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... regulatory affairs, R&D, or Manufacturing (CTD Module 3) • Superior oral and written ... other international regulatory requirements for drug product dossiers • Manage, compile, and ...
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International Regulatory Affairs Jobs
... regulatory affairs, R&D, or Manufacturing (CTD Module 3) • Superior oral and written ... other international regulatory requirements for drug product dossiers • Manage, compile, and ...
The position will also require application of domestic and international regulation to products ... Act as back up to Regulatory Affairs Specialist I and II in the collection and management of ...
We are looking for a Regulatory Affairs Specialist (title/level flexible) for one of our class III ... PMA experience and international experience are a big +, but not necessary. This position would be ...
Find your place at Pace® Join us as a CMC Regulatory Affairs Specialist, where you'll put your ... Knowledge of regulatory requirements, including International Council for Harmonization (ICH ...
The Regulatory Affairs Specialist - International works with the Regulatory Affairs and Engineering teams to ensure compliance with all regulatory requirements. P28 is a leader in the development and ...
Regulatory Affairs Assistant 18 - 28 Job Description: Maintain/assist with US State Pesticide ... FIFRA) and international (Canada PMRA) authorities as well as follow-up of the related ...
The Regulatory Affairs position works closely with coordinators, clinicians, and clinical trial ... We have an international reputation for our work and we provide outstanding access for patients to ...
The Regulatory Affairs Supervisors is responsible for the development and administration of ... Verification of International compliance data entered by RA Specialists to ensure integrity of the ...
Director of Regulatory Affairs (Medical Devices) We are looking for a Director, Regulatory Affairs ... They should have experience preparing and maintaining international product registrations, filing ...
Team with business unit Regulatory Affairs Specialists (RAS) and international regulatory staffs to provide regulatory support for new products. Work with RAS, engineers and technical experts to ...
The Regulatory Affairs and Quality Compliance Manager supports the execution of regulatory and ... National, International and State Licensing * Identify state, national, and international medical ...
Job Description International Regulatory Affairs Coordinator responsibilities include, but are not limited to, the following: * Under the direction of the Director of Regulatory Affairs and Quality ...
THE ROLE ReShape Lifesciences has a fantastic opportunity for a Senior Regulatory Affairs ... Directly communicate with the FDA, international regulatory agencies, Authorized representative(s ...
Represent Regulatory Affairs in decision-making and interdepartmental meetings related to domestic and international regulations * Participate in regulatory strategy planning and change management in ...
The Director of Regulatory Affairs - International will work with cross-functional department leadership to build and execute regulatory strategies across the globe. They will oversee regulatory ...
Represent regulatory affairs on engineering and R&D product development project teams to ensure all ... on international and domestic markets. * Assess regulatory impact of post-market changes on ...
A successful Global Regulatory Affairs Specialist satisfactorily performs these general categories ... international regulatory developments and identify opportunities and/or implications to the ...
RIVANNA is seeking a medical device Regulatory Affairs professional to contribute to our emerging ... Understanding of international complexities and ability to determine most efficient way to ...
S. and international regulatory requirements. The Regulatory Affairs Specialist provides direct Worldwide Regulatory support to lifecycle management and new product development/new product ...
Works with international counterparts to ensure product registrations are completed in a timely manner. * Support R&D team with regulatory questions and requests. * Assists, as necessary, with ...
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