What are the responsibilities and job description for the Principal Regulatory Affairs Specialist position at Linvatec Corporation?
The Advanced Surgical Principal Regulatory Affairs Specialist provides regulatory input for new product and sustaining engineering project teams, developing a regulatory strategy for global commercialization of products. The specialist should be capable of identifying both domestic and international regulatory requirements early in product life cycles and coordinating the product registrations to meet company milestones and initiatives. Key Duties and Responsibilities: Represent the Regulatory organization on cross functional teams to develop and implement regulatory strategies and carry out associated team output responsibilities. Prepare global regulatory files/submissions for product registration as assigned. Review and approve proposed design changes and ECOs to assess regulatory impact. Work collaboratively with other RA staff to ensure consistency of RA inputs and strategies. Provide regulatory support for on-going global product registrations as assigned. Provide timely review and approval of product labeling for regulatory compliance. Participate in all activities associated with product recalls (regulatory agency communications, customer communications, status reports). Establish and maintain product recall files. May interface with other ConMed business units/affiliates/distributors as assigned. Perform other related duties and special projects as required by management. This will be a hybrid role - 50% onsite in Denver, 50% remote Minimum Requirements: Bachelor’s Degree in science, engineering or related field 5 years experience years in a regulatory, quality, or similar position. Preferred Requirements: M.S. in a technical field or MBA preferred Additional Regulatory certifications preferred Experience within the Medical Device industry preferred Other Attributes: 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. US/EU submission experience, including authoring and receiving approvals and interaction with regulated bodies (FDA, Notified Body, etc.). Physical Requirements: Must be able to sit/stand for 8 hours Disclosure as required by applicable law, the annual salary range for this position is $80,000 - $130,000. 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. 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. Benefits: CONMED offers a wide array of benefits to fit your unique needs. Visit our Benefits Page for more information. 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 & 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. The Know Your Rights: Workplace Discrimination is Illegal Poster and Pay Transparency Nondiscrimination Provision reaffirm 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 800-929-7176 option #5. CONMED Corporation is a progressive, global medical device company. Through thoughtful leadership, innovation and team work, we are changing the future of medicine. Our 3,500 employees worldwide make meaningful contributions, positively impact the business, and advance in their careers as our company and product portfolio grows. We are a leader in Orthopedics, General Surgery, Gynecology, Gastroenterology, Pulmonology, and Anesthesiology and our employees enjoy challenging and diverse job opportunities across these varied specializations. We are headquartered in upstate New York with additional domestic facilities in FL, CA, MA, CO, and GA. We have an international presence in more than 20 locations throughout Europe, Australia, Latin America, Asia, North America, and the Middle East.
Salary : $80,000 - $130,000
