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Executive, Quality Control at Amneal Pharmaceuticals — Ahmedabad

Experience4–5 yrs
SalaryNot disclosed
Work modeonsite
Posted26 Sept 2026

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About Amneal Pharmaceuticals

Amneal Pharmaceuticals is hiring in Ahmedabad in pharma biotech. This role looks for around 4+ years of experience.

Skills

pharmacopeial standards
Good Documentation Practices
current Good Manufacturing Practice
Good Laboratory Practice
Laboratory Information Management Systems
laboratory instrument calibration
method validation
corrective and preventive actions

The role

A quality control executive at a pharmaceutical manufacturing company performs pharmaceutical analysis using pharmacopeial standards and manages Good Manufacturing Practice compliance, with expertise in laboratory instruments and Laboratory Information Management Systems. The role supports injectable product release through method validation and corrective and preventive actions.

Full job description

Description

JOB DESCRIPTION

To perform qualitative and quantitative analysis of raw materials and packaging materials In-process and Finished product as per applicable pharmacopeial standards, regulatory requirements, and internal specifications. Ensure timely release and compliance of materials to support uninterrupted manufacturing operations of injectable products.

Essential Functions

Perform testing of raw materials (APIs, excipients) and primary/secondary packaging materials as per approved specifications, SOPs, and pharmacopeial methods (USP, EP, IP, JP, etc.).Ensure accurate and timely recording of results in logbooks, worksheets, and LIMS as per Good Documentation Practices (GDP).Adhere to cGMP, GLP, and safety protocols during sample handling, testing, and equipment usage.Performing qualification, periodic calibration, and maintenance of laboratory instruments.Maintain proper cleanliness, calibration, and qualification status of analytical instruments.Coordinate with warehouse and QA for sampling of incoming materials as per SOPs.Ensure proper labeling, storage, and disposal of samples and reference standards.Support internal, customer, and regulatory audits by providing required documentation and clarifications.Implement corrective and preventive actions (CAPA) as per audit observations.

Additional Responsibilities

Participate in method validation, verification, and transfer activities as required.Assist in updating and reviewing SOPs, specifications, and analytical procedures.Contribute to continuous improvement initiatives in the QC department.Report any out-of-specification (OOS) or out-of-trend (OOT) results promptly to the supervisor.Support cross-functional departments such as QA, Production, and Regulatory Affairs as needed.

Education

QUALIFICATIONS

Bachelors Degree (BA/BS) B. Pharma - RequiredMaster Degree (MS/MA) M. Sc - PreferredMaster Degree (MS/MA) M. Pharma - Preferred

Experience

4 years or more in 4 - 6 Years

Specialized Knowledge: Licenses: