Working at IPG Photonics you can expect challenging projects, a motivating and friendly environment, and competitive benefits.
Job Function
- Conduct product design control activities for new and sustaining product development efforts
- Support risk analysis activities, including design and process FMEA
- Support Process/Design Validation/Verification activities, including software validation and IQ/OQ/PQ activities
- Support Design Engineering in the creation of Design History and Technical Files
- Interact with third-party test houses that conduct compliance testing of IPG products
- Assist regulatory department with FDA, CE, and other regulatory submissions
- Perform all other essential duties as assigned
- Bachelor's Degree in scientific or engineering field; electrical engineering is preferred
- 3-5 years of experience with engineering and development of Class II electro-mechanical medical devices
- Knowledge of Design Controls and Risk Management practices, regulations and standards, such as FDA QSR's, ISO 13485, ISO 14971, IEC 60601, 60825, 62366, and 62304 is preferred
- Supporting medical device compliance testing (e.g. EMC, EMI, IEC) with external test houses, such as TUV an Intertek
- Maintenance of technical design documentation, such as design specifications, verification/validation protocols, and DFMEA/PFMEA.
- Working knowledge of advanced statistical methods (e.g., hypothesis testing, DOE, ANOVA, R&R studies, capability, tolerance interval analysis, power and sample size determinations, etc.), including statistical software tools, such as Minitab, is preferred
- Experience with lasers and optical technologies desired, but not necessary
- Strong working knowledge of Microsoft Word and Excel
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