- Daiichi Sankyo, Inc. (Bernards, NJ)
- …rare diseases and immune disorders. This position will be supporting early clinical safety for our Rare Disease/Specialty Medicine portfolio. SummaryThe Director, ... Safety, will be a product safety lead or part of a product safety team, and be responsible...and provide safety leadership including but not limited to clinical studies, post-marketing surveillance, signal detection and management, important… more
- Merck & Co. (Rahway, NJ)
- …of preclinical discovery into compounds ready for assessment in large clinical populations.We are seeking a highly qualified physician-scientist with a proven ... 5-year experience in the pharmaceutical industry and Immunology R&D and clinical and academic expertise in Immunology-related areas such as Dermatology,… more
- Merck & Co. (Rahway, NJ)
- …biologics, vaccine) Drug Product development and Good Manufacturing Practice (GMP) clinical supply manufacturing facility in Rahway, New Jersey.The Sterile Process ... and communication skillsets to drive the success of our clinical manufacturing facility and organization. As the facility is...Off-shift (2nd) work will intermittently be expected as a part of the role to support operations areas. The… more
- Merck & Co. (Rahway, NJ)
- …ability to successfully participate in and lead cross-functional teams is a critical part of this role. The Executive Director has scientific and budgetary oversight ... resource utilization and costs, physician and patient satisfaction surveys, clinical and patient reported outcomes assessments, systematic reviews and meta-analyses,… more
- Merck & Co. (Rahway, NJ)
- …Senior Engineer in Device Design and Process Development group, you will be part of our Research & Development team that designs and develops benchtop/low-volume to ... high-volume clinical and commercial assembly equipment and processes for medical...Working knowledge of regulatory requirements and standards (21 CFR Part 4, 21 CFR Part 820, ISO… more
- Formation Bio (New York, NY)
- …candidate drugs than the industry can progress because of the high cost and time of clinical trials. Recognizing that this development bottleneck may ultimately ... capabilities to accelerate all aspects of drug development and clinical trials. Formation Bio partners, acquires, or in-licenses drugs...values, and every team and individual plays a key part in our mission to bring new treatments to… more
- Formation Bio (New York, NY)
- …candidate drugs than the industry can progress because of the high cost and time of clinical trials. Recognizing that this development bottleneck may ultimately ... capabilities to accelerate all aspects of drug development and clinical trials. Formation Bio partners, acquires, or in-licenses drugs...values, and every team and individual plays a key part in our mission to bring new treatments to… more
- Formation Bio (New York, NY)
- …candidate drugs than the industry can progress because of the high cost and time of clinical trials. Recognizing that this development bottleneck may ultimately ... capabilities to accelerate all aspects of drug development and clinical trials. Formation Bio partners, acquires, or in-licenses drugs...values, and every team and individual plays a key part in our mission to bring new treatments to… more
- Formation Bio (New York, NY)
- …candidate drugs than the industry can progress because of the high cost and time of clinical trials. Recognizing that this development bottleneck may ultimately ... capabilities to accelerate all aspects of drug development and clinical trials. Formation Bio partners, acquires, or in-licenses drugs...values, and every team and individual plays a key part in our mission to bring new treatments to… more
- Merck & Co. (Rahway, NJ)
- …interpersonal and problem-solving skills to join our Modeling and Informatics (M&I) team.As part of the Discovery Chemistry family, M&I employs state of the art ... on our discovery organization, from target identification through delivery of clinical candidates across our fast-growing peptide project portfolio. With in-house… more
- Formation Bio (New York, NY)
- …candidate drugs than the industry can progress because of the high cost and time of clinical trials. Recognizing that this development bottleneck may ultimately ... capabilities to accelerate all aspects of drug development and clinical trials. Formation Bio partners, acquires, or in-licenses drugs...values, and every team and individual plays a key part in our mission to bring new treatments to… more
- Formation Bio (New York, NY)
- …candidate drugs than the industry can progress because of the high cost and time of clinical trials. Recognizing that this development bottleneck may ultimately ... capabilities to accelerate all aspects of drug development and clinical trials. Formation Bio partners, acquires, or in-licenses drugs...values, and every team and individual plays a key part in our mission to bring new treatments to… more
- Formation Bio (New York, NY)
- …candidate drugs than the industry can progress because of the high cost and time of clinical trials. Recognizing that this development bottleneck may ultimately ... capabilities to accelerate all aspects of drug development and clinical trials. Formation Bio partners, acquires, or in-licenses drugs...values, and every team and individual plays a key part in our mission to bring new treatments to… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …the treatment of multiple myeloma.Legend Biotech is seeking Technical Trainer as part of the Technical Operations team based in Raritan, NJ. Role OverviewTechnical ... for performing training activities for Operations team members who support cGMP Clinical and Commercial Cell Therapy Manufacturing. This individual will partner with… more
- Daiichi Sankyo, Inc. (New York, NY)
- …hospitals, and community practices).Demonstrate understanding of current or pending clinical pathways in assigned accounts, and how they influence patient ... databases as instruments to achieve assigned goals.Submits completed reports on- time , and communicates matters that are relevant to the...also eligible for a company vehicle. Our benefits are part of what makes Daiichi Sankyo, Inc. a great… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …myeloma.Legend Biotech is seeking Operations Support Specialist, Sun-Wed 2nd Shift as part of the Technical Operations team based in Raritan, NJ. Role OverviewThe ... Operations Support Specialist will be part of the Technical Operations team responsible for the...production of a personalized cell therapy to support both clinical and commercial requirements in a sterile cGMP environment.… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …the treatment of multiple myeloma.Legend Biotech is seeking a Quality Systems Lead as part of the Quality team based in Raritan, NJ. Role OverviewThe Quality Systems ... systems processes within a cell therapy manufacturing facility to support both clinical and commercial requirements in a sterile GMP environment. This role will… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …treatment of multiple myeloma.Legend Biotech is seeking a Metrology Technician I/II as part of the Technical Operations team based in Raritan, NJ. Role OverviewThis ... position will be responsible for metrology support for cGMP Clinical and Commercial Cell Therapy Manufacturing. This individual will partner with various Technical… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …the treatment of multiple myeloma.Legend Biotech is seeking Maintenance Technician I as part of the Technical Operations team based in Raritan, NJ. Role OverviewThis ... for maintenance support and mechanical system operations for cGMP Clinical and Commercial Cell Therapy Manufacturing on a modified...after just three months of employment, and a paid time off policy that includes 15 vacation days, 5… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …treatment of multiple myeloma.Legend Biotech is seeking QA Validation Specialist III as part of the Quality team based in Raritan, NJ. Role OverviewThe QA Validation ... within a cell therapy manufacturing plant to support both clinical and commercial requirements in a sterile GMP environment....after just three months of employment, and a paid time off policy that includes 15 vacation days, 5… more
