Bioinformatics Quality Documentation Lead
Denton, Texas
Quest Diagnostics Incorporated
Job Description The Bioinformatics Quality Management Lead is responsible for overseeing quality, compliance, and regulatory needs for bioinformatics operations in a clinical diagnostics lab under CAP/CLIA requirements. This role requires a...
13d
| Job Type | Full Time |
Pharmacy Specialist - Regulatory Affairs - Full Time - Elijah McCoy Detroit
Detroit, Michigan
Become part of Henry Ford Health as a full time Pharmacy Specialist - Regulatory Affairs, playing a key role in advancing system wide pharmacy compliance. This individual will serve as the enterprise expert for pharmacy regulatory affairs, ...
13d
| Job Type | Full Time |
FDA Associate - Regulation, Labeling & Marketing (Mid-Level)
Washington, D.C.
Venable LLP's FDA Group seeks a mid-level associate to join its nationally recognized Food & Drug Law practice in the Washington, D.C. office. Venable's Food & Drug Law Group advises leading companies across the food, dietary supplement, me...
13d
| Job Type | Full Time |
Newark, Delaware
About the Role We are looking for an experienced Regulatory Affairs Product Associate to join our team with the Aortic Business Group. In this role, you will plan, develop, and prepare regulatory strategies and coordinate regulatory plannin...
13d
| Job Type | Full Time |
East Hanover, New Jersey
Join us and celebrate the beauty of human experience. Create for happier, healthier lives, with love for nature. Together, with our customers, we deliver food innovations, craft inspired fragrances and develop beauty and wellbeing solutions...
14d
| Job Type | Full Time |
Principal Regulatory Affairs Specialist
Eden Prairie, Minnesota
Why Join Bracco Medical Technologies? We care as much about our employees as we do our patients. Our culture fosters a work environment where employees can thrive, be passionate and have fun along the way.Each member of the Bracco Medical T...
14d
| Job Type | Full Time |
Japanese Bilingual FDA Research & Regulatory Consultant
Torrance, California
Japanese Bilingual FDA Research & Regulatory Consultant Employment Type: Full-time Work Hours: 09:00 am - 6:00 pm (Flexible arrangements available) Work Location: Torrance, CA Job Overview A consulting firm is seeking a dedicated and biling...
14d
| Job Type | Full Time |
Regulatory Affairs Specialist (FDA/Medical Device)
Torrance, California
Job Title: Regulatory Affairs Specialist (FDA/Medical Device) Location: Torrance, CA Type: Full-time (On-site) Schedule: 9:00 AM - 6:00 PM (Offers flexibility in occasions for your needs to take care of your family members or academic commi...
14d
| Job Type | Full Time |
Regulatory Affairs Specialist II - Temporary
Fort Worth, Texas
Support the EU's In Vitro Diagnostic Regulation (IVDR) transition activities that will impact all Bio-Rad products currently CE Marked under the IVD Directive. Activities include preparation revision of technical files when needed, update l...
14d
| Job Type | Temporary |
RN Clinical Regulatory Compliance Specialist
Grand Rapids, Michigan
Corporate position that supports Greenville, Big Rapids, and Reed City Hospitals. This hybrid position requires 4+ days per week on site supporting the above hospitals with occasional travel to Grand Rapids. About Corewell Health Our new na...
15d
| Job Type | Full Time |