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Develop, implement and manage Urovant’s quality systems and operations ensuring compliance with GCP, GVP, GMP and GLP.
We are seeking an Associate Director of Regulatory Affairs to play a critical role in the advancement of our pre-clinical and clinical programs.
Regulatory Affairs Manager plays a critical role in developing and managing Investigational New Drug (IND) submissions.
Our medical device client is seeking a Junior Regulatory Affairs Specialist! You'll be responsible for developing and influencing regulatory policy.
Our client, a Medical Device company is seeking a Regulatory Affairs Specialist to join their team!