Intern Regulatory International Registration (f/m)

Allgemeines

Your key responsibilities
• As a member of the regulatory affairs team you support the international regis- tration of medical devices and develop a broad understanding of regulation within the industry.
• You assist local and international colleagues with how devices can be approved for market distribution.
• Furthermore, you perform in-depth review of regulatory data/information.
• You prepare registration support packages for registering products globally to
ensure that Stryker products can reach our clients around the world.
• You assist in notarization legalization and in the apostille of documents.
• You build the interface between regulatory and cross functional teams to
address questions from regulatory authorities.
• As an intern at Stryker you have the unique opportunity to gain experience in
the regulation of medical devices to ensure safety and efficacy is delivered with every product.

What we are looking for?
• You are currently enrolled in a scientific or project management field of study.
• Furthermore, you are highly proficient on MS-Office programs and in Excel.
• You are detail oriented and you can communicate key ideas verbally and in
writing clearly.
• You work well in a team-oriented, cross-functional environment and you are
highly proficient in English and German.
• You can handle multiple tasks and operate in a fast-paced environment.
• In addition, you are assertive, take initiative, self-starter, energetic, motivated
and self-managed.