QA Jobs in Ahmedabad | Senior Officer Role at Amneal Pharmaceuticals – Microbiology Graduates Apply
Looking for QA Jobs in Ahmedabad? Join Amneal Pharmaceuticals, a global leader in the pharmaceutical industry, as a Senior Officer, QA Environment Monitoring. This exciting opportunity is ideal for professionals passionate about quality assurance, environmental monitoring, and compliance in sterile manufacturing. Start your rewarding career journey with one of the top jobs at Amneal, where innovation meets excellence.
- Job Position: Senior Officer, QA Environment Monitoring
- Location: Ahmedabad City, Gujarat, India
About the Company
Amneal Pharmaceuticals is a trusted name in the global healthcare industry, offering exciting jobs at Amneal for professionals looking to build a career in pharmaceutical quality and compliance. Known for its innovation, integrity, and commitment to patient safety, Amneal provides an excellent work environment for those seeking long-term QA Jobs in Ahmedabad.
Qualifications
Education:
B.Sc./M.Sc in Microbiology
Experience:
1–6 years of experience in Environmental Monitoring within a sterile manufacturing plant.
Internal Applicants:
Must have completed at least 2 years in their current role before applying.
Job Description
If you are exploring QA Jobs in Ahmedabad, this role offers a chance to contribute to quality assurance excellence. As a Senior Officer in QA Environment Monitoring, you will oversee environmental monitoring activities and ensure compliance with cGMP regulations in sterile manufacturing areas. This position at Amneal involves coordinating line clearance operations before dispensing, manufacturing, filling, inspection, sealing, labeling, and packaging.
Key Responsibilities
For this QA Job Role in Ahmedabad, the key responsibilities are:
- Execute line clearance activities before various manufacturing operations.
- Perform and review environmental monitoring activities and EM data.
- Conduct process validation, cleaning validation, and batch sampling per SOP.
- Review executed BMRs, BPRs, and calibration certificates.
- Oversee the issuance and reconciliation of EM materials, including plates and swabs.
- Participate in media fill simulation studies and qualification activities.
- Monitor non-viable particles, compressed air, and nitrogen gas.
- Maintain cGMP and GDP compliance on the shop floor.
- Review CIP, SIP, autoclave, and filter integrity printouts.
- Ensure documentation accuracy and compliance with QA standards.
Skills Required
- Environmental Monitoring (EM) – Expert
- In-Process Quality Controls (IPQC) & Sampling – Practitioner
- Aseptic Process Simulation (Media Fill) – Expert
- Line Clearance & Batch Record Review – Practitioner
- Good Documentation Practices (GDP) – Practitioner
- Regulatory & Compliance Knowledge – Practitioner
