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Stryker

Senior Director, Regulatory Affairs

Reposted Yesterday
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In-Office or Remote
5 Locations
172K-379K Annually
Expert/Leader
In-Office or Remote
5 Locations
172K-379K Annually
Expert/Leader
The Senior Director of Regulatory Affairs leads strategy and execution for regulatory compliance in the Endoscopy business unit, ensuring alignment with quality and regulatory standards across products.
The summary above was generated by AI
Work Flexibility: Remote or Hybrid or Onsite

The Senior Director, Regulatory Affairs is a key strategist, responsible for developing regulatory strategy for the Endoscopy business unit and delivering Stryker’s best-in-class visualization and connectivity products to market in the United States, Canada and Europe. Through close partnership with business unit leadership, Marketing, R&D, Clinical and Quality teams, the Senior Director and team will develop and advise on product positioning, product entry and exit strategies, among others.

Key Areas of Responsibility:

  • Ensure divisional achievement of quality, regulatory, and compliance targets
  • Direct activities to ensure new product development and product sustainment meet regulatory requirements
  • Develop, lead, and execute a regulatory strategy ensuring that it is appropriate and effective in meeting the business needs
  • Responsible for the selection, supervision, development and objective-setting for team members
  • Develop best practices to ensure compliance and drive revenue through improved customer experience
  • Provide a platform for process improvement
  • May serve as alternate Management Representative
  • Define targets, KPIs, performance objectives, etc. for individuals within functional role, and manage direct reports to meet or exceed these targets
  • Recruit, select, and on-board top talent
  • Develop talent within team to increase performance
  • Actively address performance issues on team
  • Maintain a high level of team engagement
  • Leads advocacy activities of a more advanced and global strategic nature

Education / Work Experience:

  • BS in Engineering or other relevant field of study
  • Minimum of 10 years’ experience
  • Master's Degree or equivalent preferred
  • RAC desired

Knowledge / Competencies:

  • Demonstrated knowledge and application of regulatory requirements, including ISO, FDA, and International requirements
  • Demonstrated expertise in regulatory systems in a regulated environment
  • Demonstrated ability to manage complex projects
  • Demonstrated verbal, written, and interpersonal communication skills
  • Demonstrated ability to work in a team environment, interact effectively with management from other functions
  • Demonstrated ability to manage a multi-discipline, multi-technology, team-based organization and assume responsibility of quality, regulatory, and compliance targets
  • Demonstrated ability to initiate work
  • Demonstrated analytical ability
  • Demonstrated ability to make effective decisions
  • Experience with recruiting, people development
  • Influence across the organization

$171,500 - $379,000 salary plus bonus eligible + generally eligible for short-term and long-term financial incentives + benefits.  Individual pay is based on skills, experience, and other relevant factors.

Travel Percentage: 30%

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.

Top Skills

Fda
Iso
Regulatory Affairs

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