Regulatory Affairs Specialist Jobs in Bridgewater (NJ)
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Search Results - Regulatory Affairs Specialist Jobs in Bridgewater (NJ)
The Fountain Group LLC-Bridgewater (NJ)
The Fountain Group are a national staffing firm and are currently seeking a Regulatory Affairs Lead for a prominent Pharmaceutical client of ours. This position is in Bridgewater, NJ (Hybrid Role). Details for the position are as follows:
Job...
resume-library.com -
Spectraforce Technologies Inc-Bridgewater (NJ)
for the authoring by reaching out to appropriate internal/external functions such as quality, manufacturing, Global Regulatory Affairs (GRA), technical experts from global locations or contract manufacturing organizations (CMOs), or alliance partners.
He/She...
mindmatch.ai -
Mindlance-Bridgewater (NJ)
US Regulatory Affairs Lead – Personal Care Category
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SCOPE OF RESPONSIBILITIES:
• He/She will be accountable to support regulatory for Personal Care...
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B. Braun Medical Inc. (US)-Bethlehem (PA), 39 mi from Bridgewater (NJ)
the department.
• May oversee and direct the work of other Regulatory Affairs professionals.
The job function listed is not exhaustive and shall also include any responsibilities as assigned by the Supervisor from time to time.
Expertise: Knowledge & Skills...
mindmatch.ai -
Integrated Resources, Inc-Bridgewater (NJ)
and are organized in a manner to facilitate agency review
Education:
" Minimum B.S.; M.S., Pharm D, MD, PhD or equivalent preferred
" Regulatory Certification (RAC) preferred
" Minimum 5 years in Regulatory Affairs, including leadership roles
" Established...
resume-library.com -
Center Valley (PA), 40 mi from Bridgewater (NJ)
products and communicate within the department.
• May oversee and direct the work of other Regulatory Affairs professionals.
The job function listed is not exhaustive and shall also include any responsibilities as assigned by the Supervisor from time...
icims.com -
Katalyst Healthcares & Life Sciences-Edison (NJ), 14 mi from Bridgewater (NJ)
Responsibilities:
This position is responsible for the preparation of regulatory submissions required to market medical devices in both the U.S. and Europe, support of international product registrations and related regulatory affairs activities...
resume-library.com -
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