Senior Regulatory Affairs Specialist

The Senior Regulatory Affairs Specialist plays a critical role in ensuring regulatory compliance and supporting cross-functional teams in the preparation, submission and tracking of regulatory documentation. This role involves proactive communication of regulatory changes, fostering trust within the organization.

This is an onsite role based in Denver, CO.

• Assist in executing product registrations for USFDA submission (510(k), CE-mark certificate and other international registrations, which includes creating and maintaining Technical Files and supportive documents.
• Prepare global regulatory files/submissions for product registration as assigned.
• Assist in the review of proposed design changes and ECOs to assess regulatory impact.
• Assemble information required for domestic and international submissions.
• Assist the Specialists in assembly and update of Technical Files and Dossiers.
• Provide timely review of product labeling for regulatory compliance.
• Compile information for Medical Device Listings and Certificates to Foreign Government.
• Research and compile information required for customs and sales force requests.
• Assist as needed with marketing collateral reviews.
• Perform other related duties and special projects as required by management.

• Bachelor's Degree in science, engineering or related field
• 2+ years experience in a Regulatory Affairs role
• Authoring and/or leading regulatory submissions (i.e.: 510(k), EU technical documentation)

• M.S. in a technical field or MBA preferred
• Additional Regulatory certifications preferred
• Experience with in the Medical Device industry preferred

• Ability to execute assignments independently as assigned
• Must possess strong organization skills
• Must possess strong written and verbal communication skills.
• Demonstrated ability to handle multiple priorities simultaneously.

This position is not eligible for employer based sponsorship. Disclosure as required by applicable law, the annual salary range for this position is $70,000 - $100,000. 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.

This job posting is anticipated to close on March 15, 2026. We may, however, extend this time period, in which case the posting will remain available on  Please submit your application as soon as possible as we will be reviewing applications on a rolling basis as we receive them.

• Competitive compensation
• Excellent healthcare including medical, dental, vision and prescription coverage
• Short & long term disability plus life insurance -- cost paid fully by CONMED
• Retirement Savings Plan (401K) -- CONMED matches your contributions dollar for dollar, with the potential for up to 7% per pay period
• Employee Stock Purchase Plan -- allows stock purchases at discounted price
• Tuition assistance for undergraduate and graduate level courses

Know someone at CONMED? Have them submit you as a referral before applying for this position to be eligible for our Employee Referral Program incentives!

CONMED is an equal opportunity employer and does not discriminate on the basis of any legally protected status or characteristic. Protected veterans and individuals with disabilities are encouraged to apply. Know Your Rights:
Workplace Discrimination is Illegal Poster reaffirms this commitment.

Colorado Residents:
In any materials you submit, you may redact or remove age-identifying information such as age, date of birth, or dates of school attendance or graduation. You will not be penalized for redacting or removing this information.

If you feel you need a reasonable accommodation pursuant to the ADA, you are encouraged to contact us at  option #5.