Regulatory Affairs Manager-Medical Devices

New England or Western Pennsylvania and work remotely with the ability to be onsite in Bowdoin, Maine or Greenville, PA as needed. FHC, Inc. has served the neuroscience community for over 50 years. With a guiding principle of innovation through collaboration, FHC designs, manufactures, and internationally markets products that provide customizable, pioneering solutions for neuroscientists, neurologists, and neurosurgeons and has been recognized on the Best Places to Work in Maine list for 2026.

The Regulatory Affairs Manager is responsible for leading and overseeing the Company's global regulatory affairs activities to ensure compliance with applicable medical device regulations and standards in all markets where products are manufactured, marketed, distributed, or sold. This position develops and executes regulatory strategies that support product development, market access, business growth, and post-market compliance activities.

About Skillcloud HCM

FHC, Inc

Responsibilities

• Bowdoin, Maine OR Greenville, PA (Remote)
• FHC, Inc

to be based in

• Develop and implement global regulatory strategies that support product development, commercialization, and lifecycle management of medical devices.
• Provide regulatory leadership and guidance throughout all phases of product design, development, verification, validation, release, and post-market support.

Advise

• executive leadership on regulatory risks, opportunities, emerging regulations, and business impacts.
• Lead, mentor, and develop Regulatory Affairs personnel.
• Oversee preparation, review, submission, and maintenance of regulatory filings
• Ensure timely maintenance of product registrations in all approved markets.
• Manage interactions with regulatory authorities, notified bodies, distributors, and international representatives.

Requirements

• Bachelor's degree in Engineering, Biomedical Engineering, Life Sciences, Regulatory Affairs, Quality, or related technical discipline required
• Minimum of 7-10 years of medical device regulatory affairs experience.
• Minimum of 3 years of leadership, supervisory, or project leadership experience
• Demonstrated experience with FDA submissions, international registrations, and global market access activities.
• Experience with FDA, MDR, UK, Canada, and MDSAP requirements
• Experience supporting ISO 13485-certified and FDA-regulated environments required

Preferred

• Master's degree preferred.
• Experience with Class II and/or Class III medical devices preferred.
• RAC (Regulatory Affairs Certification), ASQ Certified Quality Auditor (CQA), ASQ Certified Quality Engineer (CQE), ISO 13485 Lead Auditor Certification preferred.

Pay

• Salary in the range of $
• 120-140K

Benefits

• Health and
• options
• 401K with company match
• Employee Stock Ownership Plan
• Generous PTO, holiday pay, paid sick time
• Up to $1000/ year for approved professional development
• Options for Life Insurance, HSA and DCA Accounts
• Flexible work schedule with the opportunity for hybrid work 1-2 days/week

Skillcloud HCM Solutions has been engaged to manage this search. NO PHONE CALLS OR RECRUITERS PLEASE

I certify that the information contained in this application and resume is accurate and complete to the best of my knowledge. I understand that providing false, misleading, or incomplete information may result in the denial of employment or termination of employment if hired.

Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, ancestry, familial status, age, physical or mental disability, pregnancy, sexual orientation, gender identity, genetic information, veteran status, or any other characteristic protected by law.