- Temporary
- Full Time
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Why join Stryker?
Looking for a place that values your unique talents? Discover Stryker's award-winning culture.
We are proud to offer you our total rewards package which includes bonuses, healthcare, insurance benefits, retirement programs, wellness programs, as well as service and performance awards – not to mention various social and recreational activities, all of which are location specific.
Job description
As a Senior Engineer, Product Transfer (m/f/d) you will oversee the seamless and timely transfer of products across multiple sites, with a strong emphasis on effective communication and coordination between Stryker’s sites. This role focuses on the engineering activities required to move production lines and ensure smooth operational transitions.
This is initially 18 months fixed-term position.
What you will do:
Provide engineering support for product transfers, ensuring all activities are completed and documented in accordance with the latest Stryker procedures.
Define the technical objectives of engineering assignments and make decisions regarding the direction and outcomes of these assignments.
Monitor and control the progress of work, ensuring the sound application of engineering principles and the proper use of policies and procedures.
Analyze equipment to establish operating data, conduct experimental tests, and interpret the results.
Participate in the creation of Validation, PFMEA, Control Plan, SOP, PPAP, and other Stryker internal process qualifications related to product transfers.
What you will need:
Required:
Bachelor’s degree in Engineering, Science, or a related field.
2+ years of engineering experience within production / manufacturing in a highly regulated industry (medical devices, pharma, automotive, aerospace, food & beverage).
Knowledge of process/product validation, statistical methods, and process mapping.
Strong problem-solving skills in manufacturing/design technical issues.
Excellent English and German language skills, enabling seamless collaboration with local and global stakeholders.
Preferred:
Experience in medical device or manufacturing industries, ISO 13485, FDA 21 CFR Part 820, and global quality standards is nice to have.
Diversity is important to us. We welcome applications from people regardless of their ethnic, national or social origin, gender, disability, age or sexual identity.
Additional information
Thanks to our flexible working hours model, you will have the opportunity to work partially from the home office. However, a regular presence of minimum 1 day a week on site in Tuttlingen should be always given to build sustainable relationships and maintain personal contact with colleagues as well as the departments.
Please note that the internal job title may differ from the ad title.