Quality Assurance
About the Role
Roles & Responsibilities:
• Perform Analytical QA and Lab QA activities as per cGMP requirements
• Conduct vendor audits for raw materials and packing materials
• Handle QA documentation including SOPs, APQR, risk assessment, and compliance records
• Execute and review Process Validation and Cleaning Validation activities
• Support internal audits, regulatory inspections, and quality reviews
• Ensure compliance with WHO-GMP and regulatory guidelines
• Coordinate with QC, Production, and cross-functional teams
Qualification:
• M.Sc / B.Pharm
Experience:
• 3–8 years of experience in Quality Assurance (Pharma / Formulations)
Skills:
• Strong knowledge of Analytical QA, Lab QA, and vendor audit processes
• Experience in validation, APQR, and risk management activities
• Good understanding of WHO-GMP and quality systems
• Strong documentation and communication skills
About the Organization:
Theon Pharmaceuticals Ltd is a WHO-GMP certified pharmaceutical company with manufacturing units in Himachal Pradesh and Punjab, specializing in formulations and CDMO services for domestic and global markets.
Walk-in Interview Details:
• Date: 15 February 2026
• Time: 10:00 AM onwards
• Venue: Hotel Gianz, Baghbhania, Baddi–Nalagarh Highway (NH21), Baddi, HP – 174103
• Carry: Updated CV, last 3 salary slips, latest increment letter (if applicable)
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