Senior Executive - Production (Qualification & Validation)

About the role

To support and execute qualification and validation activities related to production equipment, utilities, and processes in an Oral Solid Dosage (OSD) manufacturing facility, ensuring compliance with USFDA, cGMP, and regulatory requirements.

What you'll do

• Production areas and systems
• Prospective, concurrent, and re‑validation studies
• Prepare, review, and execute validation protocols and reports as per approved SOPs
• Ensure validation activities are completed within defined timelines
• Coordinate with Production, Engineering, QA, and QC teams during qualification and validation activities

What you need

• 6–8 yrs of experience
• ISO 9001
• GMP
• Technical writing
• HVAC
• FMEA
• SOP writing
• B.Pharm or M.Pharm

Good to have

• Internal audit