Medical Device Regulatory Affairs Jobs

Integrated Resources, Inc ( IRI ) - ST Louis, MO, United States

Your Role: With minimal supervision, the Regulatory Affairs Expert-Medical Devices manages assigned regulatory tasks related to health authority notifications, submissions, and registrations

from: linkedin.com - 4 days ago

Shepherd Regulatory Search - Marlborough, MA, United States

approvals to market devices throughout the product development lifecycle while building and managing a regulatory team. Responsibilities: Develop strategies for regulatory approval of medical devices

from: linkedin.com - 12 days ago

Randstad - st louis, missouri

, we have the ideal position for you! The Regulatory Affairs Expert-Medical Devices manages assigned regulatory tasks related to health authority notifications, submissions, and registrations regarding renewals and new $30 - $33.10 per hour

from: randstadusa.com - 7 days ago

Bright Uro - Irvine, CA, United States

Uro markets, including Registration, Non-Conformities, Product Recalls, Field Actions and Medical Device Reporting. Maintain and update regulatory files and binders. Education and Work Experience

from: linkedin.com - 14 days ago

Lumicity - Akron, OH, United States

The ideal Senior Regulatory Affairs Specialist candidate will come with a strong regulatory affairs background working within the Medical Device industry. This candidate will also possess proficient

from: linkedin.com - 5 days ago

Randstad Life Sciences US - , MO, United States

Regulatory Affairs Expert-Medical Devices 1 Year (Extendable & potential to convert) St Louis, MO Max PR: $25-33/hr Your Role: With minimal supervision, the Regulatory Affairs Expert-Medical Devices

from: linkedin.com - 4 days ago

Randstad Life Sciences US - , MO, United States

Regulatory Affairs Expert-Medical Devices 1 Year (Temp to perm) St Louis, MO (Hybrid 2-3 days onsite) Pay: $33.00/hr Your Role: With minimal supervision, the Regulatory Affairs Expert-Medical Devices

from: linkedin.com - 4 days ago

Barrington James - , CA, United States

Senior Regulatory Affairs Specialist (Medical Devices) - Hybrid (Bay Area) Our client is a growing Imaging Medical Device company that is making a meaningful impact on patient lives. They are looking

from: linkedin.com - 7 days ago

Redbock - an NES Fircroft company - Irvine, CA, United States

+ years in medical device regulatory affairs Understanding of current FDA and International regulations, guidance and standards applicable to medical device products Excellent written and verbal

from: linkedin.com - 12 days ago

GForce Life Sciences - Newark, NJ, United States (+1 location)

Requirements B.S. Degree, preferably in Engineering 2+ years of prior complaint-handling experience with a medical device company Quality experience Nice to Have Prior experience processing medical device

from: linkedin.com - 3 days ago