Senior Regulatory Affairs Specialist

2 weeks ago

Portage, United States Stryker Full time

Work Flexibility: Hybrid

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 www.stryker.com

We are currently seeking a Senior Regulatory Affairs Specialist to join our Medical Division to be based Hybrid in Portage, Michigan.

Who we want

  • Self-directed initiators. People who take ownership of their work and need no prompting to drive productivity, change, and outcomes.
  • Strategic thinkers. People who enjoy analyzing data or trends for the purposes of planning, forecasting, advising, budgeting, reporting, or sales opportunities.
  • Collaborative partners. People who build and leverage cross-functional relationships to bring together ideas, data and insights to drive continuous improvement in functions.
  • Dedicated achievers. People who thrive in a fast-paced environment and will stop at nothing to ensure a project is complete and meets regulations and expectations.
  • Goal-oriented developers. Keeping the customer and requirements squarely in focus, people who deliver safe and robust solutions.
What you will do

As the Senior Regulatory Affairs Specialist, you will support Stryker's Emergency Care portfolio for our global market. You will be responsible for maintaining global market access by analyzing the impact of device modifications and emerging regulatory intelligence. You will help identify global regulatory requirements to support new product development. You will enable global product sales in new markets by liaising with global Stryker teams to execute registrations in accordance with health authority requirements.
  • Evaluate device modifications and takes appropriate action to ensure global product compliance.
  • Support new product development in submitting registrations and subsequently support registration renewals in global markets.
  • Analyze and advise on the impact of emerging regulatory intelligence.
  • Provide regulatory input and technical guidance on global regulatory requirements to product development teams.
  • Determine requirements and options for global regulatory submissions, approval pathways, and compliance activities.
  • Prepare and submits regulatory submissions according to applicable regulatory requirements and guidelines in global markets.
  • Participate in preparation and execution of audit required to enable of maintain market access.
  • Identify the need for new regulatory procedures, SOPs, and participates in development and implementation.
What you need
  • Bachelor's Degree (B.S. or B.A.) required; preferably in Science, Engineering or equivalent focus
  • 2 - 4 years of experience in an FDA or highly regulated industry required.
  • 1 - 2 years of experience in a Regulatory Affairs role preferred.
  • Time management skills, writing, coordination, and execution of basic regulatory items
  • Coordinate and support technical and scientific regulatory activities


Travel Percentage: 10%

Stryker Corporation is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, or protected veteran status. Stryker is an EO employer - M/F/Veteran/Disability.

Stryker Corporation will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant. However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, or (c) consistent with the contractor's legal duty to furnish information.

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