53 FDA jobs

United States (Remote)

This is a remote position.

Logan, Utah, US (On-site)

Overview This role is responsible for ensuring that all products comply with applicable global regulatory requirements throughout their…

Malden, Massachusetts, US (On-site)

Regulatory Affairs Manager AXIOMED SPINEFRONTIER Join our crew!

Caledonia, Michigan, US (Hybrid)

Regulatory Affairs Specialist Job Description Who We Are: Marketlab is a market leading healthcare solutions organization specializing in the design,…

Greer, South Carolina, US (On-site)

$150–170K / year

Alltrista Plastics LLC, is a subsidiary of Jadex Inc., and is a leading manufacturer in high-volume, precision injection molded parts.

Bristol, England, GB (On-site)

Position Overview Are you passionate about shaping the future of medical device quality?

Milano, Milan, IT (Hybrid)

€37–45K / year

As a Quality Assurance Specialist at Empatica, you will be a key member of the Quality and Regulatory Department, supporting the maintenance of the…

Alameda, California, US (On-site)

$90–125K / year

In this role, you will work with the team that ensures that Penumbra products are approved for use in countries around the world, thereby helping to…

Sarasota, Florida, US (On-site)

General Summary The Regulatory Affairs Manager will be responsible for leading ASO’s Regulatory and Compliance directives carrying out a wide range…

Germantown, Maryland, US (Hybrid)

$250–300K / year

Overview At QIAGEN, we are driven by a simple but powerful vision: making improvements in life possible.

Caledonia, Michigan, US (Hybrid)

Regulatory Affairs Specialist Job Description Who We Are: Marketlab is a market leading healthcare solutions organization specializing in the design,…

San Mateo, California, US (Hybrid)

Lead the Future of Dentistry.

San Francisco, California, US (On-site)

$188–240K / year

Heartflow is a medical technology company advancing the diagnosis and management of coronary artery disease, the #1 cause of death worldwide, using…

San Francisco, California, US (Hybrid)

$215–270K / year

Heartflow is a medical technology company advancing the diagnosis and management of coronary artery disease, the #1 cause of death worldwide, using…

Voisins-le-Bretonneux, Paris, FR (On-site)

CMSChargé(e) Assurance Qualité- Dispositif Médical Description de l'emploi ZOLL est une société du groupe Asahi Kasei, qui développe, fabrique et…

Irvine, California, US (On-site)

$177.5K / year

Description Job Title : Sr.

Winston-Salem, North Carolina, US (On-site)

What we are looking for: Plans, organizes and implements strategies and activities required to procure regulatory approval for new and revised product lines.

Winston-Salem, North Carolina, US (On-site)

What we are looking for: Plans, organizes and implements strategies and activities required to procure regulatory approval for new and revised product lines.

Alameda, California, US (Hybrid)

$77–98K / year

In this role, you will work with the team that ensures that Penumbra products are approved for use in countries around the world, thereby helping to…

Issy-les-Moulineaux, Paris, FR (On-site)

About Withings: Withings designs connected health devices (scales, blood pressure monitors, ECG watches, an under-mattress sleep sensor) and AI-based…