Process Development Engineer Medical Devices (m/f/d)
About Heraeus
Making displays foldable? Helping hearts beat with medical innovations? Or breathing new life into precious metals? As a family-owned global technology group we help our customers to always being one step ahead.
About Heraeus Medevio
Together we improve lives. At Heraeus Medevio, we bring lifesaving and life-changing medical devices to market through partnerships with medical device manufacturing companies. Backed by Heraeus Group, we are committed to the growth of our teams and organization by providing an open space for open minds.
To reach our vision of improving 100 million lives every year, we foster a culture of curiosity that thrives on challenge, continuous learning, growth, and the opportunity to try new things. With sites in the United States, European Union, and Asia, and over 2,200 employees worldwide, together, we will meet tomorrow's challenges today.
The following challenges await you:
- Within our international engineering team, you will be responsible for the development and optimization of manufacturing processes for existing, as well as novel products, working closely with the relevant product realization teams.
- You will carry out and document process characterizations and process validations independently.
- You have a passion for the quality of the products you are responsible for and support processes throughout the lifecycle of the products.
- You analyze quality factors based on statistical parameters.
- You support the specification and implementation of new technologies in the company as part of the process engineering team.
- You will accompany the transfer of new products from development status to serial manufacturing between development and operations sites.
Your profile:
- You successfully completed a vocational training or an engineering degree and obtained professional experience in the field of plastics and process engineering, catheter manufacturing technologies or plastics processing in serial manufacturing environments.
- Relevant professional experience in the field of medical technology or in a similarly regulated environment desirable.
- Good understanding of process development, process validation and statistics.
- Experience with product ramp-ups and transfer programs.
- Solid experience in maintaining serial production lines (root cause analysis, quality investigations).
- You are a committed, flexible and motivated team player.
- Communication in German and English (verbally as well as in writing) round up your profile.
- The use of standard IT tools and change control systems is natural for you.
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