Regulatory Affairs Jobs in New Jersey
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Search Results - Regulatory Affairs Jobs in New Jersey
The Judge GroupWarren (NJ)
Summary:
The Director, Global Regulatory Affairs is responsible for contributing to the development and execution of regulatory strategies and managing regulatory submissions for company’s products. This role involves collaborating with cross...
Takeda PharmaceuticalCambridge
Affairs CMC Devices and Drug-Device Combination Product, you will provide strategic leadership and development to global regulatory subject matter experts to ensure innovative and robust regulatory strategies for medical devices and drug-device combination...
HUTCHMEDFlorham Park
PRIMARY FUNCTION
The Senior Director/Executive Director, Regulatory Affairs role will establish Regulatory Affairs function within HUTCHMED International. He or She will support the global product team in the development of sound global...
Takeda PharmaceuticalCambridge
Affairs CMC Devices and Drug-Device Combination Product, you will provide strategic leadership and development to global regulatory subject matter experts to ensure innovative and robust regulatory strategies for medical devices and drug-device combination...
GForce Life SciencesPlainsboro
Regulatory Affairs Labeling Operations Specialist
12. month Contract
Onsite in Plainsboro, NJ
Must be able to work on a W2
Job Description:
We are seeking a dynamic and experienced Regulatory Affairs Labeling Operations Specialist (Contractor...
Takeda PharmaceuticalCambridge
Affairs CMC Early Development you will provide strategic leadership and development to global CMC regulatory subject matter experts to ensure innovative, robust, fit-for-phase regulatory strategies for small molecule and biologic products for FIH to pre...
Clinical Dynamix, Inc.Bridgewater (NJ)jobvertise.com
Regulatory Affairs Manager Job Description
Overview
Manage Companys Regulatory Affairs for assigned products for US and Canada, including implementation of the overall regulatory strategy, preparation of regulatory submissions and interface...
Madison (NJ)pharmiweb.jobs
continuous improvement, innovation and appropriate risk taking.
• Demonstrates resilience and perseverance.
Degree / Experience Requirements
• Solid scientific background, Ph.D., M.D., PharmD, MS, or BS
• Significant experience in regulatory affairs (e.g...
Takeda PharmaceuticalCambridge
Affairs CMC Early Development you will provide strategic leadership and development to global CMC regulatory subject matter experts to ensure innovative, robust, fit-for-phase regulatory strategies for small molecule and biologic products for FIH to pre...
Prinston Pharmaceutical Inc.Somerset (NJ)
Affairs Director to lead our complex portfolio, including Biosimilars (351(k)) and 505(b)(2) innovative products. The Director will serve as the primary architect of regulatory strategy, navigating the evolving FDA landscape to ensure successful product...
Takeda PharmaceuticalCambridge
therapies to patients. By focusing R&D efforts on four therapeutic areas and other targeted investments, we push the boundaries of what is possible in order to bring life-changing therapies to patients worldwide.
This role is within the Global Regulatory...
Cranburyicims.com
equity participation, 401(k) matching, and excellent health benefits.
Position Summary:
Rocket Pharma is seeking a Director, Regulatory Affairs – CMC (Chemistry, Manufacturing, and Controls to support the success of our gene therapy programs by serving...
Made ScientificPrinceton (NJ)
for advanced therapies.
• Collaborate with Regulatory Affairs and the PMO to translate evolving regulatory and client expectations into actionable inspection readiness strategies, standards, and best practices.
Regulatory Inspections, Client Audits & Customer...
Net2Source (N2S)Rahway
will work closely with the PaCES lead to collaborate with individuals from Clinical Research, Regulatory Affairs, Biostatistics, Outcomes Research, and Operations to ensure COA endpoint strategies are consistent with and executed and interpreted to support...
esrhealthcareRahwayjobvertise.com
Job Location: Rahway NJ 07065
Onsite Requirements:
CMC experience or R & D experience preparing the reports that feed into the CMC section (a quality background could be transferrable)
Experience authoring technical reports and regulatory...
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