Job Details
We are currently seeking a Senior Regulatory Affairs Specialist
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What you will do
- Support R&D, Marketing and Manufacturing teams with regulatory assessments of proposed changes or product transfers.
- Identify requirements and potential obstacles for market access distribution (federal, provincial/territorial state, reimbursement, purchasing groups, etc.).
- Assist in the development of regulatory strategy and updates strategy based upon regulatory changes.
- Evaluate proposed products for regulatory classification and jurisdiction.
- Determine requirements (local, national, international) and options for regulatory submission, approval pathways, and compliance activities.
- Prepare and submit electronic and paper regulatory submissions according to applicable regulatory requirements and guidelines for required products.
- Provide regulatory information and guidance for product development and planning throughout the product lifecycle to the regulatory groups and others within the organization.
- Communicate and interact with regulatory authorities throughout the development and review process of a regulatory submission through appropriate communication tools.
- Evaluate proposed pre-clinical, clinical, and manufacturing changes for regulatory filing solutions and propose plans/strategies (if appropriate) for changes that do not require submissions.
- Identify, monitor, and submit applicable reports or notifications to regulatory authorities during the clinical research process.
- Maintain current product registrations and assist with processing registration changes when required.
What you need
- Bachelor’s degree in an Engineering, Science, or equivalent field.
- Minimum of 3 years of experience in an FDA or highly regulated industry required.
- Minimum of 2 years in a Regulatory Affairs role required.
Preferred
- RAC certification or Advanced Degree (Masters in Regulatory Affairs).
- Previous experience with US Class II/III medical devices.
- Experience authoring regulatory submissions for product approval.
- Experience interacting with regulatory agencies.
- $88,800.00 - 142,300.00 USD, Annual salary plus bonus eligible + benefits. Individual pay is based on skills, experience, and other relevant factors.
Required Skills
Company Details
Stryker
Kalamazoo, MI, United States
Stryker is a global leader in medical technologies and, together with our customers, we are driven to make healthcare better. We offer innovative... Read more