Medrich Pharma Recruitment for Experienced Pharmacovigilance Candidates
We have a requirement in PVQA.
Looking for candidates with 6-8 years of experience
Qualification is M Pharma.
The detailed role is mentioned below: Responsible for maintaining all aspects of the quality management system in pharmacovigilance.
Ensuring timeline and quality comply with legislation and quality assurance codes.
Identifying training needs and recommendations for annual training plan.
Maintaining, training, implementation, and quality review of PV SOPs.
Quality review of the Pharmacovigilance System Master File (PSMF).
Ensuring deviations are identified and the appropriate CAPAs are implemented.
Preparation of monthly report of pharmacovigilance activities.
Perform a six-monthly Quality check for individual case safety reports.
Perform quality review of regulatory documents (PSURS, RMP, ADCO, referrals and any other Health Authority requests etc).
Review of all PV trackers and folders.
Monitoring and auditing process of vendor and service provider. Coordinate for Business Continuity plan. Archiving of all PV-related documents as per the SOP.
Interested may share the profiles to aravinda.p@medreich.com, or sekhar.s@medreich.com
