Senior Regulatory Affairs Specialist
Texas
Join us today and make a difference in people's lives! LivaNova is a global medical technology company built on nearly five decades of experience and a relentless commitment to improving the lives of patients around the world. Our advanced ...
9d
| Job Type | Full Time |
Data Integrity Compliance Lead
Kalamazoo, Michigan
States considered: Preferred Kalamazoo, MI/US Eastern Time Zone, Remote will be considered Role Description Position Overview The Veterinary Medicine Research and Development (VMRD) Data Integrity Compliance Lead will serve as the organizat...
10d
| Job Type | Full Time |
Lincoln, Nebraska
States considered: Zoetis is the world's largest Manufacturer and Supplier of Animal Pharmaceuticals. At Zoetis in Lincoln, NE, we manufacture high quality medicines for dogs, cats, and livestock. Our plant has been recognized as one of the...
10d
| Job Type | Full Time |
Data Integrity Compliance Lead
Detroit, Michigan
States considered: Preferred Kalamazoo, MI/US Eastern Time Zone, Remote will be considered Role Description Position Overview The Veterinary Medicine Research and Development (VMRD) Data Integrity Compliance Lead will serve as the organizat...
10d
| Job Type | Full Time |
Operational Quality Specialist / Madison, WI (On-Site)
Madison, Wisconsin
***Must possess extensive GCP experience and the ability to liaison cross-functionally*** As one of the largest Clinical Research Organizations in the world, we have four Early Phase Clinical Research Units in the UK and US. We are currentl...
10d
| Job Type | Full Time |
Senior Regulatory Affairs Specialist
New Brighton, Minnesota
Overview The Senior Regulatory Affairs Specialist plays a essential role in ensuring our products meet all necessary regulatory requirements, allowing us to bring them to market and improve patient outcomes. This position supports the RA ac...
11d
| Job Type | Full Time |
Regulatory Affairs Specialist II - Temporary
Irvine, California
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...
11d
| Job Type | Temporary |
Quality and Compliance Specialist
Jubilant Draxlmage Radiopharmacies Inc, dba Jubilant Radiopharma
Quality & Compliance Specialist - Radiopharmacy Focus Location:home-office Travel:Up to 30% across pharmacy locations and Jubilant sites Are you passionate about quality and compliance in the radiopharmaceutical space? Jubilant Radiopharmac...
11d
| Job Type | Full Time |
Associate Electronic Submission Specialist
Lake Zurich, Illinois
Job Summary The Associate Electronic Submissions Specialist is responsible for building and publishing electronic submissions to Drug, Biological, and Device Regulatory Agencies. This position will routinely collaborate with Regulatory Affa...
11d
| Job Type | Full Time |
Principal Specialist, Regulatory Affairs
Summit, New Jersey
Company Overview ImmunityBio, Inc. (NASDAQ: IBRX) is a commercial-stage biotechnology company developing cell and immunotherapy products that are designed to help strengthen each patient's natural immune system, potentially enabling it to o...
11d
| Job Type | Full Time |