Work Flexibility: Hybrid

Stryker is hiring a Senior Regulatory Affairs Specialist to join our Sage business in Cary, Illinois! In this role, you will support product compliance and market access by applying your understanding of regulatory frameworks, requirements, and procedures throughout the product lifecycle.

What you will do:

Assesses regulatory intelligence to support the development and refinement of local, regional, and global regulatory strategies.

Evaluates the regulatory environment to provide guidance throughout the product lifecycle (concept to post-market) ensuring compliance and facilitating market access.

Anticipates and addresses regulatory obstacles and emerging issues by developing proactive solutions.

Determines regulatory classification, jurisdiction, and submission requirements (local, national, international), including approval pathways and compliance activities.

Provides regulatory input and technical guidance on quality, preclinical, clinical, and manufacturing data to meet applicable standards.

Assesses the acceptability of documents for submission and evaluates proposed changes to determine regulatory impact and filing strategies.

Prepares and submits regulatory dossiers (electronic/paper), and monitors agency reviews through effective communication with authorities.

Advises cross-functional teams on regulatory requirements for claims, labeling, and market access (e.g., federal, state/provincial, reimbursement, purchasing groups).

Leads or supports interactions with regulatory bodies, including pre-approval inspections, GCP inspections, panel meetings, and advisory committees.

Develops and implements regulatory SOPs and procedures; supports organizational compliance through training and cross-departmental collaboration.

Tracks and submits required reports/notifications during clinical research and ensures data supports regulatory strategy and product claims.

What you need:

Required:

Bachelor’s degree required. Preferred to be in Engineering, Science, Legal or related.

2+ years of regulatory experience.

Preferred:

New product development (NPD) experience is a plus.

RAC(s) preferred.

Manages and executes regulatory projects, including writing, coordination, and technical/scientific activities.

Demonstrates strong interpersonal skills by engaging diverse perspectives and fostering collaboration across teams.

Navigates organizational dynamics effectively, balancing competing priorities and aligning actions with strategic goals.

Travel Percentage: None

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.