Company: NonaGen Lifesciences Pvt. Ltd.

About NonaGen Lifesciences

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 opportunity 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
- Strong 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)
🏢 NonaGen Lifesciences
📍 India