NonaGen Lifesciences Pvt. Ltd. is establishing a state-of-the-art sterile pharmaceutical manufacturing campus focused on Large Volume Parenterals (LVP), with a long-term vision of expanding into Small Volume Parenterals (SVP), advanced sterile injectables, prefilled syringes, cartridges and global Contract Development & Manufacturing (CDMO) services.
We are assembling the Founding Leadership Team that will design, commission and operate our manufacturing campus from the ground up. This is a rare prospect to build systems, culture and operational excellence from day one while contributing to the long-term growth of an export-oriented pharmaceutical company.
Key Responsibilities
Establish and lead the Quality Management SystemDevelop QA policies,
SOPs and compliance frameworksLead validation, deviations, CAPA and change controlEnsure Data Integrity and cGMP complianceLead internal, customer and regulatory auditsPrepare the site for WHO-GMP and future international inspectionsBuild and mentor the Quality organisation from inceptionRequirements
M.Pharm / B.Pharm or equivalent18–25 years in sterile pharmaceutical QAExperience with injectables manufacturingStrong knowledge of WHO, USFDA, MHRA or EU-GMP expectationsGreenfield project experience preferredPay: ₹4,200,000.00 - ₹4,800,000.00 per year
Perks:
Food providedHealth insurancePaid sick timeWork Location: In person
📌 Head – Quality Assurance & Regulatory Compliance Mumbai
🏢 Udit Group of Companies
📍 Mumbai
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