QA Officer

Key Responsibilities:

QMS Implementation and Oversight:

Maintaining and improving the QMS, including deviation management, change control, CAPA (Corrective and Preventive Actions), and quality reviews.

Deviation and CAPA Management:

Investigating manufacturing deviations, conducting root cause analysis, and ensuring timely and effective CAPA implementation.

Change Control and Document Control:

Managing changes in equipment, facility, process, and documents, and ensuring proper documentation practices.

Audit Readiness and Regulatory Compliance:

Preparing for and participating in audits (internal, regulatory, and third-party), and ensuring compliance with GMP and other relevant regulations.

Training and Quality Culture:

Conducting GMP training programs and fostering a quality-focused culture within the plant.

IPQA Activities:

Conducting in-process quality assurance checks during the manufacturing process, including line clearance, sampling, and verifying adherence to procedures.

Product Release:

Ensuring that products meet quality standards before release.

Industries:Pharmaceuticals

Function: Others