Job Description:

We are seeking a detail-oriented Quality Engineer with experience in the pharmaceutical industry to support quality engineering activities across manufacturing and laboratory operations. The ideal candidate will have hands-on experience with deviations, CAPA, change control, validation, and GMP compliance.

Responsibilities :

• Support quality engineering activities for manufacturing and lab operations, including deviation investigations, CAPA, change control, and validation.


• Review batch records, SOPs, technical documents, and quality reports to ensure compliance with GMP, cGMP, and GLP standards.


• Assist in method development support, qualification activities, and validation documentation review for processes, equipment, and laboratory systems.


• Collaborate with QA, QC, Manufacturing, Validation, and Engineering teams to re...