- 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
- Tris Pharma (Monmouth Junction, NJ)
- …method development and supports laboratory investigations and performance of non -routine testing such as method comparisons and evaluations.ESSENTIAL FUNCTIONS ... with test analysesExecutes designed studies to support laboratory investigationsPerforms non -routine testing such as method comparisons and evaluationsDocuments all… 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
- Washington VA Medical Center (Washington, DC)
- …pursuant to Executive Order 12564; Reasonable suspicion testing is authorized in non - drug testing designated positions; All applicants tentatively selected for ... limited to: Perform at a competent level and work collaboratively in the Non -VA Care Coordination coordinated care delivery model, specifically in support of the… more
- Tris Pharma (Monmouth Junction, NJ)
- …developments in analytical chemistry, physical characterization and pharmaceutical testingPrepares non -conformance, Out of Trend (OOT), Out of Specification (OOS) ... GC-MS, ICP-MS, TLC and dissolution apparatusWorking knowledge of cGMP, Food and Drug Administration (FDA), Drug Enforcement Administration (DEA) and Occupational… 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
- 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
- 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
- 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
- Legend Biotech USA, Inc. (Raritan, NJ)
- …according to cGMP requirements.Lead a ~250+ organization responsible for either the non -sterile or sterile manufacturing processes in a 24/7 operation and be ... salary or other discretionary compensation at any time based on individual, team, performance, or market conditions.Legend Biotech maintains a drug -free workplace. 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
- 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
- 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
- Elanco Animal Health Incorporated (Indianapolis, IN)
- …assessment principles aligned with global regulations and guidance. Experience in non -clinical veterinary drug development, including target safety assessments, ... life better - join our team today! Your Role: Senior Research Scientist, Non -Clinical Safety & Toxicology We are seeking an experienced non -clinical toxicology… 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
