Regulatory Affairs Specialist III

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...

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...

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 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 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...

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...

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 the moment of birth through every phase of life. Our mission is simple, yet powerful:...

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...

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...

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...

**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...

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...