Sr Executive / Asstt Manager - Validation (QA Department)

As an experienced and dynamic professional in the pharmaceutical industry, you have the opportunity to join Ananta Medicare Ltd in Sri Ganganagar, Rajasthan, specifically in the Quality Assurance Department for Validation activities in a manufacturing facility. Your role will involve 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 - 2-6 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 passionate about contributing to a growing pharmaceutical organization and possess the required qualifications and experience, we encourage you to connect with us by sharing your CV at hr1@anantamedicare.in. Feel free to share this opportunity with someone who might be interested in this role. #PharmaJobs #Validation #QualityControl #SterileManufacturing #Cepha #PharmaceuticalIndustry #Hiring #AnantaMedicare #SriGanganagar,