Work Flexibility: Hybrid

Sr. Engineer – Product Transfer

As a team, we are responsible for the manufacturing process development for products that are transferred between Stryker plants or suppliers. As the main contact for the site, we form a strong virtual team with Stryker development divisions and suppliers worldwide. We coordinate the projects internationally and combine different divisional and cultural requirements into a successful strategy.

What will you do

• As part of product transfers of a product line that is being relocated from one site to another, you will actively shape the process development and ensuring that all activities are completed and documented in accordance with the Stryker procedures.
• In addition to coordinating internal and external partners, you are responsible for solving technical challenges and implementing efficient manufacturing and testing strategies in a highly technical environment.
• You will make a significant contribution to the realization of short transfer times, considering innovative problem-solving methods, continuous development and optimization of our manufacturing processes.
• As a process engineer, you work closely with cross functional teams and international project teams and process experts.
• Participate in PFMEA, Control Plan, SOP and PPAP generation associated with product transfers. 
• Complete capability and MSA studies for in process inspection and generate subsequent Inspection documentation.

What will you need

• Master's or bachelor's degree in engineering (automation technology, process engineering, electrical engineering, mechanical engineering, medical technology, industrial engineering or similar) with 6 to 8 years of professional experience in the field of process development and/or process optimization.
• Hands on experience with Medical Device Post Market Surveillance.
• Experience with Product development/ Transfer, Process Engineering, Supplier development /PPAP.
• Excellent Interpersonal and analytical Skills.
• Good knowledge of manufacturing processes, materials, product and process design. 
• Must be able to read and interpret complex engineering drawings and have the ability to understand geometrical dimensioning and tolerancing. 
• Experience in an FDA regulated or regulated industry beneficial. 
• Individual is willing to travel occasionally for business purposes

Travel Percentage: 10%