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.Pharm2–6 years of experience in Qualification & Validation in Sterile Manufacturing (Injectable / Cephalosporin / Oncology preferred)Strong understanding of regulatory guidelines and documentation practicesHands-on experience with Autoclaves, Vial Washing, Tunnel Sterilizers, LAF, and HVAC Systems will be an added advantageIf 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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Skills Required
Cleaning Validation, Process Validation