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We are seeking a highly skilled Manufacturing Engineer to join our team at Sonova. As a key member of our production team, you will be responsible for supporting production activities in the medical device industry, including yield improvement initiatives, product disposition, continuous improvement activities, assembly procedure development, and process validations.
Key Responsibilities- Participate and execute validation strategy.
- Create, write and execute process validations.
- Lead Projects with some supervision.
- Support and lead continuous improvement activities and yield improvement initiatives.
- Develop, update pFMEA.
- Support production on non-conformances, determine root cause and develop solutions.
- Write technical reports.
- Bachelor's Degree in appropriate engineering field of study or equivalent work experience.
- English Spoken 80% Written 80%.
- 2-5 years' experience as a manufacturing or mechanical engineering in the medical device industry.
- Proven ability to work creatively and analytically in a problem-solving environment demonstrating teamwork, innovation and excellence.
- Self-motivated, decisive, with the ability to adapt to change and competing demands.
- Flexible with proven ability to conform to shifting priorities, demands and timelines through analytical and problem-solving capabilities.
- Strong verbal and written communication skills.
- Strong ability to collaborate in teams and directly with other.
- Strong interpersonal skills.
- Strong experience with process validation - IQ, OQ, PQ.
- Familiarity with processes such as FMEA, CAPA and Standard Works.
- Good overall theoretical knowledge of mechanical engineering.
- Proficient in Microsoft office, Word, Excel, PPP, Outlook & PLM.
- Experience with CAD.
Sonova is a leading provider of solutions for hearing care and medical devices. We are committed to delivering high-quality products and services that improve the lives of our customers.
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