(Senior) Process Engineer (m/f/d) Manufacturing (24 Months)
Full-timeSeniorBachelors
Description
Work Flexibility: Hybrid<p style="text-align:inherit"></p><p style="text-align:inherit"></p><p>As a (<b>Senior) Process Engineer (m/f/d)</b> you will oversee the seamless and timely transfer of products across multiple sites, with a strong emphasis on effective communication and coordination between Stryker’s sites. This role focuses on the engineering activities required to move production lines and ensure smooth operational transitions.</p><p></p><p>This is initially <b>24</b><b><b> </b>months</b> fixed-term position.</p><p></p><p><b>What you will do: </b></p><ul><li><p>Provide engineering support for product transfers, ensuring all activities are completed and documented in accordance with the latest Stryker procedures.</p></li><li><p>Define the technical objectives of engineering assignments and make decisions regarding the direction and outcomes of these assignments.</p></li><li><p>Monitor and control the progress of work, ensuring the sound application of engineering principles and the proper use of policies and procedures.</p></li><li><p>Analyze equipment to establish operating data, conduct experimental tests, and interpret the results.</p></li><li><p>Participate in the creation of Validation, PFMEA, Control Plan, SOP, PPAP, and other Stryker internal process qualifications related to product transfers.</p></li></ul><p></p><p><b>What you will need: </b></p><p>Required:</p><ul><li><p>Bachelor’s degree in Engineering, Science, or a related field.</p></li><li><p>2+ years of engineering experience within production / manufacturing in a highly regulated industry (medical devices, pharma, automotive, aerospace, food & beverage).</p></li><li><p>Knowledge of process/product validation, statistical methods, and process mapping.</p></li><li><p>Strong problem-solving skills in manufacturing/design technical issues.</p></li><li><p>Excellent English and German language skills, enabling seamless collaboration with local and global stakeholders.</p></li></ul><p></p><p>Preferred:</p><ul><li><p>Experience in medical device or manufacturing industries, ISO 13485, FDA 21 CFR Part 820, and global quality standards is nice to have.</p></li></ul><p></p><p><i>We have signed the Diversity Charter and are proud to be part of this initiative to promote diversity in the workplace. Because diversity is important to us!<br />We welcome applications from people regardless of their ethnic, national, or social background, gender, disability, age, or sexual identity.</i></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p>Travel Percentage: None<p style="text-align:inherit"></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p></p><p></p><p></p><p></p>