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Summer 2025 Intern - Regulatory Affairs - California

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Stryker

11d ago

  • Internship
    Full-time
    Summer Internship
  • Science
  • San Jose

AI generated summary

  • You must be pursuing a relevant degree with a 3.0 GPA, authorized to work in the U.S., possess strong communication skills, and be proficient in Microsoft Office.
  • You will collaborate across departments, conduct regulatory intelligence, prepare submissions, shadow specialists, support post-market reporting, and develop regulatory assessments for product changes.

Requirements

  • Currently working on completion of a Bachelor’s or Master’s degree in related field or equivalent; we will only consider students who plan to 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 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 interpersonal skills.
  • Ability to exercise independent judgment and proven leadership and business acumen skills.
  • Proven ability to handle multiple projects and meet deadlines.
  • Versatility, flexibility, and a willingness to work within constantly changing priorities with enthusiasm.
  • Strong organizational, problem-solving, and analytical skills; able to manage priorities and workflow.
  • Proficient on basic computer programs: Microsoft Excel, Word, PowerPoint.

Responsibilities

  • - 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.
  • - Perform Regulatory Intelligence activities to ensure divisional regulatory strategy remains optimally efficient amidst changing regulations and increasing liability.
  • - Prepare various regulatory submissions for registering products globally to ensure Stryker products can reach our patients around the world.
  • - Shadow RA Specialists at new product development meetings to gain exposure to the collaborative design and development process associated with bringing a new product to market.
  • - Support the Post Market Regulatory Reporting team on projects and initiatives that allow the organization to monitor the performance of devices that have been released to market and detect any potential safety and/or product quality issues.
  • - Help develop robust Regulatory assessments and strategy for proposed change notifications in different regions to ensure minimal disruption to registrations or approvals.

FAQs

What is the duration of the internship?

The internship is for the Summer of 2025.

What majors are preferred for this internship?

A scientific or technical discipline is preferred for this internship.

What is the hourly wage for this internship?

The hourly wage ranges from a minimum of $19 to a maximum of $33, and interns may receive either paid corporate housing or a living stipend, depending on the hiring location.

What kind of experience will I gain as an intern at Stryker?

You will gain experience in regulatory affairs, network with high-level stakeholders, apply classroom knowledge in a practical setting, and learn about regulations within the medical device industry.

Are there any GPA requirements for this internship?

Yes, applicants must have a cumulative GPA of 3.0 or above, which will be verified during the background check.

Is sponsorship available for international students?

No, applicants must be legally authorized to work in the U.S. and cannot require employment-based sponsorship now or in the future.

What skills are necessary to succeed in this role?

Strong written and verbal communication skills, interpersonal skills, leadership and business acumen, organizational, problem-solving, and analytical skills are necessary for this role.

Will interns have the opportunity to engage with different departments?

Yes, interns will work cross-functionally with various departments, including R&D Engineering, Supplier Quality, Marketing, and Clinical Affairs.

What kind of projects can interns expect to work on?

Interns will perform Regulatory Intelligence activities, prepare regulatory submissions, support Post Market Regulatory Reporting, and assist in the development of regulatory strategies.

What is the work environment like at Stryker?

Stryker fosters an innovative team culture that values collaboration, creativity, and a commitment to making healthcare better.

Stryker

Together with our customers, we are driven to make healthcare better. #WeAreStryker

Manufacturing & Electronics
Industry
10,001+
Employees
1941
Founded Year

Mission & Purpose

Stryker is one of the world’s leading medical technology companies and, together with its customers, is driven to make healthcare better. The company offers innovative products and services in Medical and Surgical, 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 stryker.com and careers.stryker.com. PRODUCTS: ● Reconstructive ● MedSurg ● Neurotechnology & Spine FACTS: ● 2022 Sales: $18.4 billion ● Industry : Medical Instruments & Supplies ● Employees: 51,000+ globally ● 40 Years of Sales Growth leading up to 2020 ● 44+ Manufacturing and R&D Locations Worldwide ● $1.45 billion spend on research and development in 2022 ● 12,000+ patents owned globally in 2022 ● Products Sold in Over 75 Countries ● Fortune 500 Company ● 6 consecutive years as one of Fortune's World's Best Workplaces