Full Time

Production - Documentation (Pharmacy)

Covalent Laboratories

Hyderabad

Salary Not Disclosed

Posted 19/02/2026

About the Role

Roles & Responsibilities
• Prepare and review production documents including BMR/BPR and SOPs
• Ensure accurate documentation aligned with GMP standards
• Coordinate with Production and QA for compliance activities
• Support audits and regulatory inspections

Qualification
• B.Sc / Bachelor's degree in Pharmacy

Experience
• 2–4 years in production documentation (API manufacturing preferred)

Skills
• Strong GMP knowledge
• Documentation control and review expertise
• Attention to detail and compliance orientation

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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