About the job
Core
Operating GMP quality systems, managing quality documents, reviewing manufacturing/testing records, and handling deviations, change controls, CAPA, validation, and qualification activities.
Role type
Quality Assurance (QA) Engineer
Builds
Pharmaceutical or medical device products under GMP compliance
Domain
Healthcare / Pharmaceutical Manufacturing
Required skills
GMP compliance, quality system operation, document management, deviation management, change control, CAPA, validation, qualification, regulatory audit/inspection support
Preferred skills
None stated
Technologies
None stated
Responsibilities
Operating GMP quality systems, managing quality documents, reviewing manufacturing/testing records, handling deviations/change controls/CAPA, supporting validation/qualification, assisting with regulatory audits/inspections
Seniority
Entry-level (Bachelor's degree required)
