What are the responsibilities and job description for the Regulatory Affairs Specialist position at Heraeus?
Fridley
About Heraeus
Making displays foldable? Helping hearts beat with medical innovations? Or breathing new life into precious metals? As a family-owned global technology group we help our customers to always being one step ahead.
About Heraeus Medevio
Together we improve lives. At Heraeus Medevio, we bring lifesaving and life-changing medical devices to market through partnerships with medical device manufacturing companies. Backed by Heraeus Group, we are committed to the growth of our teams and organization by providing an open space for open minds.
To reach our vision of improving 100 million lives every year, we foster a culture of curiosity that thrives on challenge, continuous learning, growth, and the opportunity to try new things. With sites in the United States, European Union, and Asia, and over 2,200 employees worldwide, together, we will meet tomorrow's challenges today.
Position Summary
The Regulatory Affairs Specialists are responsible for initiating global regulatory strategies for new products and post-market changes. They review post-market changes for devices currently marketed to determine regulatory impact and prepare and/or review US FDA 510(k) regulatory submissions and 510(k) letters to file to obtain/maintain U.S. market clearance.
We are hiring two positions and these are based at the Fridley, MN location and Telecommuting permitted 4 days per week.
What You’ll Do Every Day
Curious? Apply now!
Heraeus is proud to be an employer that provides equal access to opportunities for all its employees. We provide fair and equal consideration to all qualified applicants, regardless of sex, gender identity, sexual orientation, race, color, religion, national origin, physical or mental disability, protected veteran status, age, or any other legally protected characteristic. A diverse and inclusive culture is at the heart of our Vision, Mission, and Values. We are dedicated to cultivating a workforce that reflects a broad spectrum of cultures, backgrounds, and perspectives.
We participate in E-Verify to confirm employment eligibility after hire. Learn more at www.e-verify.gov
Any further questions?
If you need any assistance or have questions, please contact hrdirect-americas@heraeus.com or visit our website at jobs.heraeus.com.
ReqID: 59356
About Heraeus
Making displays foldable? Helping hearts beat with medical innovations? Or breathing new life into precious metals? As a family-owned global technology group we help our customers to always being one step ahead.
About Heraeus Medevio
Together we improve lives. At Heraeus Medevio, we bring lifesaving and life-changing medical devices to market through partnerships with medical device manufacturing companies. Backed by Heraeus Group, we are committed to the growth of our teams and organization by providing an open space for open minds.
To reach our vision of improving 100 million lives every year, we foster a culture of curiosity that thrives on challenge, continuous learning, growth, and the opportunity to try new things. With sites in the United States, European Union, and Asia, and over 2,200 employees worldwide, together, we will meet tomorrow's challenges today.
Position Summary
The Regulatory Affairs Specialists are responsible for initiating global regulatory strategies for new products and post-market changes. They review post-market changes for devices currently marketed to determine regulatory impact and prepare and/or review US FDA 510(k) regulatory submissions and 510(k) letters to file to obtain/maintain U.S. market clearance.
We are hiring two positions and these are based at the Fridley, MN location and Telecommuting permitted 4 days per week.
What You’ll Do Every Day
- Initiate global regulatory strategies for new products and post-market changes.
- Review post-market changes for devices currently marketed to determine regulatory impact.
- Prepare and/or review US FDA 510(k) regulatory submissions and 510(k) letters to file to obtain/maintain U.S. market clearance.
- Prepare and/or review technical documentation for Health Canada and submit regulatory recertifications and change notifications as appropriate.
- Prepare and/or review appropriate documentation for initial submissions, change notifications, or renewals for EU MDR CE marked devices.
- Keep up to date with changing regulations and educate cross functional peers on new medical device regulations, such as EU MDR or relevant guidance published by the FDA, etc.
- Review international submissions to be submitted by our medical device company customers/partners.
- Review and approve changes to currently marketed devices to determine impact to regulatory clearances / approvals.
- Answer customer questions and provide letters/other documentation as is appropriate.
- Support Notified Body and other regulatory agency audits.
- Review and approve the rationale for reporting complaints to regulatory agencies and/or customers.
- Ensure understanding of all quality policy/system items that are applicable.
- Review and/or approve customer agreements for regulatory language that is relevant to the services provided.
- Ensure that the information provided through the FURLS registration system with the FDA and the MDALL database in Health Canada is up-to-date and accurate regarding establishments licensing, owner/operator and medical device listings.
- Update GUDID and/or EUDAMED database as needed for new and existing products.
- Bachelor's degree in Mechanical Engineering, Electrical Engineering, Biomedical Engineering, Pharmacy, Biology, or Chemistry and 5 years of experience as a Medical Device Regulatory Affairs Specialist, Medical Device Quality Engineer, or Medical Device Design Engineer
- Alternatively, Master's degree in Mechanical Engineering, Electrical Engineering, Biomedical Engineering, Pharmacy, Biology, or Chemistry 2 years of experience as a Medical Device Regulatory Affairs Specialist, Medical Device Quality Engineer, or Medical Device Design Engineer
- The five years of experience with a Bachelor’s degree or the two years of experience with a Master's degree must consist of experience with US and International medical device regulatory submissions, working with PMA or 510(k) devices, FDA, EU MDR, Health Canada, MHRA, MHLW, and TGA requirements, interactions with regulatory body/agency, and Vigilance/Adverse Event Medical Device Reporting.
Curious? Apply now!
Heraeus is proud to be an employer that provides equal access to opportunities for all its employees. We provide fair and equal consideration to all qualified applicants, regardless of sex, gender identity, sexual orientation, race, color, religion, national origin, physical or mental disability, protected veteran status, age, or any other legally protected characteristic. A diverse and inclusive culture is at the heart of our Vision, Mission, and Values. We are dedicated to cultivating a workforce that reflects a broad spectrum of cultures, backgrounds, and perspectives.
We participate in E-Verify to confirm employment eligibility after hire. Learn more at www.e-verify.gov
Any further questions?
If you need any assistance or have questions, please contact hrdirect-americas@heraeus.com or visit our website at jobs.heraeus.com.
ReqID: 59356
Salary : $110,178 - $120,000