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13 Medical Device Product Registration jobs

Showing 1–13 of 13 jobs

EC

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.

3 wk. ago

CM

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.

6 mo. ago

CB

Caledonia, Michigan, US (Hybrid)

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

2 wk. ago

B

Logan, Utah, US (On-site)

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

1 wk. ago

I

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…

2 yr. ago

MI

Regulatory Specialist

Medline Industries, LP

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…

2 wk. ago

S

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.

6 mo. ago

E

Cincinnati, Ohio, US (On-site)

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

10 yr. ago

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