Pharma QA Job at Amneal Careers | Associate IPQA Role | Pharma Graduates | Apply Now
Looking for a rewarding Pharma QA Job with Amneal Careers? This Associate IPQA opportunity in Ahmedabad, Gujarat, is ideal for candidates seeking growth in pharmaceutical quality assurance, GMP compliance, and manufacturing operations. Through Amneal Careers, professionals with a B. Pharm qualification can gain valuable exposure to IPQA activities, documentation practices, and regulatory standards in a leading pharmaceutical environment.
- Position: Associate, IPQA
- Location: Ahmedabad City, Gujarat, India
- Job ID: 7806
About the Company
Amneal Careers provides opportunities for pharmaceutical professionals to work in GMP-regulated manufacturing environments focused on quality, compliance, and operational excellence. The company emphasizes regulatory compliance, data integrity, quality systems, and continuous improvement to ensure the delivery of safe, high-quality pharmaceutical products.
Job Description
- Ensure compliance with global GMP guidelines during manufacturing, packing, and dispensing activities
- Perform real-time quality checks and line clearance on the shopfloor
- Monitor manufacturing processes to ensure products meet approved quality standards
- Verify cleaning, sterilization, and aseptic operations regularly
- Maintain accurate documentation and ensure data integrity compliance
- Support process validation and cleaning validation activities
- Assist in aseptic process simulations and quality monitoring
- Help in deviation handling, risk management, and audit preparedness
- Ensure safe, high-quality pharmaceutical products are consistently manufactured
Key Responsibilities
- Perform IPQA (In-Process Quality Assurance) checks during manufacturing and packing operations
- Execute and document Line Clearance and Readiness for manufacturing, packing, and dispensing
- Conduct In-Process Checks & Sampling (In-process, Stability & ANSI)
- Ensure compliance with 21 CFR Part 210 & 211 (Code of Federal Regulations – Current Good Manufacturing Practice for Drugs)
- Review BMR (Batch Manufacturing Record) and BPR (Batch Packing Record) for accuracy and completeness
- Ensure Good Documentation Practices (GDP – Good Documentation Practices) compliance.
Qualifications
- Education: B. Pharm – Preferred
- Experience: 1 year or more in 1 – 4 Years
Specialized Knowledge & Licenses:
- Calibration
- Data Entry
- Detail Oriented
- Facility Inspection
- First Article Inspections
- Good Manufacturing Practices
- Investigation
- Laboratory Information Management Systems
- Quality Management Systems
- United States Pharmacopeia (USP) Compliance
- Visual Inspections
