Beschreibung
RESPONSIBILITIES• Establish and maintain master validation plans for in-house production, including, control plans, gauge R&R, test method validations, process flows, maintenance and qualification routines.
• Collaborate with the external manufacturing partners in validating the supply chain.
• Grow with the organization to enable Design Transfer to commercial-stage operational processes and provide continued engineering leadership in scale-up phase.
YOUR PROFILE
• 10 years medical device engineering / manufacturing experience.
• Strong technical understanding of validation of manufacturing processes. Experience with statistical methods is highly desirable.
• Prior experience in medical device assembly including cleaning, silicone molding, and interconnect technologies, is considered an advantage.
• MSc or BSc degree in engineering.
Please forward your updated CV to