Amneal Hiring Senior Executive / AM – Quality Assurance Role | Top Pharma QA Job | Apply Now
Looking for an exciting opportunity in the pharmaceutical industry? This Pharma Freshers Job update brings an excellent opening at Amneal Pharmaceuticals for the position of Senior Executive / AM – Quality Assurance in Ahmedabad, Gujarat. Candidates with experience in sterile manufacturing plants and qualifications like B.Pharma or M.Pharma can explore this promising Quality Assurance Careers opportunity with a leading pharmaceutical company.
- Job Title: Senior Executive / AM – Quality Assurance
- Location: Ahmedabad City, Gujarat, India
- Job Identification: 5023
About the Company
Amneal Pharmaceuticals is a globally recognized pharmaceutical company known for developing, manufacturing, and distributing high-quality medicines across multiple therapeutic segments. The company focuses on innovation, compliance, and advanced manufacturing practices while offering excellent career growth opportunities for pharmaceutical professionals.
Job Description
Applications are invited for the position of Senior Executive / AM – Quality Assurance for the IPQA department of a sterile manufacturing plant at Amneal. This Pharma QA Job is ideal for candidates experienced in Quality Assurance operations, batch documentation review, process validation, environmental monitoring, and cGMP compliance.
Key Responsibilities
- Perform line clearance before dispensing, manufacturing, filling, inspection, labeling, sealing, and packing activities.
- Review BMRs and BPRs for batch release approval.
- Handle process validation, cleaning validation, hold time study, media fill, and routine batch sampling as per SOPs.
- Conduct in-process quality checks during manufacturing stages.
- Monitor environmental conditions, water trends, and clean room activities.
- Review calibration certificates and reports like CIP, SIP, autoclave, and filter integrity printouts.
- Ensure cGMP compliance on the production floor.
- Manage environmental monitoring materials such as plates, swabs, and samplers with microbiology coordination.
- Perform environmental monitoring, non-viable particle monitoring, compressed air/nitrogen monitoring, and personnel monitoring.
- Participate in media fill simulations and manufacturing qualification activities.
- Monitor aseptic practices of operators during sterile manufacturing operations.
Qualifications
- Education: B.Pharma, M.Pharma
- Total Experience: 2 – 7 years in the IPQA Department of the sterile manufacturing plant
