Specialist QA
Summary
QA Specialist performing compliance oversight, documentation review, and validation activities in collaboration with Manufacturing, Engineering, and Operations teams at a pharmaceutical/medical device manufacturing site.
We are seeking a Quality Assurance Specialist to perform critical QA oversight activities, ensuring compliance with regulatory requirements, internal quality standards, and site procedures. This role requires the ability to work with minimal supervision while collaborating cross-functionally with Manufacturing, Engineering, Facilities, Validation, and Operations teams
Requirements
- Masters + 2 years of directly related experience; or Bachelors + 4 years of directly related experience
- Change Control, Documentation Review, Validation, PPQ
- Fully Bilingual (English & Spanish)