- Location: Pune | Mandideep | Goa | Nagpur | Pithampur | Nashik
- Experience:
- 1–5 Years
Key Responsibilities:
- Validate QC systems/software as per GAMP & 21 CFR Part 11.
- Execute the complete Validation Lifecycle.
- Perform IT QMS activities (Change Control, CAPA, Deviations, etc.).
- Support Equipment Qualification (IQ/OQ/PQ).
- Prepare and maintain CSV documentation.
- Ensure compliance with GMP and regulatory requirements.
Requirements:
- 1–5 years of CSV experience in the Pharma/Life Sciences industry.
- Strong knowledge of GAMP and 21 CFR Part 11.
- Good documentation and communication skills.
- Experience with QC systems/software validation is preferred.
Pay: ₹300,000.00 - ₹600,000.00 per year
Benefits:
- Health insurance
- Leave encashment
- Life insurance
- Provident Fund
Work Location: In person
