Role & responsibilities
- Manage document control activities, including issuance, revision, archival, and maintenance of quality documents.
- Review and approve SOPs, specifications, testing procedures, batch records, COAs, ATRs, and laboratory documentation.
- Handle QMS activities, including deviations, CAPA, change controls, OOS, incidents, and audit trail reviews.
- Support vendor qualification, customer queries, internal audits, and customer/regulatory inspections.
- Conduct IPQA rounds to ensure compliance with GMP and quality systems.
- Review equipment qualification documents and support batch release of finished products.
- Review and approve raw material and packaging material documentation.
- Ensure compliance with GMP, quality standards, and regulatory requirements.

Preferred candidate profile
- Bachelor's/Master's degree in Pharmacy, Chemistry, Life Sciences, or related field.
- 5+ years of experience in Document Quality Assurance (DQA) in the pharmaceutical industry.
- Strong knowledge of GMP, QMS, documentation practices, and regulatory compliance.
- Positive analytical, documentation, and communication skills with attention to detail.
- Preferred Male Candidates

📌 Executive / Senior Executive - Document Quality Assurance (DQA - API) (Bengaluru)
🏢 Eurofins Advinus
📍 Bengaluru