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Pharmacovigilance Quality Assurance

3+ years
₹6–10 LPA
10 July 26, 2025
Job Description
Job Type: Full Time Education: PhD / Pharm D / M.Pharm / B.Pharm / BDS / B.Tech / M.Tech / M.Sc. / B.Sc. (Life Sciences) Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Pharmacovigilance Quality Assurance – Wipro
Location: Pune
Work Mode: Work From Office
Shift: General Shift
Work Type: Full-time
Estimated Salary: ₹6–10 LPA (based on experience and current industry benchmarks)


About the Role:
Wipro is actively hiring for a Pharmacovigilance Quality Assurance (PVQA) position at its Pune location. This role involves managing PV quality activities including document control, metrics reporting, CAPA tracking, training oversight, and audit support. The ideal candidate will have prior experience in pharmacovigilance quality management—not in ICSR case processing or GMP/manufacturing QA.


Eligibility Criteria:

Qualifications:

  • PhD / Pharm D / M.Pharm / B.Pharm

  • BDS / B.Tech / M.Tech (Life Sciences)

  • M.Sc. / B.Sc. (Life Sciences)

Experience:

  • 3–6 years of total experience

  • Minimum 3 years of relevant experience in Pharmacovigilance or Drug R&D Quality Management

Note: Candidates only from ICSR case processing or GMP/manufacturing QA backgrounds are not eligible.


Key Skills Required:

  • Solid understanding of Good Pharmacovigilance Practices (GVP)

  • Knowledge of audit procedures and regulatory compliance in PV

  • Hands-on experience in quality management systems (QMS)

  • Strong documentation and communication skills


Roles & Responsibilities:

  1. Maintain and regularly update quality trackers.

  2. Share periodic PV metrics with internal stakeholders.

  3. Ensure controlled documents are current and comply with applicable SOPs.

  4. Prepare and review deviations and Corrective and Preventive Actions (CAPAs).

  5. Maintain and document all training records, including induction, on-the-job, and refresher trainings.

  6. Liaise effectively with internal teams and stakeholders.

  7. Record and circulate meeting minutes in a timely manner.

  8. Monitor updates in regulatory guidelines and communicate them internally.

  9. Assist in internal audits and support external regulatory inspections.

  10. Oversee local training activities.

  11. Perform additional PVQA duties as assigned by the lead/manager.


How to Apply:
Interested candidates can email their resumes to:
📩
varsha.kamalapurkar@wipro.com