AVENZA PHARMACEUTICALS PRIVATE LIMITED is looking for young and dynamic professionals from the Pharmaceuticals (OSD Formulation) background with proven experience in regulated markets (MHRA/USFDA/EU-GMP) for our Quality Control Team in Vadodara.
🔹 Open Positions:
1️⃣ GLP (4–8 years | Male only)
• SOP preparation
• Qualification of instruments
• Standard managements
2️⃣ HPLC – Open Lab (4–7 years | Male only)
• Chromatography expertise
• In-depth knowledge of open lab operations
• Audit trail review
• Reporting template creation
• Processing & calculation of chromatograms
3️⃣ QMS (5–8 years)
• Change Control, Deviation, CAPA & Investigations
• Impact & risk assessments
4️⃣ QC Investigation (4–6 years | Male only)
• Handling OOS, OOT, Pharma OOC
• Investigation & report preparation
5️⃣ RM/PM Analyst (2–3 years | Male only)
• Excipient & API analysis (EP/BP/USP/IP)
📌 Location: Vadodara
📌 Immediate joiners preferred
📧 Apply Now – Send your updated resume to:
👉 seema@avenzapharma.com
(Subject line: Application for QC–GLP/QMS/etc.)
At Avenza, we believe in quality, precision, and teamwork – join us and be a part of our growing journey in regulated markets!
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