Purpose:
The Senior Regulatory Affairs Specialist will provide regulatory support for New Product, Sustaining Engineering, and/or Operations project teams by identifying the appropriate domestic and international regulatory requirements and developing a regulatory strategy for global product commercialization. They will ensure product registrations are completed in accordance with project schedules. They will assess the domestic and/or international regulatory impact for process improvement and cost savings initiatives. In this position, they will prepare documentation to domestic and/or international regulatory authorities. They will communicate with regulatory agencies, as needed. They will work independently without direct supervision. They will perform other regulatory duties as assigned.
Duties and Responsibilities:
Required Qualifications:
Preferred Qualifications:
0-20% travel.
This position is not eligible for employer-based visa sponsorship.
Disclosure as required by applicable law, the annual salary range for this position is 60,000 to 95,000. The actual compensation may vary based on geographic location, work experience, education and skill level. The salary range is CONMED's good faith belief at the time of this posting.
Benefits:
CONMED offers a wide array of benefits to fit your unique needs. Visit our Benefits Page for more information.
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CONMED is an Equal Opportunity Employer & an Affirmative Action Employer. CONMED is a strong advocate of workforce diversity. All qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, sexual orientation, gender identity, national origin, disability, citizenship status, or veteran status.
If you feel you need a reasonable accommodation pursuant to the ADA, you are encouraged to contact us at 800-325-5900 option #3.