Senior Officer, Quality Control
Amneal Pharmaceuticals · Ahmedabad · onsite · Posted 49d ago
Not disclosed3–6 yrsfulltimeSourced from
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About this role
Description
JOB DESCRIPTION
The position is responsible for in-process and final product quality analyses and inspection in compliance with established specifications, standards, and regulatory requirements. The role involves interpreting and evaluating analytical results for accuracy and precision using approved methods, calibrated instruments, and defined procedures. The role tests random samples of finished goods, audits and monitors manufacturing processes and outputs against internal and regulatory standards, and identifies ongoing quality issues to prevent potential production risks. The position supports accept/reject decisions, reports manufacturing process deviations and defects, maintains robust documentation, and contributes to continuous improvement in product quality and compliance.
Essential Functions
QUALIFICATIONS
JOB DESCRIPTION
The position is responsible for in-process and final product quality analyses and inspection in compliance with established specifications, standards, and regulatory requirements. The role involves interpreting and evaluating analytical results for accuracy and precision using approved methods, calibrated instruments, and defined procedures. The role tests random samples of finished goods, audits and monitors manufacturing processes and outputs against internal and regulatory standards, and identifies ongoing quality issues to prevent potential production risks. The position supports accept/reject decisions, reports manufacturing process deviations and defects, maintains robust documentation, and contributes to continuous improvement in product quality and compliance.
Essential Functions
- Perform In-Process Testing (IPT) and Finished Product (FP) Testing as per approved specifications
- Interpret and evaluate analytical results for accuracy, precision, and compliance
- Execute Sampling and Testing Procedures for RM/PM (Raw Material / Packaging Material)
- Review and approve Certificate of Analysis (COA) Documentation
- Conduct Review of Analytical Data (RM/PM/FG/IP/IV) and ensure data integrity
- Identify quality issues and support Change Control & Deviation Management
- Review and investigate Out-of-Specification (OOS) and OOT (Out of Trend) results
- Ensure compliance with 21 CFR Part 210 & 211 (Code of Federal Regulations – Current Good Manufacturing Practice for Drugs)
- Maintain Good Documentation Practices (GDP) and laboratory records
- Support Internal and External Audits and regulatory inspections
- Use analytical instruments and measuring devices for accept/reject decisions
- Report manufacturing deviations, defects, and improvement recommendations
- To be responsible for Investigation related to LIR, deviations, OOS and OOT.
- To be responsible for Initiation of Deviations, OOS, OOAL, CRN and CAPA's.
- To be responsible for Handling of Caliber e-LIMS
- Activities other than defined in the Job responsibility are to be done as per the requirement of HOD, by following HOD's instruction and guidance.
QUALIFICATIONS
- Bachelors Degree (BA/BS) B. Sc. - Required
- Master Degree (MS/MA) M. Sc. - Preferred
- 3 years or more in 3 - 6 Years
Sourced from foundit
Skills
Change Control Deviation ManagementSampling and Testing Proceduresanalytical instruments
About Amneal Pharmaceuticals
Amneal Pharmaceuticals
Pharma
5.5k+
employees
2002
24 years old
Bridgewater, New Jersey
United States (USA)
About
Amneal Pharmaceuticals operates in the pharmaceutical sector, focusing on developing accessible and affordable medicines to address critical healthcare challenges.
Industries
PharmaBiotechnologyClinical Research
Employee ratings
1,455 reviews
4.2/ 5
Culture
4.0
Career growth
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Work-life
4.2
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