Medical Device Regulatory Associate Jobs

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Quality Assurance Specialist  

Deephealth - Somerville, Massachusetts

. Participation in regulatory audits Excellent written and oral communication skills To Ensure Success In This Role, You Must Have: Bachelor’s degree in relevant field (or equivalent experience, i.e. Associates

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from: resume-library.com - 14 days ago

Senior Counsel, Regulatory  

Baxter International Inc - Deerfield, Illinois, USA

. The position involves handling major projects, transactions or matters under the supervision of Associate General Counsel, Regulatory and has principal responsibility for planning and directing more discrete $216,000 to $324,000

from: Ivyexec.com - 13 days ago

Regulatory Affairs Specialist I (Depuy Synthes/Spine) - Medical Device Business Services, Inc. (2 of 2)  

Johnson & Johnson - Raynham, MA

, or similar. Minimum 0-2+ years' of regulatory experience in a highly regulated industry, preferably in medical device or pharmaceutical. Relevant internship experience may be considered . Demonstrated

from: Dice.com - 10 days ago

Clinical Studies Spt Coord IV  

Medtronic - North Haven, CT

's or Bachelor's degree preferred 7+ years' experience in clinical study administration or related experience Clinical research/study coordination experience at Medtronic or medical device industry Experience

from: Dice.com - 16 days ago

Senior Quality Compliance Engineer  

ConvaTec - Deeside, United Kingdom

quality management, Site Quality Leads, R&D, Regulatory Affairs, Clinical Affairs, Quality Engineering, Quality Associates and all other functions as required by the role Travel Requirements: Periodic

from: Ivyexec.com - 17 days ago

Director of Healthcare Technology Management  

Virtus Healthcare Staffing, LLC - Las Vegas, Nevada

planning. Strong understanding of regulatory requirements for medical devices (CMS, TJC, CLIA, AABB, NRC, State, Local). Excellent communication, presentation, and interpersonal skills. Proficient

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from: resume-library.com - 23 days ago

Engineer III, Validation  

Thermo Fisher Scientific - Middletown, Virginia, United States of America

with progressively increasing responsibilities is required. Associate degree and 8+ years of relevant experience in the pharmaceutical, medical device, or in-vitro diagnostics industry. Preferred Qualifications

from: jobs.thermofisher.com - More than 30 days ago

Staff Validation Engineer  

Thermo Fisher Scientific - Middletown, Virginia, United States of America

industry with progressively increasing responsibilities is required. Associate degree and 15+ years of relevant experience in the pharmaceutical, medical device, or in-vitro diagnostics industry

from: jobs.thermofisher.com - More than 30 days ago

Sr. Project Engineer, SDS  

FUJIFILM Holdings America Corporation - Atlanta, GA

and procedures. Comply with all applicable U.S. Food and Drug Administration (U.S. FDA) medical device regulatory requirements, applicable ISO 13485 standard requirements and all other applicable laws, regulations

from: careerbuilder.com - 19 days ago


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