Job Description
```html Work Flexibility: Hybrid Position Summary: Are you an experienced Process Development Engineer with a passion for innovation and a knack for solving complex technical problems? Join our rapidly growing additive NPI team at Stryker, Anngrove, and play a pivotal role in launching cutting-edge joint replacement products. Who We Want: Analytical Problem Solvers: You go beyond fixing issues to identify root causes, evaluate optimal solutions, and propose changes to prevent future problems. Effective Communicators: You can interpret information clearly and accurately, concisely communicating results and recommendations to stakeholders, senior management, and teams. Dedicated Achievers: You thrive in a fast-paced environment and are committed to ensuring projects are completed to meet regulations and expectations. Collaborative Partners: You build and leverage cross-functional relationships to bring together ideas, information, use cases, and industry analyses to develop best practices. What you will do: Provide engineering support for new product and process introductions, ensuring that all activities are completed and documented in accordance with the Stryker new product development procedures. Ensure quality of process and product as defined in the appropriate operation and material specifications. Will assist in the selection of components and equipment based on analysis of specifications, reliability and regulatory requirements. Work with quality engineers to develop component specific testing and inspection protocols. Support capital acquisition activity from specifying equipment, contract negotiation, installation and validation. Will analyse equipment to establish operating data, conduct experimental test and result analysis. Lead and/or participate in process review meetings. Participate in PFMEA, Control Plan, SOP and PPAP generation associated with product transfers and launches. Complete capability studies for in process inspection and generate subsequent inspection documentation. Conduct MSA studies for new products and new processes. Provide training for manufacturing team members. Ensure adherence to GMP and safety procedures. Review and approval of validation documentation. What you will need: B.S in Mechanical Engineering or related engineering discipline with up to 2 years’ experience. Self-starter with demonstrated efficient work methods, analytical & problem solving skills, and ability to handle multiple tasks in a fast-paced environment. The individual should enjoy working in a fast-paced, dynamic and results-oriented team environment. Excellent Interpersonal Skills - able to express ideas and collaborate effectively with multidisciplinary teams. Excellent analytical skills, ability to plan, organise and implement concurrent tasks. 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. Why Join Us? This permanent opportunity offers a fantastic scope for career progression and development within a dynamic and innovative environment. If you have strong experience in process development and a passion for continuous learning, this could be the perfect role for you! Apply now to become part of a team that's shaping the future of joint replacement products through advanced additive manufacturing. Travel Percentage: None ``` #J-18808-Ljbffr