Stryker

Stryker

Staff Engineer, Product Transfer

Company

Stryker

Role

Staff Engineer, Product Transfer

Location

Poland

Job type

Full time

Posted

2 days ago

Salary

Not disclosed by employer

Job description

Work Flexibility: Hybrid

Shape the future of medical technology in Skawina

At Stryker, we don’t just build products—we improve lives. As a Staff Engineer, you’ll play a key role in bringing innovative medical technologies to market faster, safer, and more efficiently. This is a high-impact role where your expertise will directly influence cutting-edge manufacturing processes and product launches.

What will you do:

  • Lead and support new product introductions, transfers, and process implementations—ensuring smooth, compliant, and efficient execution aligned with global standards.

  • Optimize performance and quality using advanced engineering and statistical techniques to enhance product quality, reduce variability, and accelerate time-to-market—without compromising compliance or cost.

  • Own critical engineering decisions by selecting components, defining equipment requirements, and contributing to capital investments—from specification through validation and deployment.

  • Lead validation & process excellence: take ownership of validation strategies, including IQ/OQ/PQ, MSA, and capability studies. Drive PFMEA, Control Plans, and PPAP activities to ensure robust and scalable processes.

  • Collaborate & influence while partnering cross-functionally with Quality, R&D, and Manufacturing teams. Share your expertise, mentor others, and help elevate engineering standards across the organization.

  • Analyze process data, lead experiments, and drive continuous improvement initiatives using sound engineering judgment and modern tools.

What do you need:

  • Degree in Mechanical Engineering or related engineering discipline

  • Proven experience solving complex manufacturing challenges while working in a team based environment - minimum 4 years

  • Experience of MES/SAP, GD&T, Process mapping, statistical methods and process/ product validations and verification techniques.

  • Experience in an FDA regulated or regulated industry beneficial.

  • Excellent analytical skills, ability to plan, organise and implement concurrent tasks.

  • Ability to communicate ideas clearly and influence across teams in a collaborative, fast-paced environment

Travel Percentage: 20%

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