Sr Executive / Asstt Manager - Validation (QA Department)

Preference to Immediate Joiner

Company: Ananta Medicare Ltd, Sri Ganganagar, Rajasthan

Ananta Medicare Ltd is looking for an experienced and dynamic professional to join our Quality Assurance Department for Validation activities in a manufacturing facility with hands-on experience in qualification and validation activities for a sterile / Cepha manufacturing setup.

Key Responsibilities:

Execution and review of Qualification activities for Equipment, Utilities, and Facilities (URS, DQ, IQ, OQ, PQ).

Preparation and review of validation protocols and reports (Process Validation, Cleaning Validation, Sterilization Validation, HVAC Qualification, etc.).

Coordination with Production, QC, and Engineering teams for timely execution of qualification/validation activities.

Handling periodic requalification and revalidation schedules.

Review of Change Control, Deviation, and CAPA related to qualification and validation.

Ensuring compliance with cGMP, WHO, EU, and USFDA guidelines.

Maintaining documentation as per regulatory requirements.

Desired Qualification & Experience:

B.Pharm / M.Pharm

26 years of experience in Qualification & Validation in Sterile Manufacturing (Injectable / Cephalosporin / Oncology preferred)

Strong understanding of regulatory guidelines and documentation practices

Hands-on experience with Autoclaves, Vial Washing, Tunnel Sterilizers, LAF, and HVAC Systems will be an added advantage

If you are a passionate professional eager to contribute to a growing pharmaceutical organization, we would love to connect!

Interested candidates may share their CVs at: [HIDDEN TEXT]

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