Quality Assurance Manager, Global Product Transfers (m/f/d)

Are you interested in working for a global company where you can work across functions and on a wide-variety of projects?

As a member of Stryker's RA / QA team, that is exactly what you will do! Here, we provide our RA / QA team the opportunity to learn new things, as well as endless growth opportunities! If you are interested in working at one of the World’s Best Workplaces, apply now !

Need another reason to apply? Here are 10 reasons to join our Regulatory Affairs / Quality Assurance team :

As a Quality Assurance Manager, Global Product Transfers (m / f / d) at Stryker you will support Global Quality Operations ! In this role, you will report to the Director of Validation and Product Transfer and lead the Global Product Transfer Team.

In this role, you will manage a team within the QA Product Transfer organisation, responsible for quality-related activities as it applies to Product Transfer.

Join us in shaping the future of quality operations at Stryker.

What will you do

As a Quality Assurance Manager, Global Product Transfers (m / f / d) you will be supporting transfers globally, (Supplier to Supplier, Supplier to Stryker, Stryker to Supplier, Stryker to Stryker).

You will provide interpretation and guidance on Regulations, Corporate and Site Local procedures as they relate to quality activities such as FMEA, MSA’s, Validations and Qualifications.

You will be the point of contact for quality for manufacturing transfers at Scoping, Planning and Execution phases.

You will enable successful completion of manufacturing transfer to achieve its quality, cost and time requirements.

You will provide expertise for at least 4 quality specialist associated with manufacturing transfer.

What will you need

You have completed BS in Engineering, Science, or related degree; MS is preferred.

You have gained a minimum of 8 years’ experience in medical technology or another regulated sector in the area of Quality Assurance, Manufacturing or Engineering.

You demonstrate a strong understanding of Manufacturing Transfers.

You have gained a minimum of 2 years’ experience in people management.

You possess strong communication, project management and leadership skills as well as have the ability to manage multiple projects simultaneously and influence in the matrix.

Ideally you have strong understanding of Medical device GMP requirements.

Your English language skills enable you to collaborate with colleagues and stakeholders on a global basis as well in the local office.

German or French or Polish would be an advantage.

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 on site at our locations should be always given to build sustainable relationships and maintain personal contact with colleagues as well as the departments.

Your application

We are looking forward to your online application including CV in English (cover letter, transcript of results, and references are nice to have).

Please note to upload all attachments directly in our application procedure under the item "CV".

Please note that the internal job title may differ from the ad title.

Your contact :

In case you have further questions regarding the position, please feel free to directly reach out to Monika Ambroziak : @

About Stryker Stryker is a global leader in medical technologies and, together with its customers, is driven to make healthcare better.

The company offers innovative products and services in MedSurg, Neurotechnology, Orthopaedics and Spine that help improve patient and healthcare outcomes.

Alongside its customers around the world, Stryker impacts more than 130 million patients annually. More information is available at