- Merck & Co. (Rahway, NJ)
- …in cell culture commercialization. The primary objective of the Biologics Drug Substance Commercialization (BDSC), Cell Culture Sciences department is to provide ... recommends schedule changes, cost adjustments or resource additions.Solves technical and non -technical problems throughout the life of the project, tries to resolve… more
- Crinetics Pharmaceuticals (San Diego, CA)
- …the lives of others. Position Summary: The Vice President of Nonclinical Drug Safety and Toxicology is responsible for providing strategic and operational leadership ... experience. Preferred 10 years of experience managing and developing a drug safety/toxicology team. DABT certification strongly preferred. Experience in defining and… more
- Merck & Co. (Rahway, NJ)
- …is responsible for the research and development of sterile & parenteral drug products for biologics including monoclonal antibodies (mAbs), di- & tri-specific ... proteins as well as the biopharmaceutic support for the oral and non -oral portfolio. Within Biologics and Biopharmaceutics, the large molecule product development… more
- Merck & Co. (South San Francisco, CA)
- …on the discovery and development of small molecules, biologics and non -traditional therapeutics like peptides, novel biological constructs, and others. The Associate ... Director is a skilled quantitative drug developer, with a strong, integrated understanding of the...a strong, integrated understanding of the strategic elements of drug discovery and development. The Associate Director should demonstrate… more
- Merck & Co. (Rahway, NJ)
- …accountable for establishing the timelines for bulk manufacturing needs and release of drug product across assigned program(s) . - Works directly in the SAP system ... s used within the assigned program(s) ( ie Bulk Drug Product).- - Oversees all bulk drug ...of clinical supply chain metrics and/or participate in critical non -pipeline activities as a subject matter expert in a… more
- Gibson's Transportation (Johnson City, TN)
- Gibson Transportation is seeking Drivers for Non -Emergency Medical Transport in the Johnson City, TN area. DRIVER WANTED (NO EXPRIENCE NEEDED) to be a Tenn-Care ... transport for patients to and from doctor appointments. The non -emergency medical transport Driver plays a crucial role in...out. Qualifications Required: -Must be over 25 year's old - Drug & Background & Physical Check Are Required -Must… more
- Merck & Co. (Rahway, NJ)
- …manufacturing, packaging, and distribution- for our company development products and non -our company marketed products . - Analyzes and anticipates project risk ... establish a consolidated , visible forecast for all study product needs (Bulk Drug Product and Clinical Finished Goods).- - Responsible for authoring clinical supply… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …specifically:Use of CTA/CDx within clinical trialsDevice protocols and SAPsDevice non -significant/significant risk determinations (both submission to CDRH in a Q-sub ... (Dx) Partner to communicate key RA updates from the drug side, as needed. Provide RA specific inputs into...robust development of assay, participate in HA interaction for drug -related CDx topics/questions, and attend device company HA meetings… more
- Formation Bio (New York, NY)
- …is a tech and AI driven pharma company differentiated by radically more efficient drug development. Advancements in AI and drug discovery are creating more ... technology platforms, processes, and capabilities to accelerate all aspects of drug development and clinical trials. Formation Bio partners, acquires, or in-licenses… more
- Formation Bio (New York, NY)
- …is a tech and AI driven pharma company differentiated by radically more efficient drug development. Advancements in AI and drug discovery are creating more ... technology platforms, processes, and capabilities to accelerate all aspects of drug development and clinical trials. Formation Bio partners, acquires, or in-licenses… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …electrical devices, circuits, and switchgear used in cGMP and non GMP systemsInvestigate, troubleshoot, and provide repairs to equipment, instruments, ... local, state and federal regulations including and equivalent to Federal Drug Administration (FDA), Environmental Protection Agency (EPA), Occupational Safety and… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …Representing cross-functional collaborations on R capabilities and systems: Collaborate with RD non -BDM and non -RD R user group or developers. Collaborate with ... reporting of clinical trials. required- Having knowledge of all phases of drug development, including early and late phase clinical development and submission… more
- Merck & Co. (North Wales, PA)
- …as needed. More specifically,-Develops, coordinates, and provides biostatistical support for drug projects under the supervision of management.-Lead a team of staff ... recruiting and training other statisticians, providing statistical training for non -statistical groups, department research effort, and other committee works, etc.,… more
- Aequor (Pearl River, LA)
- …vaccines that matter most. Whether you are in the discovery sciences, ensuring drug safety and efficacy or supporting clinical trials, you will apply cutting edge ... Communicate complex data and results clearly to both technical and non -technical stakeholders. Collaborate extensively with those from other scientific disciplines… more
- Insmed Incorporated (San Diego, CA)
- …participate in the process execution within a Pilot Plant non -GMP manufacturing environment.Review batch records, SOPs, raw material specifications, protocols ... and business strategies.Facilitate collaboration with both internal and external drug substance analytical, quality control, quality assurance, and manufacturing… more
- Genmab (NJ)
- …are in scope.The Programming Manager will support the Data Management, Statistics, Drug Safety, Medical, Clinical Pharmacology and Biomarker functions with the above ... corresponding programs and ensuring QC before formal release, for the following non -comprehensive list of deliverables: IB, DSUR, briefing packages for FDA, EMA… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …improvements, optimization, capacity expansion, and cost of goods / non -conformance reduction efforts worldwide.Key Responsibilities Represent MSAT at joint ... salary or other discretionary compensation at any time based on individual, team, performance, or market conditions.Legend Biotech maintains a drug -free workplace. more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …the CAR-T Raritan SiteReview and approve change controls, SOPs, non -conformances, and CAPAs associated with qualification/validation execution and ensure ... salary or other discretionary compensation at any time based on individual, team, performance, or market conditions.Legend Biotech maintains a drug -free workplace. more
- Eisai, Inc (Nutley, NJ)
- …region and need dependent; does not include USMA).Provide additional non -didactic and soft-skills training (eg medical insights workshops, presentation skills, ... desired therapeutic area(s); comfortable and confident speaking about multiple drug indications/disease state management and competitor products and data.Understanding… more
- Merck & Co. (Rahway, NJ)
- …for clinical trial decision-making, regulatory requests, clinical study reports, and new drug application filing. Produce SAS data transport files and program text ... have an interest and ability to work in an exploratory environment, handling non -standard data in a variety of formats with minimal requirements; and an interest… more
