JAMP- Interview for Pharmacovigilance (PV) on 18th February, 2024
18th February, 2024 (Sunday)
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.
Date & Day:
18th February, 2024 – Sunday
Time:11:00 AM to 04:30 PM
Venue: JAMP India Pharmaceuticals Pvt. Ltd.,
A-1207, 12th Floor, Navratna Corporate Park, Ambli Bopal road, Ambli, Ahmedabad-380058
Department: Pharmacovigilance (PV)
Qualification:M.Pharm / M.Tech / M.Sc / B.Pharm / B.Tech / B.Sc
(or relevant qualification in Life Sciences)
Candidates with Experience in Pharmacovigilance, Drug Safety, Life Sciences, Medication Surveillance, Drug Efficiency & Safety or relevant domain are only requested to apply
AGM/12-15 yrs(1 Position)
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) 8-10 yrsEffectively 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) 4-7 yrs
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)1-3 yrs(4 positions)
Performs Data entry in Argus safety database for ICSR from all sources including: Tracking of received ICSR
–
Entry of ICSR into JAMP safety database
Query management
Performs consistent coding to coding conventions, including MeDRA.
Generates concise, accurate and well-written case narratives.
Reviews cases for quality, consistency and accuracy, including review of peer reports.
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 d.thaker@jamppharma.com
or scan the QR code as mentioned below and apply.
Scan & apply online
• Please note that JAMP India Pharmaceuticals Pvt. Ltd. does not hire through consultants / agents who promise interviews / jobs for monetary consideration/registration fees. Beware of such fraudulent calls.
Contact Person: Mr. Dakshesh Thaker (HR)
www.jamppharma.com
