Eurofins Advinus, a globally reputed pharmaceutical research and testing organization, is hiring a QMS Documentation Specialist for its US FDA–audited GMP Testing Laboratory in Bangalore.
This role is ideal for experienced QA/QMS professionals who excel in GMP documentation, investigations, and regulatory compliance.
🧾 Key Responsibilities
- Draft, review, and manage GMP-controlled documents
- Handle Deviations, Change Controls, and CAPAs with timely closure
- Perform and document OOS / OOT investigations
- Prepare technical and investigation reports aligned with global regulatory standards
- Ensure continuous compliance with US FDA & GMP guidelines
🎓 Eligibility Criteria
- Education: M.Sc / M.Pharm (Life Sciences, Chemistry, or related discipline)
- Experience: 3–8 years in QA/QMS within a GMP laboratory
- Skills Required:
- Strong hands-on experience in CAPA & Change Management
- Excellent technical writing & documentation skills
- Sound understanding of GMP quality systems
📍 Job Location
- Bangalore, India
📧 How to Apply
Interested and eligible candidates can share their updated CV at:
📩 Sekhar.Sompalli@advinus.eurofinsasia.com
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📌 Email Subject (Mandatory):
QMS Documentation Specialist (GMP Testing Laboratory)
🔁 Referrals are welcome – share this opportunity with your QA/QMS network.
