Katalyst Healthcares and Life Sciences
Responsibilities:
- Drive process validation activities to ensure compliance with medical device regulations.
- Design and develop equipment and tooling to support production needs.
- Provide hands-on production support to address and resolve manufacturing issues.
- Develop and maintain detailed documentation to support production processes.
- 3+ years of experience in medical device manufacturing.
- Proficiency in process validation and documentation (IQ/OQ/PQ).
- Equipment/tooling design experience is required.
- Experience with either injection molding or laser welding is preferred.