Regulatory Jobs
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Senior Associate, Regulatory Operations/CMC
Title: Senior Associate of Regulatory Operations/CMCSummary:A leading, global pharmaceutical client of ours is looking to hire a Senior Associate of Regulatory Operations and CMC, based out of their New Jersey office. This rapidly growing client has drug products spanning generics, branded prescriptions, and injectables. This role will specifically...
Senior Regulatory Affairs Associate
Title: Senior Associate of Regulatory AffairsSummary: A leading, global pharmaceutical client of ours is looking to hire a Senior Associate of Regulatory Affairs, based out of their New Jersey office. This rapidly growing client has drug products spanning generics, branded prescriptions, and injectables. This role will specifically focus within the...
Regulatory Affairs Specialist
We have a current opportunity for a Regulatory Affairs Specialist on a contract basis. The Regulatory Affairs Consultant will be responsible for providing strategic guidance on regulatory requirements and submissions for medical devices. This role involves ensuring compliance with global regulations, preparing and managing regulatory submissions, a...
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Senior Regulatory Affairs Specialist
Summary:The Senior Regulatory Affairs Specialist is responsible for managing appropriate regulatory and technical information to ensure regulatory compliance and support product registrations globally. This individual must possess general knowledge of global regulatory requirements relative to regulated products and other areas of responsibility as...
Regulatory Affairs Specialist IVDR
We have a current opportunity for a Regulatory Affairs Specialist - IVDR on a contract basis in Northern Ireland. Please apply if you have the skill set and are interested:6-12 months projectFull time (39 hours per week)HybridStart - May/JuneIVDR Regulatory Knowledge, getting ready for clinical trials.GAP AssessmentsTechnical DocumentsIVDR submissi...
Regulatory Affairs Specialist IVDR
We have a current opportunity for a Regulatory Affairs Specialist - IVDR on a contract basis in Northern Ireland. Please apply if you have the skill set and are interested:6-12 months projectFull time (39 hours per week)HybridStart - May/JuneIVDR Regulatory Knowledge, getting ready for clinical trials.GAP AssessmentsTechnical DocumentsIVDR submissi...