Staff Engineer, Advanced Operations (Orthopedic Instruments)

Stryker • Portage, MI

233d

About The Position

Stryker is one of the world's leading medical technology companies and is dedicated to helping healthcare professionals perform their jobs more efficiently while enhancing patient care. Stryker offers a diverse array of innovative medical technologies, including reconstructive, medical and surgical, and neurotechnology and spine products to help people lead more active and more satisfying lives. We are currently seeking a Staff Engineer to join our Orthopedic Instruments Division to be based in Portage, Michigan.

Requirements

• Bachelor's Degree in engineering required.
• 4+ years of related experience required.
• Must be able to read and interpret complex engineering drawings and have a good understanding of geometrical dimensioning and tolerancing.
• Experience in an FDA (Med Device, Med Tech) regulated or regulated industry (Aerospace, Automotive) highly preferred.
• Experience in executing complex problem-solving techniques related to manufacturing/design technical issues highly preferred.
• Good understanding of Design for Manufacturing (DFM), related statistical tools and validation/verification techniques highly preferred.
• Good knowledge of manufacturing processes, materials, product and process design highly preferred.

Responsibilities

• Independently determine and develop approaches to a variety of moderately complex technical problems related to electromechanical assembly.
• 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.
• Select components and equipment based on analysis of specifications, reliability and regulatory requirements.
• Work with quality engineers to develop component specific testing and inspection protocols.
• Lead/support capital acquisition activity from specifying equipment, contract negotiation, installation and validation.
• Analyze 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.
• Ensure adherence to GMP and safety procedures.
• Review and approval of validation documentation.

What This Job Offers

• Career Level: Mid Level
• Industry: Merchant Wholesalers, Durable Goods
• Education Level: Bachelor's degree