A global leader in the Medical Device field has an opening for a Senior Quality Engineer to join their team. The Senior Quality Engineer is involved with all aspects of the manufacturing operation form assessing equipment needs to ongoing validation of equipment and processes.
Responsibilities:
- Author and execute validation protocols
- Contribute to development of process designs and validation protocols
- Assist in exception report root cause analysis, and resolution of QA and Validation projects
- Provide QA input to the maintenance of the Validation Master Plan
Qualifications:
- 4+ years of experience in Medical Device or Pharmaceutical industry
- Able to work and influence cross functional teams
- 2+ years authoring validation protocols
If you are interested in learning more about this excellent opportunity apply today!