• Execute engineering tasks for product transfers or new product/process introductions, ensuring adherence to Stryker procedures and complete documentation.

• Maintain the quality of processes and products as per operation and material specifications specific to the project.

• Support the selection of components and equipment through evaluation of specifications, reliability, safety, and relevant regulatory requirements.

• Contribute to capital acquisition activities, including specifying, installing, and validating equipment within project parameters.

• Perform equipment analyses, conduct tests, and review results, participating in process review meetings.

• Create PFMEA, Control Plans, Work Instructions, and related manufacturing documents for the project.

• Develop PPAP and perform process capability studies for product transfers and launches.

• Ensure GMP, safety compliance, conduct MSA studies, train manufacturing staff, and interact with global teams to meet project goals.

Required

• Bachelor’s degree in an engineering discipline

• Minimum 4 years of experience as Engineer on new product introduction or product transfer roles

• Experience in an FDA regulated or highly regulated industry

• Experience with process validation

• Advanced level of English

• Availability to work under a 12-month contract

Preferred

• Six Sigma Yellow belt or higher certification

• Experience in the Medical Devices industry