13 Product Registration jobs

Logan, Utah, US (On-site)

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

Caledonia, Michigan, US (Hybrid)

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

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.

Leuven, Flemish Brabant, BE (On-site)

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

Leuven, Flemish Brabant, BE (On-site)

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

Bratislava, SK (On-site)

About the Company: Our client is a global leader in producing high-tech medical and aesthetic devices, known for their use of valuable materials and…

Cincinnati, Ohio, US (On-site)

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

Pratica di Mare, Pomezia, Lazio, IT (On-site)

€39.8–64.1K / year

At Johnson & Johnson, we believe health is everything.

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.

Châteaubriant, Pays de la Loire, FR (Hybrid)

Afin de placer nos dispositifs médicaux sur le marché européen, le département Qualité/Affaires Réglementaires veille à ce que tous les produits…

Hechingen, Baden-Württemberg, DE (Hybrid)

Es ist ein gutes Gefühl zu wissen, wofür Du täglich Dein Bestes gibst.

Belgrade, RS (On-site)

QMS Specialist (Medical devices) Our client is a company that specializes in designing and developing mission-critical healthcare information system solutions.

Germany (Remote)

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