Regulatory Affairs Manager
Listed on 2026-02-06
-
Management
Healthcare Management -
Healthcare
Healthcare Management
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Corner Stone Professional Placement provided pay rangeThis range is provided by Corner Stone Professional Placement. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.
Base pay range$/yr - $/yr
Direct message the job poster from Corner Stone Professional Placement
Corner Stone Professional Placement is seeking a Regulatory Affairs Manager for a medical device manufacturing client in the Frisco, TX area. As the Regulatory Affairs Manager, you will be responsible for overseeing regulatory processes and ensuring submissions comply with U.S. and European medical device standards. You will thrive in this role if you have leadership experience, strong regulatory knowledge including 510(k) and CE marking submissions, and a background in biomedical or science disciplines.
This is an exciting opportunity to lead in a high-impact, direct hire role with a company committed to overhauling and improving its Regulatory Affairs operations.
What You’ll Actually Do as the Regulatory Affairs Manager:
- Prepare and manage regulatory submissions in compliance with U.S. and EU medical device regulations
- Maintain and update technical files for CE marking and 510(k) approvals
- Lead and guide a team of regulatory professionals
- Monitor evolving compliance standards and ensure internal policies meet industry requirements
- Collaborate with cross-functional teams to support new product development and international market access
What You’ll Need to Succeed as the Regulatory Affairs Manager:
- Bachelor’s degree in biomedical engineering or a related science field
- At least 3 years of experience in medical device regulatory affairs
- Proven leadership or team management experience
- Experience with CE marking, 510(k) submissions, and technical file maintenance
- Strong organizational, analytical, and communication skills
It’s a bonus if you’ve used:
- EU MDD standards in a medical device regulatory setting
- Documented success in process improvement within a regulatory team
Why This Role Fits Your Life:
Employment type:
Direct Hire
Schedule:
Monday–Friday, 7:00 AM–4:00 PM or 8:00 AM–5:00 PM
Salary/Pay: $90,000–$130,000/year (commensurate with experience)
Location: 100% On-site
Benefits:
Medical, Dental, Vision, Life, AD&D, Disability, HSA, FSA, 401(k) with matching, Employee Assistance Program, Tuition Reimbursement, Paid Holidays, Paid Vacation, and more!
- Seniority level
Mid-Senior level
- Employment type
Full-time
- Job function
Quality Assurance, Management, and Legal - Industries Medical Equipment Manufacturing and Manufacturing
Referrals increase your chances of interviewing at Corner Stone Professional Placement by 2x
Inferred from the description for this jobMedical insurance
Vision insurance
401(k)
Disability insurance
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