Pharmacovigilance Hiring – Apotex Senior Analyst – Drug Information & Risk Management

Apotex is hiring a Senior Analyst – Drug Information & Risk Management in Mumbai, Maharashtra to support its multidisciplinary healthcare team.
The role focuses on providing professional, unbiased, clinically relevant, and timely medical information regarding Apotex products to internal and external customers.
The position also involves Risk Management Plans, medical inquiry responses, medical literature research, safety information, medical documentation, and pharmacovigilance compliance.
Candidates with B.Pharm, M.Pharm, B.Sc., BDS, or a Diploma in Health/Science-related discipline and 1–3 years of Pharmacovigilance experience can apply.

Senior Analyst – Drug Information & Risk Management

Job Summary

The Senior Analyst will work as part of a multidisciplinary team of healthcare professionals supporting Apotex products in domestic and international markets.

The role involves coordinating the development of medical documents such as Risk Management Plans and Risk Evaluation Mitigation Plans, while providing medical information related to the safe and effective use of drugs manufactured and marketed by Apotex Inc. and its affiliates and distributors worldwide.

Job Role & Responsibilities

The selected candidate will be responsible for:

• Provide verbal and written responses to medical inquiries from healthcare professionals, sales representatives, and other internal customers regarding Apotex products.
• Evaluate, analyze, and respond to medical inquiries accurately, objectively, and in a timely manner.
• Coordinate the preparation and updating of Risk Management & Risk Evaluation Mitigation Plans globally.
• Provide input into the medical sections of these plans using relevant regional templates.
• Apply technical and scientific skills to research and interpret medical information.
• Create and peer review new and revised medical information documents, including:

  • Response documents
  • Recall Q&As
  • Bulletins
  • Other medical information documents

• Participate in departmental and cross-functional business teams.
• Support team initiatives and contribute to team goals and projects according to business priorities.
• Ensure compliance with SOPs relating to adverse event and quality complaint reporting.
• Maintain awareness of current therapeutics and industry-based medical information regulations.
• Provide on-call coverage as per the assigned schedule.
• Assist in the preparation of reports.
• Update and maintain product databases and files as required.
• Work as a member of a team to achieve assigned outcomes.
• Perform work in accordance with established regulatory, compliance, and safety requirements.
• Perform other duties and special projects, including after-hours coverage of the DISPedia unit, as assigned.
• Work safely and collaborate with team members to achieve business outcomes.
• Demonstrate organizational values of Collaboration, Courage, Perseverance, and Passion.
• Maintain personal adherence to applicable compliance programs, including Global Business Ethics and Compliance, Global Quality, Safety and Environment, and HR policies.
• Perform other relevant duties as assigned.

Eligibility & Qualifications

Educational Qualification

The job posting lists the following qualifications:

• Bachelor of Pharmacy (B.Pharm)
• B.Sc. or Diploma in Health/Science-related discipline
• Master of Pharmacy (M.Pharm)
• Bachelor of Dental Surgery (BDS)

Experience

1–3 years of experience in Pharmacovigilance

Eligible Qualification Courses

B.Pharm | M.Pharm | B.Sc. | BDS | Diploma in Health/Science-related Discipline

Required Knowledge & Skills

Candidates should have:

• Excellent oral and written communication skills.
• Knowledge of Microsoft Office software, including:

  • Excel
  • PowerPoint
  • Word
  • Outlook

• Knowledge of Arisg Safety Database
• Knowledge of MedDRA
• Knowledge of Argus
• Knowledge of Embase
• Knowledge of MLM database
• Knowledge of online literature searching and review.

Pharmacovigilance & Medical Information

The position involves activities related to:

• Pharmacovigilance
• Medical Information
• Medical Inquiry Management
• Risk Management Plans
• Risk Evaluation Mitigation Plans
• Adverse Event Reporting
• Quality Complaint Reporting
• Medical Literature Searching
• MedDRA
• Argus
• Arisg Safety Database
• Embase
• Safety Information
• Regulatory and Compliance Requirements

Job Location & Details

Company: Apotex

Job Title: Senior Analyst – Drug Information & Risk Management

Location: Mumbai, Maharashtra – 400079

Date: 23 September 2026

Experience: 1–3 years in Pharmacovigilance

Job Type: Full Time

How to Apply

Interested and eligible candidates can apply online through the official Apotex Careers portal.

Apply Now – Apotex Senior Analyst, Drug Information & Risk Management

For inquiries regarding the job posting:

Email: rpalkar@apotex.co.in

Job Summary