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 System
Develop QA policies, SOPs and compliance frameworks
Lead validation,
deviations, CAPA and change control
Ensure Data Integrity and cGMP compliance
Lead internal, customer and regulatory audits
Prepare the site for WHO-GMP and future international inspections
Build and mentor the Quality organisation from inception
Requirements
M.Pharm / B.Pharm or equivalent
18–25 years in sterile pharmaceutical QA
Experience with injectables manufacturing
Solid knowledge of WHO, USFDA, MHRA or EU-GMP expectations
Greenfield project experience preferred
Pay: ₹4,200,000.00 - ₹4,800,000.00 per year
Advantages:
Food provided
Health insurance
Paid sick time
Work Location: In person
📌 Head – Quality Assurance & Regulatory Compliance India Mumbai
🏢 NonaGen Lifesciences
📍 Mumbai
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