For Candidates → For Companies →

Back to all jobs

QA Officer

Pharmaceuticals Punjab 2 yrs exp

Job Description

Key Responsibilities

- Prepare, review, issue and control QA documents according to cGMP requirements.

- Review Batch Manufacturing Records (BMR), Batch Packing Records (BPR), logbooks and other production documents.

- Prepare and revise SOPs, formats, specifications and protocols.

- Handle deviations, CAPA, change controls, incidents and investigations.

- Maintain document-control activities, including issuance, retrieval, archival and version control.

- Conduct routine shop-floor monitoring and ensure compliance with approved procedures.

- Support line clearance and in-process checks during API manufacturing operations.

- Ensure compliance with cGMP, data-integrity requirements and ALCOA+ principles.

- Assist with internal, customer and regulatory audits.

- Coordinate with Production, QC, Engineering and Warehouse teams for QA-related activities.

- Maintain training records and support cGMP and SOP training.

- Ensure all records are complete, accurate and maintained according to regulatory requirements.

Candidate Profile

- Must have 2–3 years of QA experience in an API manufacturing company.

- Good knowledge of cGMP documentation and pharmaceutical quality systems.

- Familiarity with SOPs, BMR/BPR review, deviations, CAPA and change controls.

- Good written communication, documentation and coordination skills.

Minimum QualificationB.Pharm / M.Pharm / B.Sc. / M.Sc

Experience Level (Years)2 - 3

LocationPunjab

Area of WorkQA

Salary Range (In LPA) -

Apply Now