We are hiring a Senior Executive APQR with 7–10 years of relevant pharmaceutical QA experience.

Key Responsibilities:

- Prepare and review Annual Product Quality Reviews (APQR/PQR) as per SOPs.
- Compile and analyze manufacturing, analytical, and QMS data (Deviations, OOS, OOT, CAPA) for trend analysis and risk assessment.
- Ensure APQR documentation is complete, accurate, compliant, and audit-ready.
- Review quality documents and maintain document control in line with GMP/GDP requirements.
- Identify process improvement opportunities and support closure of APQR action items.
- Support internal and external audits related to APQR and documentation.

Key Skills:

- Strong knowledge of APQR/PQR, GMP, and GDP documentation.
- Experience in data trending, technical document review, and quality compliance.
- Excellent analytical skills with a robust attention to detail and audit readiness.

Preferred Profile:

- Candidates with experience in EU-approved pharmaceutical manufacturing facilities are preferred.

📌 ODF APQR (Baddi)
🏢 Selective Global Search
📍 Baddi