Work Flexibility: Onsite
**What you will do-**:
- 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 general teams to meet project goals.
**What you need-**:
**Required**
- Bachelor's degree in an engineering discipline.
- Minimum of 4 years of experience as Sr. Engineer on new product introduction or product transfer roles.
- Experience in an FDA regulated or highly regulated industry.
- Advanced level of English.
**Preferred**
- Six Sigma Yellow belt or higher certification.
- Experience in the Medical Devices industry.
Travel Percentage: 10%