this position?
Ans: Amgen is looking for candidates with around 1–3 years of experience in pharmacovigilance, drug safety, clinical research, literature review, regulatory compliance, or related life sciences fields.
Q4. Is this a work-from-home opportunity?
Ans: No. This position is an on-site full-time role based in Hyderabad, Telangana
Q5. What databases are useful for this Pharmacovigilance role?
Ans: Experience with scientific databases such as Embase, Medline, and BIOSIS is preferred for literature surveillance activities.
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