QA Process Validation Assistant Manager Require at USV Private Limited

USV Private Limited is a prominent Indian multinational pharmaceutical and biotechnology company founded in 1961, specializing in diabetes and cardiovascular therapeutics. Headquartered in Mumbai, it is a market leader in Oral Anti-Diabetic (OAD) drugs and offers a diverse portfolio, including APIs, biosimilars, and injectables, alongside consumer healthcare products like Sebamed.

Post : Assistant Manager - Process Validation - QA

Job Description
1. Oversee the end-to-end execution and documentation of process validation, equipment qualification, and cleaning validation activities to ensure full regulatory compliance.
2. Draft, review, and approve critical quality documents, including Validation Master Plans (VMP), protocols, reports, Risk Assessments, and Standard Operating Procedures (SOPs).
3. Lead the investigation, root cause analysis (RCA), and impact assessment for market complaints received from customers and regulatory authorities.
4. Manage and evaluate quality deviations, Out of Specifications (OOS), and Out of Trends (OOT) related to manufacturing processes and market products.
5. Formulate, implement, and track Corrective and Preventive Actions (CAPA) arising from process failures, audit findings, and market complaints.
6. Conduct periodic Product Quality Reviews (PQR/APQR) to evaluate process consistency, trending, and product quality over time.
7. Coordinate cross-functionally with Production, R&D, QC, Regulatory Affairs, and Supply Chain to drive seamless validation runs and complaint resolutions.

8. Act as the primary Quality Assurance point of contact for internal quality audits, client audits, and health authority inspections (e.g., USFDA, EMA).
9. Define critical process parameters (CPPs) and critical quality attributes (CQAs) while implementing Quality by Design (QbD) principles across commercial products.
10. Monitor statistical process control (SPC) data and trends to identify potential process variations before they impact finished product quality.
11. Track and report key performance indicators (KPIs) and quality metrics related to process capabilities and complaint resolution timelines to senior leadership.
12. Ensure strict adherence to global cGMP standards, ICH guidelines, and regional regulatory requirements for all commercial and validated products.
13. Lead Risk Management initiatives (PFMEA) to identify, assess, and mitigate potential quality risks across drug product manufacturing processes.
14. Oversee the Change Control management system to assess the quality impact of raw material, process, or equipment modifications on product validation status.
15. Train and mentor junior QA staff on current validation practices, complaint handling procedures, and regulatory compliance standards.

Additional Information
Location : Vadodara (Savli)
Industry Type : Pharma/ Healthcare/ Clinical research
SBU : Operations
Function : Formulation Plant
End Date : 21 Nov 2026