Quality Control

Roles & Responsibilities:
• Perform AMV and Process Validation (PV) sample analysis as per approved protocols
• Execute sample planning, analysis, and data review activities
• Conduct routine and stability analysis of Raw Materials (RM), Packing Materials (PM), and Finished Products (FP)
• Carry out analytical Method Validation and verification
• Operate and maintain sophisticated analytical instruments including HPLC, Dissolution, GC, UV, and FTIR
• Ensure adherence to cGMP, data integrity, and laboratory safety requirements
• Prepare, review, and maintain analytical documentation and laboratory records
• Support audits, investigations, and regulatory inspections

Qualification:
• B.Sc/M.Sc / B.Pharm / M.Pharm (relevant discipline)

Experience:
• 1–10 years of experience in Quality Control (Pharma / Formulations)
• Freshers may be considered for entry-level QC roles
• Preference for candidates with hands-on instrument exposure (male candidates preferred as per site requirements)

Skills:
• Strong knowledge of pharmaceutical QC testing and analytical techniques
• Hands-on experience with HPLC, Dissolution, GC, UV, and FTIR
• Understanding of AMV, PV, RM/PM/FP testing, and method validation
• Familiarity with cGMP, GLP, and data integrity principles

About the Organization:
Theon Pharmaceuticals Ltd is a WHO-GMP certified pharmaceutical company with advanced manufacturing facilities in Nalagarh (HP) and Derabassi (Punjab), specializing in high-quality formulations and CDMO services.

Walk-in Interview Details:
• Date: 15 February 2026
• Time: 10:00 AM onwards
• Venue: Hotel Gianz, Baghbhania, Baddi–Nalagarh Highway (NH21), Baddi, Himachal Pradesh – 174103
• Carry: Updated resume, last three salary slips, latest increment letter (if applicable)