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JAMP group Inviting proficient Pharmacovigilance experts


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JAMP group Inviting proficient Pharmacovigilance experts

The JAMP group is a proud Canadian owned company with its international headquarters located in Boucherville, 20 minutes from downtown Montreal, Quebec, Canada. The JAMP Pharma Group is active in all sectors of the pharmaceutical industry with our JAMP Pharma Generics, Orimed branded products, our Wampole and Laboratoire Suisse natural health supplements and our Cosmetic Import beauty and personal care products. The JAMP Pharma Group has also made a major investment in biosimilars which is one of the fastest growing markets in the pharmaceutical industry.

Inviting proficient Pharmacovigilance (PV) experts! Seize the opportunity as we are building and establishing our new pharmacovigilance team in Ahmedabad. Contribute to excellence and chart the course for advancing drug safety with us.

Department : Pharmacovigilance (PV)
Candidates with Experience in Pharmacovigilance, Drug Safety, Life Sciences, Medication Surveillance, Drug Efficiency & Safety or relevant domain are only requested to apply
Qualification : M.Pharm / M.Tech / M.Sc / B.Pharm / B.Tech / B.Sc

(1 Position)
Experience : 12-15 yrs
Key Roles : • Responsible as a Subject Matter Expert and leading the PV team in India.
•  Provides technical and process oversight with respect to the current processes.
•  Prepares and maintains key performance indicators (KPIs) and compliance metrics covering safety activities for the PV department in India.
•  Reviewed compliance for activities.
•  Promotes Good Pharmacovigilance Practices (GvP).

Assistant Manager / Manager
(Case Processing and/or Periodic Reports, Literature, Reconciliation) (3 positions)
Experience : 8-10 yrs
Key Roles : • Effectively maintains the safety database and relevant coding conventions to ensure quality control and performs quality review.
• Performs reconciliation activities with Global PV team.
• Perform quality controls the reportability assessment of ICSR.
• Authors or reviews safety reports.
• Performs internal and external reconciliation activities.
• Support for the management of safety reports, reconciliation and literature schedules.
• Performs quality control activities related to reconciliation, literature and safety reports preparation.

Executive / Senior Executive
(Case Processing and/or Periodic Reports, Literature, Reconciliation) (5 positions)
Experience : 4-7 yrs
Key Roles : • Performs ICSR triage (serious, non-serious or non-valid reports).
• Supports reconciliation activities related to case processing with Global PV team.
• Authors safety reports including Periodic Safety Update Reports (PSURs) and Periodic Benefit-Risk Evaluation Report (PBRERs).
• Review weekly literature.
• Performs day-to-day PVG activities.
• Review regulatory / pharmacovigilance publications and information sources in order to stay updated on current regulations, practices, procedures and proposals.

Officer (Case Processing)
(4 positions)
Experience : 1-3 yrs
Key Roles : • Performs Data entry in Argus safety database for ICSR from all sources including:
- Tracking of received ICSR
- Entry of ICSR into JAMP safety database 1-3 yrs - Query management
• Generates concise, accurate and well-written case narratives.
• Performs consistent coding to coding conventions, including MeDRA.
• Reviews cases for quality, consistency and accuracy, including review of peer reports.

Date & Day : 18th February, 2024 - Sunday
Time : 11:00 AM to 04:30 PM
Venue : lndia Pharmaceuticals Pvt. Ltd., A-1207,12th Floor, Navratna Corporate Park, Ambli Bopal road, Ambli, Ahmedabad - 380058

Interested candidates can Walk-in for interview along-with their updated resume, passport size photograph and relevant documents.
Candidates who are unable to attend the interview can send their profile at
or apply online mentioned below link and apply.

Apply Online

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