Regulatory Affairs Jobs in Cambridge
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Search Results - Regulatory Affairs Jobs in Cambridge
Sanofi-Cambridge
About the Role
The Associate Director, US Regulatory Affairs (RA) serves as the regulatory lead on relative Review Committees (RCs), for products in the Rare Disease, Rare Blood Disorder and Neurology portfolio. As the RC RA representative, work...
PSG Global Solutions-Cambridge
Description
We're looking for a Manager of Regulatory Affairs, working in Biotechnology/Medical Devices industry in Cambridge, Massachusetts, United States.
• Works with Regulatory Affairs management to define regulatory strategy and to compile...
appcast.io -
Sanofi-Cambridge
Global Regulatory Affairs Lead (GRL)
Mission statements
• The Global Regulatory Affairs Lead (GRL) is the fully accountable decision maker for the development & execution of creative, thoughtful, and robust global regulatory strategies...
The Fountain Group LLC-Cambridge
The Fountain Group are a national staffing firm and are currently seeking a Regulatory Affairs Manager III for a prominent Pharmaceutical client of ours. This position is Remote. Details for the position are as follows:
Job Description:
Pay: 75.00...
resume-library.com -
PSG Global Solutions-Cambridge
Description
We're looking for an Associate Director of Regulatory Affairs, working in Pharmaceuticals and Medical Products industry in Cambridge, Massachusetts, United States.
• Works proactively in a cross-functional organization to partner...
appcast.io -
Katalyst Healthcares & Life Sciences-Cambridge
Responsibilities:
Responsible to communicate new regulatory guidelines. Lead the strategic efforts in the interpretation of relevant and new quality guidelines to ensure that the current and phase appropriate requirements and standards are properly...
resume-library.com -
PSG Global Solutions-Cambridge
Description
We're looking for an Associate Director Regulatory Affairs CMC, working in Pharmaceuticals and Medical Products industry in Cambridge, Massachusetts, United States.
• Leads development and execution of robust global regulatory CMC...
appcast.io -
The Fountain Group LLC-Cambridge
be remote but the manager prefers a candidate local to Cambridge, MA as he would like for them to come into the office a few time a month.
This is a Heavy Data Migration role, candidates should have Knowledge of Regulatory, Publishing, or EDMS models...
resume-library.com -
ONO PHARMA USA-Cambridge
industry, along with demonstrated success as a PV, Regulatory Affairs organizational leader, able to lead, direct and develop member of the PV regulatory function. Knowledge and experience in US and EU regulations, PMDA, ICH guidelines, and understanding...
mindmatch.ai -
Sanofi-Cambridge
preferredAt least 6 years of prior pharmaceutical/biotechnology industry experience, including at least 4 years of relevant Regulatory Affairs experience (regionally and/or global) especially in development phaseExperience with clinical development of drugs...
Biogen-Cambridge
Job Description
About the role:
The Senior Director, Global Regulatory Strategy, Therapeutic Area Lead in Global Regulatory Affairs is responsible for the development of end-to-end US, Above-Country EU and Global regulatory strategies for assigned...
resume-library.com -
Takeda-Cambridge
evaluate and recommend implementation strategy.
As part of the Regulatory Affairs CMC team, you will report to the Executive Director and Head, CMC Regulatory Affairs – Pharmaceuticals.
How you will contribute:
• Leads the Early Development...
mindmatch.ai -
Sanofi-Cambridge
experience, including at least 4 years of relevant Regulatory Affairs experience (regionally and/or global) especially in development phaseDemonstrated experience with preparation of (s)BLA/(s)NDA/ MAA, INDs/CTAs, Health Authority meeting briefing documents...
Alnylam Pharmaceuticals-Cambridge
with expertise areas outside of Combination Products including Manufacturing, Quality Assurance, Partners, Vendors, and Regulatory Affairs to commercialize and maintain patient-centric Combination Products.
Key Responsibilities
• Contribute to Human Factors...
mindmatch.ai -
Takeda-Cambridge
success in meeting goals/objectives.
As part of the GRA CMC Pharmaceuticals, Oligonucleotides team, you will report to the Executive Director and Head, CMC Regulatory Affairs, Pharmaceuticals.
How you will contribute:
• Responsible for demonstrating...
mindmatch.ai -
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