
Senior Regulatory Affairs Specialist
- Arden Hills, MN
- $82,600 per year
- Permanent
- Full-time
- Develop global strategies for regulatory approval of all medical device classifications
- Coordinate, author, compile, and submit U.S. and EU regulatory filings for new and modified products, including PMAs, PMA Supplements, pre-submissions, 510(k)s, Annual Reports, CE Mark submissions under MDR and US clinical investigation submissions
- Support requests from BSC International Regulatory personnel related to submissions, registrations, and change assessments and from clinical personnel related to international clinical investigation submissions
- Develop and maintain positive relationships with regulatory body reviewers
- Review Technical and Labeling documentation for inclusion in regulatory filings or as part of design changes
- Review product and manufacturing changes for compliance with applicable regulations and impact to regulatory filings
- Represent RA on cross functional projects which may include product development, sustaining changes, and continuous improvement efforts
- Support regulatory audits, as required
- In all actions, demonstrate a primary commitment to patient safety and product quality by maintaining compliance to the Quality Policy and all other documented quality processes and procedures
- A minimum of a Bachelor's Degree
- A minimum of 4 years of regulatory affairs or related experience
- Demonstrated experience authoring a variety of regulatory submissions for US and EU
- Computer skills, including experience with Microsoft Word, Excel, PowerPoint and Adobe Acrobat
- Previous experience in the medical device industry with Class II or III device submissions
- Experience working directly with FDA, notified bodies and/or international health authorities
- Strong technical, research and problem-solving skills
- Ability to articulate complex ideas clearly both verbally and in writing
- Team player with excellent interpersonal and communication skills
- Demonstrated ability to effectively manage multiple projects and priorities
- Works well in fast-paced cross-functional team environment