Full Time

Quality Control (HPLC, GC)

Covalent Laboratories

Hyderabad

Salary Not Disclosed

Posted 19/02/2026

About the Role

Roles & Responsibilities
• Perform analytical testing using HPLC and GC instruments
• Conduct routine analysis of raw materials, intermediates, and finished APIs
• Prepare and maintain analytical documentation
• Ensure compliance with regulatory and data integrity standards

Qualification
• M.Sc / Master of Pharmacy / Bachelor of Pharmacy

Experience
• 2–4 years in Quality Control (API industry preferred)

Skills
• Hands-on experience with HPLC and GC
• Strong analytical and documentation skills
• Knowledge of GMP and regulatory requirements

About the Company
Covalent Laboratories is a WHO-GMP and USFDA-approved manufacturer specializing in Cephalosporin APIs and intermediates, known for its regulatory-compliant manufacturing standards and strong presence in global pharmaceutical markets.

Walk-In Interview Details
Dates: 23 February 2026 – 24 February 2026
Venue: Covalent Laboratories, Gundla Machnoor, Sangareddy, Telangana
Documents to Carry:
• Updated Resume
• Educational Certificates
• Experience Letters
• Recent Passport-Size Photographs

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