Regulatory Affairs Specialist Jobs
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Search Results - Regulatory Affairs Specialist Jobs
GForce Life Sciences-Alameda (CA)
Regulatory Affairs Specialist
Onsite in Alameda, CA
Summary:
Our client is seeking a Regulatory Affairs Specialist for a 12-month W2 contract with the possibility of extension. This role offers a starting salary of $85K/year and involves...
mindmatch.ai -
On-Board Companies-Stamford
On-Board Scientific is hiring a Regulatory Affairs Specialist in Stamford, CT - Hybrid Role
For immediate consideration please send your resume to
Subject Line: Position Title and State you are located
About Us:
On-Board Services, Incorporated...
resume-library.com -
Lumicity-Los Angeles
Job Title: Regulatory Affairs Specialist
Our client is seeking an experienced Regulatory Affairs Specialist to lead regulatory strategy and submissions for medical devices. This role involves ensuring compliance with global regulatory requirements...
mindmatch.ai -
Abbott Laboratories-St Paul (SC)
for the treatment of structural heart disease.
The Opportunity
We are recruiting for a Regulatory Affairs Specialist II to join our team on-site in St. Paul, MN.As an individual contributor, the function of a Regulatory Affairs Specialist II is to provide support...
Kane Partners LLC-Malvern (PA)
Industry leader in manufacturing is seeking a Product Stewardship and Regulatory Affairs Specialist to manage product stewardship activities for promotion of new product and monitor compliance for existing portfolio at their state-of-the-art...
mindmatch.ai -
Abbott Laboratories-Alameda (CA)
working mothers, female executives, and scientists
This Senior Regulatory Affairs Specialist will work on-site out of our Alameda, CA or Milpitas, CA locations in the Diabetes Care Division. We’re focused on helping people with diabetes manage...
Katalyst Healthcares & Life Sciences-Pleasanton (CA)
Responsibilities:
As an experienced individual contributor, a Principal Regulatory Affairs Specialist is to provide support for the regulatory department, ensuring efficient and compliant business processes and environment.
This position performs...
resume-library.com -
Biolink360-San Francisco
Senior Regulatory Affairs Specialist - Remote Based - West Coast
Reports to: Global Regulatory Affairs Director
Salary Range: 140-170K
Location: Remote Based
Travel: Occasional travel to West Coast, must reside in Pacific or Mountain time zone...
appcast.io -
Katalyst Healthcares & Life Sciences-Gaithersburg
Responsibilities:
The Sr. Regulatory Affairs Specialist will prepare comprehensive regulatory strategies for complex new devices and post market changes within our Ultrasound business.
Serve as RA Representative on project teams, develops...
resume-library.com -
Abbott Laboratories-Atlanta
companies in the world by Fortune
• A company that is recognized as one of the best big companies to work for as well as a best place to work for diversity, working mothers, female executives, and scientists
This Regulatory Affairs Specialist II will work...
jobs.abbott -
Redwood City
patient needs in order to improve outcomes and quality of life for patients.
Job Summary & Responsibilities:
The Senior Regulatory Affairs Specialist is responsible for developing strategies for global approvals to introduce new Spinal cord stimulation...
icims.com -
Abbott Laboratories-Pleasanton (CA)
and scientists
The Opportunity
We are seeking a Principal Regulatory Affairs Specialist to join Abbott’s Heart Failure Division on-site in Pleasanton, CA.
As an experienced individual contributor, a Principal Regulatory Affairs Specialist is to provide support...
BioTalent-Worcester
Position Summary:
We are partnered with a class II device manufacturer to seek a Senior Regulatory Affairs Specialist to join their team. This is a hybrid opportunity to work on next-gen technology in the medical device space. Keys for this role...
mindmatch.ai -
Lifelancer-Thousand Oaks
Job Title: Senior Regulatory Affairs Specialist (USA - Remote)
Job Location: Thousand Oaks, CA, USA
Job Location Type: Remote
Job Contract Type: Full-time
Job Seniority Level: Mid-Senior level
Employer Industry: Medical Device Manufacturing...
resume-library.com -
Proteintech Group-Rosemont (IL)
We are seeking an experienced Quality Assurance and Regulatory Affairs Specialist to join our team. The ideal candidate will have a strong background in ISO 13485 quality management systems and experience with the registration of ASRs (Analyte...
mindmatch.ai -
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