Apotex is hiring for the position of Senior Analyst, Drug Information & Risk Management in Mumbai, Maharashtra. The role involves responding to medical inquiries, preparing and updating risk management documents, conducting medical literature research, and supporting the safe and effective use of Apotex pharmaceutical products.
Candidates with 1–3 years of experience in Pharmacovigilance and a relevant pharmacy, science, or healthcare qualification can review the job requirements below.
Job Details
| Particulars | Details |
|---|---|
| Company | Apotex Inc. |
| Job Title | Senior Analyst, Drug Information & Risk Management |
| Job Location | Mumbai, Maharashtra, India – 400079 |
| Experience | 1–3 years in Pharmacovigilance |
| Job Function | Drug Information & Risk Management |
| Job Posting Date | October 22, 2026 |
About Apotex Inc.
Apotex is a Canadian-based global health company focused on improving access to affordable, innovative medicines and health products. Its portfolio includes generic, biosimilar, innovative branded pharmaceuticals, and consumer health products. Headquartered in Toronto, the company operates globally, including in India, the United States, and Mexico.
Key Responsibilities
The selected candidate will be responsible for:
- Responding to medical inquiries from healthcare professionals, sales representatives, and internal customers through written and verbal communication.
- Evaluating and analyzing medical inquiries to provide accurate, balanced, and timely responses.
- Coordinating the preparation and updating of global Risk Management Plans and Risk Evaluation and Mitigation Strategies documents.
- Researching and interpreting medical and scientific information.
- Creating and peer-reviewing medical information documents, including response documents, recall Q&As, and bulletins.
- Ensuring compliance with standard operating procedures for adverse event and quality complaint reporting.
- Maintaining product databases, files, and medical information records.
- Supporting departmental and cross-functional projects and preparing reports.
- Keeping up to date with therapeutic developments and medical information regulations.
- Providing scheduled on-call coverage and after-hours support for the DISPedia unit.
- Following applicable regulatory, quality, safety, environmental, and business compliance policies.
Eligibility and Qualifications
Candidates should have one of the following qualifications listed in the job description:
- Bachelor of Pharmacy (B.Pharm)
- B.Sc. or a diploma in a health- or science-related discipline
- Master of Pharmacy (M.Pharm)
- Bachelor of Dental Surgery (BDS)
Experience requirement: 1–3 years of experience in Pharmacovigilance.
Required Skills and Knowledge
Applicants should have the following skills and knowledge:
- Excellent written and oral communication skills.
- Proficiency in Microsoft Office applications, including Excel, PowerPoint, Word, and Outlook.
- Knowledge of the ArisG Safety Database, MedDRA, and Argus.
- Familiarity with Embase and MLM databases.
- Knowledge of online medical literature searching and review.
- Technical and scientific skills in researching and interpreting medical information.
