USA-Regulatory Affairs Specialist Project Lead I

Job Title: Regulatory Affairs Specialist Project Lead I Location: Bridgewater, NJ (Fully Remote) Duration: Contract till October 2024 with the possibility of extension Job Overview The Regulatory Affairs Specialist Project Lead I will oversee and manage regulatory projects with a focus on US FDA Advisory Committee (ADCOM) preparation. Experience in...

Hello, My name is Shivaraj, and I am a Scientific Talent Acquisition Consultant with The Fountain Group. Currently I have an opening for a Regulatory Affairs Project Lead, fully remote . Detailsfor the positionare as follows Pay: $92 Fully Remote This role will be accountable for leading the development and execution of innovative and value-added global...

Hello, My name is Shivaraj, and I am a Scientific Talent Acquisition Consultant with The Fountain Group. Currently I have an opening for a Regulatory Affairs Project Lead, fully remote. Details for the position are as follows Pay: $92 Fully Remote This role will be accountable for leading the development and execution of innovative and value–added...

Regulatory Affairs Specialist Project Lead I (Scientific)REMOTE06 MonthsRequires candidates that have worked on medicinal products (small molecule or biologic) marketing applications-- like NDA, BLA, MAA.Description:This role will be accountable for leading the development and execution of innovative and value-added global regulatory strategies and be...

Hello, My name is Shivaraj, and I am a Scientific Talent Acquisition Consultant with The Fountain Group. Currently I have an opening for a Regulatory Affairs Project Lead, fully remoteDetails for the position are as follows Pay: $92 Fully Remote This role will be accountable for leading the development and execution of innovative and value-added global...

Regulatory Affairs Specialist Project Lead I Location: Bridgewater, NJ (Fully Remote) Duration: Contract till Oct 2024 with possibility to extend Fully Remote This role will require direct experience in US FDA Advisory Committee (ADCOM) Preparation. Experience in Immunology products is preferred, but any ADCOM experience will be considered. Education and...

Regulatory Affairs Specialist Project Lead I Location: Bridgewater, NJ (Fully Remote)Duration: Contract till Oct 2024 with possibility to extendFully RemoteThis role will require direct experience in US FDA Advisory Committee (ADCOM) Preparation. Experience in Immunology products is preferred, but any ADCOM experience will be considered.Education and...

Regulatory Affairs Specialist Project Lead I Location: Bridgewater, NJ (Fully Remote)Duration: Contract till Oct 2024 with possibility to extendFully RemoteThis role will require direct experience in US FDA Advisory Committee (ADCOM) Preparation. Experience in Immunology products is preferred, but any ADCOM experience will be considered.Education and...

Fully Remote This role will be accountable for leading the development and execution of innovative and value-added global regulatory strategies and be responsible for formulating the Global Regulatory Project Strategy (GRPS) for immunology products in Early Development. Additionally, this role leads the development of a global HA (Health Authority)...

Fully Remote This role will be accountable for leading the development and execution of innovative and value-added global regulatory strategies and be responsible for formulating the Global Regulatory Project Strategy (GRPS) for immunology products in Early Development. dditionally, this role leads the development of a global HA (Health Authority)...

Job Description: Pay Range: $87.41hr - $92.41hr Responsibilities: This role will be accountable for leading the development and execution of innovative and value-added global regulatory strategies and be responsible for formulating the Global Regulatory Project Strategy (GRPS) for immunology products in Early Development. dditionally, this role leads...

Description We're looking for a Regulatory Affairs Specialist III , working in Pharmaceuticals and Medical Products industry in Bridgewater, New Jersey, United States . Contributes to the development and oversees the successful implementation of regulatory strategies for assigned products, including submission and maintenance activities related to BLA...

Fully Remote This role will require direct experience in US FDA Advisory Committee (ADCOM) Preparation. Experience in Immunology products is preferred, but any ADCOM experience will be considered. Education and Experience: " BS/BA degree in a relevant scientific discipline required. Advanced degree (PharmD, PhD, MD or DVM or MSc in Biology, Life Science, or...

**Bausch + Lomb (NYSE/TSX**: BLCO) is a leading global eye health company dedicated to protecting and enhancing the gift of sight for millions of people around the world—from the moment of birth through every phase of life. Our mission is simple, yet powerful: helping you see better, to live better. Our comprehensive portfolio of over 400 products is...

Apply now and our proprietary system will quickly have you in front of a live recruiter. The Opportunity Description We're looking for a Regulatory Affairs Specialist III, working in Pharmaceuticals and Medical Products industry in Bridgewater, New Jersey, United States. Contributes to the development and oversees the successful implementation of...

Press Tab to Move to Skip to Content Link Select how often (in days) to receive an alert: Select how often (in days) to receive an alert: Senior Principal Regulatory Affairs Specialist Bausch + Lomb (NYSE/TSX: BLCO) is a leading global eye health company dedicated to protecting and enhancing the gift of sight for millions of people around the world—from...

Job title: CMC Regulatory Technical Writer II Location: Bridgewater, NJ, Hybrid Duration: 1 year SHIFT SCHEDULE 1st shift, 9-5 EST Mon-Fri Pay Rate starts: $47/ HOUR HM Notes: Hybrid - onsite Tuesday & Thursday - This can change at any time. 5 years experience with scientific background (BA/BS, MS or PhD) Must have experience with CTD (Common...

Job title: CMC Regulatory Technical Writer II Location: Bridgewater, NJ, Hybrid Duration: 1 year SHIFT SCHEDULE 1st shift, 9-5 EST Mon-Fri Pay Rate starts: $47/ HOUR HM Notes: Hybrid - onsite Tuesday & Thursday - This can change at any time. 5 years experience with scientific background (BA/BS, MS or PhD) Must have experience with CTD (Common...

Job title: CMC Regulatory Technical Writer II Location: Bridgewater, NJ, Hybrid Duration: 1 year SHIFT SCHEDULE 1st shift, 9-5 EST Mon-Fri Pay Rate starts: $47/ HOUR HM Notes: Hybrid - onsite Tuesday & Thursday - This can change at any time. 5 years experience with scientific background (BA/BS, MS or PhD) Must have experience with CTD (Common...

Regulatory Affairs Specialist (Hybrid) Kelly® Science & Clinical is seeking a Regulatory Affairs Specialist for our client in Bridgewater, New Jersey.  If you’re passionate about bringing the latest scientific discoveries to life and are ready to take the next step in your career, trust The Experts at Hiring Experts.This client is a company that’s...