Amneal Pharma Hiring for Quality Assurance – AGM Role

Amneal Pharmaceuticals is actively hiring for the position of Assistant General Manager (AGM) – Quality Assurance for its cutting-edge sterile manufacturing site located in Pipan, Ahmedabad. This is a high-impact leadership role designed for candidates who are passionate about maintaining regulatory excellence and driving operational quality in a USFDA-approved facility.

About Amneal Pharmaceuticals

Amneal Pharmaceuticals, Inc. (NYSE: AMRX) is a global, integrated pharmaceutical leader committed to improving lives through accessible and affordable medicine. With over 7,500 employees worldwide and a robust portfolio of 270+ high-quality medicines, Amneal operates with a mission to make healthy possible. The company’s focus on research, innovation, and compliance has positioned it as a trusted name in the pharmaceutical industry.

Job Role: AGM – Quality Assurance

Job Location: Pipan, Ahmedabad

Department: Quality Assurance – Sterile/Injectable Manufacturing

Job Type: Full-time | On-site

Key Responsibilities

As the AGM of QA, you will play a pivotal role in ensuring that all quality systems and procedures align with global regulatory expectations, especially those set by USFDA and other health authorities. Your core responsibilities will include:

• Leading and mentoring the QA team to foster a culture of continuous improvement.
• Ensuring quality compliance across manufacturing and quality operations.
• Overseeing regulatory and internal audit readiness, including timely CAPA implementation.
• Approving and releasing manufactured sterile injectable batches within timelines.
• Managing market complaint investigations with comprehensive root cause analysis and impact assessments.
• Supervising qualification and validation of equipment, utilities, and facilities.
• Collaborating with cross-functional teams to uphold product integrity and process excellence.

Candidate Profile

Educational Qualification: B Pharm or M.Pharm from a recognized institution.

Experience Required:

• 15 to 18 years of hands-on experience in a Quality Assurance role at a sterile/injectable manufacturing site.
• Prior exposure to USFDA-approved facilities is a must.
• Strong leadership, documentation, audit-handling, and compliance background.

Preferred Traits: Strategic thinker with the ability to lead quality improvement initiatives.

Excellent communication and decision-making skills.

Proven track record in regulatory inspections and successful batch releases.

How to Apply

If you meet the qualification criteria and are ready for a leadership challenge, send your updated CV to:

Ajaykumar.pandey@amneal.com