QA Executive at Sun Pharmaceutical – M.Pharm candidates – Apply Now!
Are you a detail-oriented M. Pharm graduate with 2-3 years of experience in Pharmacovigilance Quality Assurance or Pharmacovigilance operations? Sun Pharmaceutical Industries Ltd, a leading pharmaceutical company, is seeking a dedicated Executive – Taro QA PV Oversight to join our R&D Quality team in Gurgaon. If you have a strong understanding of GVP modules and a passion for ensuring the quality and compliance of Pharmacovigilance activities, we encourage you to apply!
Job Posting: Executive- Taro QA PV oversight
- Position: Executive – R&D Quality, GPvP-QA ,Pharmacovigilance as PV-QA auditor
- Grade: G12A
- Number of Positions: 2
- Job Location: Gurgaon
- Department: R&D Quality
Job Responsibilities:
As an Executive – Taro QA PV Oversight at Sun Pharmaceutical Industries Ltd, your responsibilities will include:
- Assisting in developing global Pharmacovigilance system auditing program and responsible for conducting and reporting audits being a lead auditor/co-auditor for outsourced parties (CROs, Service Providers, Vendors), Affiliates & Partners etc., associated with Sun Pharma Pharmacovigilance operations.
- Assisting in conducting and reporting audits being a lead auditor/co-auditor for Sun Pharma sites associated with Pharmacovigilance activities/ operations to assure adequacy & adherence with established Quality Systems.
- Assisting for the preparation and maintenance of CAPA tracker and assure that the CAPAs are adequately addressed and closed.
- Being responsible for the review of Pharmacovigilance SOPs for completeness, clarity, and compliance to global/regional policies, and applicable regulatory regulations & guidelines.
- Maintaining up to date and in accordance with global expectation a quality system supporting companies supporting PI management.
- Reviewing PSMFs of assigned countries.
- Providing support in risk assessment of business partners.
- Participating during qualification of identified vendors for Pharmacovigilance support.
- Managing the Internal Audit Observation Database (IAOD) with the perspective of sharing audit reports, CAPA reports and observation of global impact with all internal regional PV sites across the globe and Global Pharmacovigilance.
Desired Candidate Profile:
- M.Pharm with 2-3 years of experience in PV-QA or Pharmacovigilance operations.
- It is preferred if well aware about GVP modules.
- Good oral and written communication skills.
Keywords: Pharmacovigilance Quality Assurance, PV QA, Auditing, R&D Quality, RQA, Pharmacovigilance, Pharmacovigilance Quality Assurance, Auditing, R&D Quality, RQA, and marketed product
