International Senior Regulatory Affair Specialist jobs

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Sr. Specialist / Specialist, International Regulatory Affair...
Saint Joseph, MO 64506
Acquire required documentation for any type of submission; communicates and give guidance to other departments regarding format and timeline expectations...
Sr Principal Regulatory Affairs Specialist
Menlo Park, CA 94025
The Sr. Principal Regulatory Specialist will represent Regulatory Affairs on core project teams and be responsible for drafting regulatory submissions and...
Desired:Microsoft WordClinical TrialsAdobe AcrobatMicrosoft OfficeExceland 1 more...
Senior Regulatory Affairs Specialist (2018)
NeuroLogica
Danvers, MA 01923
Understand and provide input for compliance to various global regulatory requirements, such as 21 CFR 803, 806, and 820, ISO 13485, CMDCAS, Medical Device...
Desired:Microsoft WordMicrosoft OfficeISO 13485ExcelMicrosoft Powerpoint
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Sr. Regulatory Affairs Specialist
$105,000 a year
In this role will develop strategies and submissions for complex projects and issues related to global submissions, regulatory documents, investigations...
Desired:Time ManagementExcelMicrosoft WordMicrosoft Powerpoint

Senior International Regulatory Affairs Specialist

Tampa, FL 33602 (Downtown area)
As Subject Matter Expert, advises Global / US / International Regulatory, submission teams on all International Product Registration requirements, and...
Desired:Management ExperienceProject ManagementMedical TerminologyMicrosoft OfficeMilitary Experience

Sr. Regulatory Affairs International Specialist

Warwick, RI
This position is responsible for writing, supporting, and assisting in gaining approval of product registrations and other submissions to International...

Senior International Regulatory Affairs Specialist

Seattle, WA 98109 (Westlake area)
Responsible for the implementation of regulatory strategies through coordination and preparation of submission documents for the registration of new products...
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Regulatory Specialist/Sr. Specialist

Warwick, RI
Key responsibilities involve assurance that clinical evaluations and new product submissions are in compliance with applicable global medical device...

Regulatory Senior Specialist - Multiple Locations

Regulatory & Quality Solutions LLC
United States
Support pre-and post-market activities including, but not limited to, Investigational Device Exemptions, pre-market notification applications [510(k...
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Sr. Regulatory Affairs International Specialist

Warwick, RI
This position is responsible for writing, supporting, and assisting in gaining approval of product registrations and other submissions to International...

Sr Regulatory Affairs Specialist - International

Santa Rosa, CA 95403
The Cardiac and Vascular Group brings all of our cardiac and vascular businesses together into one cross-functional, collaborative operating unit to employ...
Desired:Time ManagementClinical TrialsISO 13485Negotiation

Sr. Regulatory Affairs Specialist

Clinovo
San Francisco Bay Area, CA
The Senior Regulatory Affairs Specialist will represent RA on project core teams, perform the coordination and preparation of document packages for...
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Regulatory Specialist/Sr. Specialist

Warwick, RI
Key responsibilities involve assurance that clinical evaluations and new product submissions are in compliance with applicable global medical device...

Senior Regulatory Affairs Specialist

Sunnyvale, CA
Responsibilities include reviewing design input/output, performing regulatory assessments to determine the impact of design/process changes, maintaining...
Desired:Project Management
Senior Regulatory Affairs Specialist
Fort Wayne, IN
This is a critical role that will provide oversight to regulatory activities necessary to obtain and maintain regulatory approvals within the United States...
Desired:Quality ManagementISO 13485
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Senior RA Specialist
Confidential
Golden, CO
Reviews domestic and international labeling for compliance to labeling requirements, including content, format, 510(k) and regulatory registration impact...
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