28 Medical Device Regulatory Submissions jobs

Irvine, California, US (On-site)

$177.5K / year

Description Job Title : Sr.

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…

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…

NL (On-site)

We believe that great healthcare is an essential safeguard of human dignity.

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.

Eden Prairie, Minnesota, US (On-site)

$131–143K / year

Why Join Bracco Medical Technologies?

Milano, Milan, IT (On-site)

Location Milan or Salerno Summary The Regulatory Affairs Portfolio Manager owns the regulatory strategy and technical file of Newel's medical device…

Portugal (Remote)

As Quality Assurance Officer, you will participate in the definition and implementation of Quality Management Systems (QMS) and preparation of…

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…

Germany (Remote)

kurzbeschreibung Wir unterstützen Hersteller dabei, sichere Medizinprodukte zu entwickeln, regulatorische Anforderungen effizient zu erfüllen und…

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.

Raleigh, North Carolina, US (On-site)

Description Position Summary: The Senior Manager, Regulatory Affairs provides strategic and operational leadership for global regulatory activities…

United States (Remote)

$170–185K / year

The Opportunity QuidelOrtho unites the strengths of Quidel Corporation and Ortho Clinical Diagnostics, creating a world-leading in vitro diagnostics…

Naples, Florida, US (On-site)

Requisition ID: 66438 Title: Senior Specialist, Regulatory Affairs - International (EMEA) Arthrex, Inc.

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.

Nehren, Baden-Württemberg, DE (On-site)

Überblick Bruker ermöglicht es Wissenschaftlern, bahnbrechende Entdeckungen zu machen und neue Anwendungen zu entwickeln, die die Qualität des…

Leuven, Flemish Brabant, BE (On-site)

At Terumo, we advance lifesaving medical technologies to benefit society.

Bay Area, California, US (Hybrid)

$195–250K / year

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

Germantown, Maryland, US (Hybrid)

$250–300K / year

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

Malden, Massachusetts, US (On-site)

Regulatory Affairs Manager AXIOMED SPINEFRONTIER Join our crew!