18 Regulatory Submissions Specialist jobs

United States (Remote)

This is a remote position.

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?

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…

Naples, Florida, US (On-site)

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

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.

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…

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

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

San Francisco, California, US (On-site)

$145–168K / year

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

NL (On-site)

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

Malden, Massachusetts, US (On-site)

Regulatory Affairs Manager AXIOMED SPINEFRONTIER Join our crew!

Cincinnati, Ohio, US (On-site)

Regulatory Affairs Specialist position: • Exhibit a competence in US & foreign government regulations regarding the manufacture & distribution of…

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…

Leuven, Flemish Brabant, BE (On-site)

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

Paris, Île-de-France, FR (On-site)

Job Summary We are seeking an experienced Medical Device Vigilance Specialist with deep expertise in French vigilance requirements and direct…

Budapest, HU (Hybrid)

Overview As a Clinical Research Associate , you will support the clinical performance and post-market surveillance of in vitro diagnostic products.

Portugal (Remote)

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