Regulatory Affairs Jobs in Jersey City
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Search Results - Regulatory Affairs Jobs in Jersey City
Daiichi Sankyo, Inc.-Jersey City
between the products. When goals are tactically misaligned or at risk for these assets, this leader will be responsible for bringing the issue and potential solutions to the Head of US Regulatory Affairs in conjunction with the assigned US RA strategist...
Daiichi Sankyo, Inc.-Jersey City
focused on providing novel therapies in oncology, as well as other research areas centered around rare diseases and immune disorders.
We are currently seeking a Regulatory Affairs Intern for summer 2025. This full-time position works for approximately...
mindmatch.ai -
Daiichi Sankyo, Inc.-Jersey City
Bachelor's Degree required
• Advanced degree (e.g., Masters, Pharm.D., Ph.D., MD, JD) preferred
Experience Qualifications
• 7 or More Years in the pharmaceutical industry
• 4 or More Years in regulatory affairs, NDA, sNDA, BLA filing to FDA
Travel...
Daiichi Sankyo, Inc.-Jersey City
industry experience required
• 4 or More Years of direct regulatory affairs experience, including US labeling experience required
• Experience with ex-US labeling (outside the US) preferred
Travel - Ability to travel up to 10%
Daiichi Sankyo, Inc...
mindmatch.ai -
Daiichi Sankyo, Inc.-Jersey City
discipline required
• Advanced degree (e.g., Masters, Pharm.D., Ph.D., MD, JD) preferred
Experience Qualifications
• 4 or More Years in the pharmaceutical industry preferred
• 1 or More Years in regulatory affairs required
• Experience in (s)NDA/BLA filing...
Tehk Recruitment Ltd-Jersey City
Director, Regulatory Affairs (FDA)
New Jersey
• New role to the business
• Individual Contributor role and strategic also
• The only role of its type in the local site / location
• Responsible for EVERYTHING to do with Regulatory Affairs...
jobvertise.com -
Daiichi Sankyo, Inc.-Jersey City
pharmaceutical experience including 5 years of experience within Regulatory Affairs
• Knowledge of IND, NDA/BLA submission experience
• Experience with regulatory submission strategy globally will be preferred but not required.
• Experience in providing...
Axiom Software Solutions Limited-Jersey City
compliance with company Standard Operating Procedures and regulatory agency regulations/guidance.
• Represents Regulatory Affairs on cross-functional project teams.
• Provide technical expertise to cross-functional teams on managing the lifecycle...
resume-library.com -
Daiichi Sankyo, Inc.-Jersey City
discipline required
• Advanced degree (e.g., Masters, Pharm.D., Ph.D., MD, JD) preferred
Experience Qualifications
• 4 or More Years in the pharmaceutical industry preferred
• 1 or More Years in regulatory affairs required
• Experience in (s)NDA/BLA filing...
Daiichi Sankyo, Inc.-Jersey City
of relevant pharmaceutical experience including 5 years of experience within Regulatory Affairs
• Knowledge of IND, NDA/BLA submission experience
• Experience with regulatory submission strategy globally will be preferred but not required.
• Experience...
Daiichi Sankyo, Inc.-Jersey City
between the products. When goals are tactically misaligned or at risk for these assets, this leader will be responsible for bringing the issue and potential solutions to the Head of US Regulatory Affairs in conjunction with the assigned US RA strategist...
AbbVie-Jersey City
Immunology
Interacts with and influences other cross functional departments (e.g. Toxicology, Pharmacokinetics, Business Development, Clinical and Regulatory Affairs), as needed, to ensure the successful development, design and implementation...
resume-library.com -
Daiichi Sankyo, Inc.-Jersey City
focused on providing novel therapies in oncology, as well as other research areas centered around rare diseases and immune disorders.
We are currently seeking a Regulatory Affairs Intern for summer 2025. This full-time position works for approximately...
Daiichi Sankyo, Inc.-Jersey City
centered around rare diseases and immune disorders.
Summary
This position serves as the Global Regulatory Affairs (GRA) Labeling Strategy expert to the Global Product Team (GPT) as an ad hoc member and independently provides strategic and operational...
Daiichi Sankyo, Inc.-Jersey City
pharmaceutical industry experience required
• 4 or More Years of direct regulatory affairs experience, including US labeling experience required
• Experience with ex-US labeling (outside the US) preferred
Travel - Ability to travel up to 10%
Daiichi Sankyo, Inc...
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