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. The role performs line clearance, in-process checks, routine area monitoring, and documentation review, ensuring data integrity, product quality, and patient safety. The position supports cleaning validation, process validation, and aseptic process simulations, and assists in deviation management and inspection readiness, contributing to consistent, compliant, and right-first-time pharmaceutical manufacturing.

Essential Functions:

- Perform IPQA (In-Process Quality Assurance) activities during manufacturing and packing operations

- Oversee calibration of IPQA instruments

- Review of and release of Batch

- Review the in-process and finished product COA before batch release

- Keeping records & review of equipment’s logbooks, dispensing logs, housekeeping records, environmental monitoring records, calibration record, batch records

- Execute Line Clearance and Readiness for manufacturing, packing, and dispensing areas

- Conduct routine In-Process Checks and coordinate with IPQC (In-Process Quality Control)

- 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

- Perform Environmental Monitoring and routine monitoring of manufacturing areas

- Ensure assurance of cleaning,



sterilization, and aseptic manipulations

- Support Sampling of Cleaning Validation and record compilation

- Assist in Process Validation Reports (PVR – Process Validation Report) activities

- Support Aseptic Process Simulation (Media Fill) monitoring

- Ensure Good Documentation Practices (GDP – Valuable Documentation Practices) compliance

Participate in Routine GMP Inspections and quality record reviews

-

Additional Responsibilities:

- Real-time Monitoring and Compliance Reporting.

- Participation in Investigations.

- Provide on-the-job training to shop floor personnel on GMP practices, quality standards, and documentation practices.

- Maintain IPQA-related documents and records in a state of audit readiness.

- To have good written and verbal communication skills in English language.

Education:

- B. Pharm B. Pharm - Required

- M. Pharm M. Pharm - Preferred

Experience:

- 1 year or more in 1 - 4 Years

Specialized Knowledge: Licenses:

Amneal is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, national origin, age, disability, genetic information, protected veteran status, or any other characteristic protected by applicable federal, state, or local laws. If you require a reasonable accommodation to complete the application process or to participate in any part of the hiring process, please contact us at [email protected] . Requests will be handled confidentially and in accordance with applicable laws.

📌 Executive, IPQA (Ahmedabad)
🏢 Amneal Pharmaceuticals
📍 Ahmedabad