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New SearchThe Regulatory Affairs Manager is responsible for managing the regulatory affairs department and functions to ensure regulatory compliance of quality management system. Duties ...
Summary SUMMARY: Plans, coordinates, monitors compliance with federal, state and local regulations; manages accreditation activities necessary for maintaining required accreditation; ...
Job Title: Regulatory Affairs Manager Duration: Permanent / Full Time / Direct Hire Location: Kansas City, MO 64105 (HYBRID) - Relocation Assistance would be offered Plus ...
Your Job The Product Safety & Regulatory Compliance Team is seeking a Regulatory Affairs Manager to join our team. This role will support the Koch Agronomic Services (KAS) ...
Our client is developing precision delivery platforms for the treatment of neurological and oncological disorders. They are seeking a Regulatory Affairs Manager (Contractor) ...
Regulatory Affairs Manager page is loaded Regulatory Affairs Manager Apply locations Chicago, IL time type Full time posted on Posted 2 Days Ago job requisition id JR25547 ...
Qualifications: degree or above in a relevant discipline required years of industrial experience in IVD or medical device FDA registration in Chinese preferred Tasks: and ...
Job Title Sr. Regulatory Affairs Manager Job Description Senior Regulatory Affairs Manager (U.S. Hub based location) The Senior Regulatory Affairs Manager will develop and ...
Innovation Center, 777 Forest Edge Dr, Vernon Hills, Illinois, United States of America Req #1712 Friday, May 3, 2024 Job Overview: The Regulatory Manager will be instrumental ...
The Regulatory Affairs Manager is responsible for coordinating the regulatory activities for projects including new products and life cycle management. This includes development ...
The Regulatory Affairs Manager promotes the consistent and proper application of international marine regulations, fulfilling International Association of Classification Societies ...
Regulatory Affairs Manager Make sure to read the full description below, and please apply immediately if you are confident you meet all the requirements. Reporting Reports ...
Pharvaris is a late-stage biotech company developing bradykinin B2 receptor antagonists for bradykinin-mediated diseases, with offices in Switzerland (Zug), the Netherlands ...
Description: This client is a radiopharmaceutical company that is developing new therapeutics. This person is going to manage a new NDA submission for them that they plan ...
Position Summary: The Regulatory Affairs Manager, East EMEA is mainly focused on registrations and compliance work for raw materials and finished products with a focus on ...
SUMMARY: Plans, coordinates, monitors compliance with federal, state and local regulations; manages accreditation activities necessary for maintaining required accreditation; ...
My client is a market leading biopharma, developing and manufacturing innovative biologic immunotherapies using best-in-class patented processes, driving a new way forward ...
At Univercells , we are on a mission to make health equally accessible to all. Through the combination of process development and engineering expertise, we create synergies ...
THE COMPANY: Formulated Solutions is redefining the Pharmaceutical and Self-Directed Consumer Healthcare CDMO experience through creativity and invention; delivering our world ...
19901 Nordhoff St, Northridge, CA 91324, USA Req #981 04 April 2024 K indeva is a leading global contract developer and manufacturer (CDMO) with delivery platform expertise ...
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