Skip to Job Postings

Medical Device Regulatory Affairs Jobs
69,053 Jobs within 5000 miles of Ashburn, VA

  • Full-Time

Must have 3-5 years of experiences in Medical Device Regulatory Affairs (within the clinical industry) Have working knowledge in EU MDR Have working knowledge in Regulatory Change Assessment in Have ...

  • Full-Time

A well known multinational medical device company is looking for regulatory affairs associates to join their team long term and support their Class II and III devices: WHAT YOU'LL DO Prepares robust ...

Beckman Coulter, Inc.

Staff Regulatory Affairs, Medical Device- Remote

Beckman Coulter, Inc. New York, NY

Remote

  • Full-Time

The Staff Regulatory Affairs, New Product Development for Beckman Diagnostics is a high-level ... Experience with medical device development process, design changes and design controls ...

Artio Medical, Inc.

Regulatory Affairs Specialist

Artio Medical, Inc. Menlo Park, CA
  • Full-Time

Regulatory Affairs masters and/or 2 years in medical device industry * Experience with 510(k), PMA, IDE applications, and US device regulations and/or experience with EU and other international ...

Systems Planning and Analysis, Inc.

Senior Scientist - Regulatory Affairs

Systems Planning and Analysis, Inc. Lorton, VA
  • Full-Time

... drug and device development for products regulated by the FDA. * Expertise in non-clinical ... medical devices. Employment Type: FULL_TIME

Zoll Medical Corporation

Director, Regulatory Affairs

Zoll Medical Corporation San Jose, CA
  • Full-Time

The Director of Regulatory Affairs is responsible for developing, implementing, and leading both ... Regulatory support of new and marketed Medical device products. * Liaison with FDA and other ...

1801 Bard Access Systems, Inc

Senior Manager, Regulatory Affairs

1801 Bard Access Systems, Inc Salt Lake City, UT
  • Full-Time

At least 10years Regulatory Affairs experience in global medical device regulations strongly preferred * Experience working with software, capital equipment, cybersecurity, interoperability, and ...

ZMC-US MA ZOLL Medical Corporation

Principal Regulatory Affairs Specialist

ZMC-US MA ZOLL Medical Corporation Anchorage, AK
  • Full-Time

... medical device regulatory experience * Experience with the interpretation and application of ... Regulatory Affairs Certification (RAC) by the Regulatory Affairs Certification Board (RACB) desired

Katalyst Healthcares & Life Sciences

Regulatory Affairs Specialist

Katalyst Healthcares & Life Sciences Fort Worth, TX
  • Full-Time

... international medical device regulations * The individual leads the submission of licenses and ... Manages the personnel activities of the Regulatory Affairs and Document Control departments ...

Principal International Regulatory Affairs Specialist (RA QA / Compliance / Health Care / Medical Device) Responsibilities The Principal International RA Specialist will plan and execute global ...

Remote

  • Full-Time

Demonstrated ability to lead medical device regulatory submissions * Proven success in preparing ... Regulatory Affairs Certified RAC (RAPS) * Experience with vascular access medical devices Skills

Shockwave Medical

Sr. Regulatory Affairs Specialist

Shockwave Medical Santa Clara, CA
  • Full-Time

Shockwave Medical aims to establish a new standard of care for medical device treatment of ... The Sr. Regulatory Affairs Specialist combines knowledge of scientific, regulatory and business ...

True Digital Surgery

Manager of Regulatory Affairs

True Digital Surgery Goleta, CA
  • Full-Time

Our medical imaging and guidance system employs advanced real-time 3D graphic capabilities and ... Establish device classification, predicate strategy, clinical protocols, clinical evaluations ...

USA - Smith & Nephew, Inc.

Regulatory Affairs Specialist II (Hybrid)

USA - Smith & Nephew, Inc. Austin, TX
  • Full-Time

Bachelor's degree or equivalent work experience, preferably in a scientific or technical discipline Experience: * 2+ years' experience in Regulatory Affairs (medical device industry preferred ...