Apply for Amneal IPQA Executive Job | QA Opportunity for Pharmacy Professionals
Looking for a Pharma QA Job with a leading pharmaceutical company? Amneal Careers has announced an exciting opportunity for the position of Executive, IPQA in Ahmedabad, Gujarat. This role is ideal for B.Pharm and M.Pharm professionals seeking experience in GMP compliance, quality assurance operations, batch documentation review, validation activities, and regulatory compliance within pharmaceutical manufacturing.
- Position: Executive, IPQA
- Location: Ahmedabad City, Gujarat, India
About the Company
Amneal Pharmaceuticals is a global pharmaceutical company committed to delivering high-quality medicines and maintaining the highest standards of quality, compliance, and patient safety. Through Amneal Careers, professionals can build rewarding careers in pharmaceutical manufacturing, quality assurance, and regulatory compliance.
Job Description
The role is responsible for ensuring day-to-day compliance with global GMP (Good Manufacturing Practices) during manufacturing, packing, and dispensing activities at the site. The role provides on-floor quality assurance support, ensuring operations are performed as per approved procedures, validated processes, and regulatory expectations.
Key Responsibilities
- Monitor manufacturing and packing activities to ensure compliance with GMP and quality standards.
- Perform In-Process Quality Assurance (IPQA) checks during production operations.
- Conduct line clearance and verify the readiness of manufacturing, packing, and dispensing areas.
- Review batch records, batch manufacturing records (BMR), batch packing records (BPR), and certificates of analysis (COA) before batch release.
- Maintain and review quality-related records, including equipment logbooks, dispensing logs, calibration records, and environmental monitoring records.
- Coordinate with the IPQC team and perform routine in-process checks.
- Ensure compliance with regulatory requirements, including 21 CFR Part 210 & 211 guidelines.
- Monitor environmental conditions and support cleaning, sterilization, and aseptic operations.
- Assist in cleaning validation, process validation, and media fill (aseptic process simulation) activities.
-
Ensure
adherence to Good Documentation Practices (GDP) and data integrity requirements.
- Participate in GMP inspections, audits, investigations, and compliance reporting activities.
- Train shop-floor personnel on GMP requirements, quality standards, and documentation practices.
- Maintain IPQA documents and records in an audit-ready state.
- Communicate effectively with cross-functional teams and support continuous quality improvement initiatives.
Qualifications
- Education: B. Pharm – Required/ M. Pharm – Preferred
- Experience: 1 year or more in 1 – 4 Years
Required Skills
- Batch Documentation Record & Review
- Change & Deviation Control
- Deviation Control & Compliance
- Effective Communication
- GMP & Regulatory Compliance Oversight
- Good Documentation Practices (GDP)
- In-Process Checks
- Process Monitoring & Control
- Quality Risk Analysis & Control
- Risk Assessment & Control
