Senior Officer Quality Control

Amneal Pharmaceuticals LLC; Ahmedabad District; Presencial; INR 350 000 - 550 000; Tempo integral

Resumo da oferta

Amneal Pharmaceuticals LLC is seeking a Quality Analyst to conduct in-process and finished product testing, ensuring results meet regulatory specifications. The role emphasizes data integrity, COA review, and deviation management to prevent production risks.

The candidate should have 3+ years of experience in QA or analytical labs within pharmaceutical manufacturing, with a BA/BS and preferably an MS. Compliance with 21 CFR Part 210 & 211 and GDP is essential.

Qualificações

• Bachelor's degree required; Master’s preferred.
• 3+ years in QA testing or analytical labs in pharma/manufacturing.

Responsabilidades

• Perform IPT and FP testing as per specs.
• Interpret results for accuracy and compliance.
• Review RM/PM sampling and testing procedures.

Conhecimentos

In-Process Testing

Finished Product Testing

COA Review

Data Integrity

OOS/OOT Investigation

Deviation Management

Change Control

GDP & Documentation

Regulatory Compliance

Audit Support

Formação académica

Bachelors Degree (BA/BS) / B.Sc.

Master Degree (MS/MA) / M.Sc.

Descrição da oferta de emprego

Job Description:

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

Additional Responsibilities:

• To be responsible for Investigation related to LIR, deviations, OOS and OOT.

• To be responsible for Initiation of Deviations, OOS, OOAL, CRN and CAPAs.

• 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 HODs instruction and guidance.

Qualifications

Education:

• Bachelors Degree (BA/BS) B. Sc. - Required

• Master Degree (MS/MA) M. Sc. - Preferred

Experience:

• 3 years or more in 3 - 6 Years

Specialized Knowledge: Licenses:

Requirements: