Who We Want​

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Challengers.  People who seek out the hard projects and work to find just the right solutions.​

Teammates.  Partners who listen to ideas, share thoughts and work together to move the business forward.​

Charismatic networkers.  Relationship-savvy people who intentionally make connections with both internal partners and external contacts.​

Strategic thinkers.  Interns who propose innovative ideas and consistently exceed their performance objectives.​

Customer-oriented achievers.  Individuals with an unparalleled work ethic and customer-focused attitude who bring value to their partnerships.​

Game changers.  Persistent interns who will stop at nothing to live out Stryker’s mission to make healthcare better. ​

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What You Get Out of the Internship​

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Stryker, a global leader in medical technology takes great pride in their people, and that’s why we’re looking to expand our talent. As a result, we are looking for the best and brightest students to strengthen our team and drive our business going forward.   Stryker Engineering interns will get to:​

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• Impact the development and manufacturing of cutting edge products​
• Gain experience within a fast paced and growing industry​

• Apply classroom knowledge in a fast-paced and growing industry setting​

• Implement new ideas, be constantly challenged, and develop your skills​​​

Description

Identify and prepare environmental data to comply with international, federal, state, and local product environmental regulations, customer expectations, and company policies. Major areas of emphasis are data pertaining to EU directives and regulations such as EU RoHS, EU REACH, EU PPWR, U.S. Proposition 65, EU POPs, and EU-MDR.

Stryker, a global leader in medical technology takes great pride in their people, and that’s why we’re looking to expand our talent. As a result, we are looking for the best and brightest students to strengthen our team and drive our business going forward.

Stryker Regulatory Engineering Interns Will Get To:

• Learn about regulations within the medical device industry.
• Implement new ideas, be constantly challenged, and develop your skills
• Network with key/high level stakeholders and leaders of the business
• Be a part of an innovative team and culture.
• Work cross functionally with different departments including R&D Engineering,
• Supplier Quality, Marketing, and Clinical Affairs to assist in regulatory decision
• making and develop a broad understanding of the medical device industry.

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What You Need​

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• Currently working on completion of a Bachelor’s or Master’s degree in related field or equivalent; we will only consider students who plan be enrolled in a degree-seeking program after the summer​

• Cumulative 3.0 GPA or above; must be the case at the date of hire and also will be verified during background check in the spring​

• Must be legally authorized to work in the U.S. and not require employment-based sponsorship now or in the future.​

• Excellent written and verbal communication skills​

• Strong organizational, problem-solving, and analytical skills; able to manage priorities and workflow​

• Versatility, flexibility, and a willingness to work within constantly changing priorities with enthusiasm​

• Ability to exercise independent judgment​

• Proficient on basic computer programs: Microsoft Excel, Word, PowerPoint​

• Proven leadership and business acumen skills​

• Proven ability to handle multiple projects and meet deadlines​

• Strong interpersonal skills​​

$22 hourly wage – $33 hourly wage and either paid corporate housing or a living stipend, dependent upon hiring location.