Senior Process Development Engineer – MedTech Innovation

Stryker; Portage (MI); On-site; USD 78,000 - 130,000; Full time

Benefits offered by this job

Health insurance

Dental insurance

Vision insurance

HSA

FSAs

401(k) plan

ESPP

Life insurance

Short-term disability

Wellbeing program

Tobacco cessation program

Job summary

Stryker in Portage, MI is seeking a Senior Engineer, Process Development to join its OrthoTech Division. This onsite role focuses on supporting new product introductions, process development, and capital equipment projects to ensure compliant, efficient manufacturing.

You will analyze processes, perform capability studies, PFMEA, control plans, and validation documentation, while training teams and upholding GMP and safety standards.

Qualifications

• Bachelor’s degree in engineering required.
• 2+ years of applicable full-time work experience required.
• Working knowledge of PFMEA required.
• Ability to read and interpret engineering drawings and GD&T.
• CAD experience required.

Responsibilities

• Provide engineering support for new product and process introductions per NPD procedures.
• Ensure process and product quality per specifications.
• Lead equipment selection and capital acquisitions, installation and validation.
• Analyze equipment data, conduct experiments, and generate results.
• Participate in PFMEA, Control Plan, SOP, and PPAP for transfers and launches.
• Complete capability studies and generate inspection documentation.
• Conduct MSA studies for new products and processes.
• Provide training to manufacturing teams and ensure GMP compliance.

Skills

Analytical skills

Planning & organization

Concurrent task management

Reading engineering drawings

GD&T understanding

Education

Bachelor’s degree in engineering

Tools

CAD

Job description

Stryker in Portage, MI is seeking a Senior Engineer, Process Development to join its OrthoTech Division. This onsite role focuses on supporting new product introductions, process development, and capital equipment projects to ensure compliant, efficient manufacturing.

You will analyze processes, perform capability studies, PFMEA, control plans, and validation documentation, while training teams and upholding GMP and safety standards.