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Regulatory Affairs Manager

Job in Frisco, Collin County, Texas, 75034, USA
Listing for: CornerStone Professional Placement
Full Time position
Listed on 2026-02-06
Job specializations:
  • Management
    Healthcare Management
  • Healthcare
    Healthcare Management
Salary/Wage Range or Industry Benchmark: 90000 - 130000 USD Yearly USD 90000.00 130000.00 YEAR
Job Description & How to Apply Below

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Corner Stone Professional Placement provided pay range

This 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
  • Seniority level

    Mid-Senior level
Employment type
  • Employment type

    Full-time
Job function
  • 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 job

Medical insurance

Vision insurance

401(k)

Disability insurance

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