- Merck & Co. (Rahway, NJ)
- …& Technology (DD&T) organization designs, develops, and commercializes novel biologic/ drug / vaccine - device enabled combination products to achieve safe and ... methods, and robust manufacturing processes for both clinical and commercial use . This position interacts extensively with subject-matter experts within the broader… more
- Merck & Co. (San Francisco, CA)
- …of DSCS Digital initiatives.Development Sciences and Clinical Supply (DSCS) enables Drug Substance, Drug Product, Analytical Development, and Clinical Supply ... responsible for implementing improved project management methodologies across DSCS Digital use -cases. The ideal candidate should have strong project management and… 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
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …and validations of R package and/or shiny apps. Identify and build the use cases and process/resources to guide the implementations. Lead, advocate and nurture R ... on R capabilities and systems: Collaborate with RD non-BDM and non-RD R user group or developers. Collaborate with biostat innovation to enhance BDM overall R… more
- Merck & Co. (Rahway, NJ)
- …scale-up, Drug Delivery and/or technology transfer experience including the use of gap analysis and risk assessment toolsHighly motivated, flexible, a change ... team is responsible for the research and development of sterile & parenteral drug products for biologics, Antibody Drug Conjugates and Small Molecules, including… more
- Merck & Co. (Rahway, NJ)
- …establish a consolidated , visible forecast for all study product needs (Bulk Drug Product and Clinical Finished Goods).- - Responsible for authoring clinical supply ... activities. - Participate in Interactive Voice Response (IVR) System d evelopment and User Acceptance Testing (UAT) for assigned studies . - Mentors new team members… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …development, modeling, and deployment in MESCoordinate with other departments to gather user requirements, guage effort, and deliver robust, right first time EBR ... 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)
- …approve periodic review documentation for qualified equipment/systems (audit trails, user groups, system administration)Provide expertise and solutions to issues ... 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)
- …which support calibration interval extensionPartner with stakeholders assist in defining user requirements for new instrumentsResponsible for working with groups to ... salary or other discretionary compensation at any time based on individual, team, performance, or market conditions.Legend Biotech maintains a drug -free workplace. 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
- Aequor (Bothell, WA)
- …for the Associate Scientist are associated with supporting formulation and drug product development for a molecule preparing for commercialization. Role ... in formulation development work and to support analytical testing of antibody- drug conjugate molecules. Support analytical testing team by performing compendial… more
- Aequor (East Syracuse, NY)
- …used in the testing and characterization of raw materials, excipients, in-process, drug substance, and drug product samples including HPLC/UPLC methods and ... high temperature liquids and solids may also be handled. Use of a respirator may be required.Frequent repeated motions...of raw materials, excipients, biologics and other modalities in-process, drug substance, and drug product samples. The… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …Diagnostic Development Teams) and to external diagnostic business partners specifically: Use of CTA/CDx within clinical trialsDevice protocols and SAPsDevice ... (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
- ACROBiosystems Inc. (New York, NY)
- …and manufacturing recombinant proteins and critical reagents/assays to support drug development and clinical applications from target discovery and validation, ... candidate drug screening and optimization, CMC development, preclinical and clinical...and provide all-around support to our customers. You will use existing knowledge and continue to build familiarity of… 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)
- …data standard deliverables for world-wide regulatory application submissions of drug and vaccine clinical development projects. Accountability predominantly includes ... (FDA, EMA, PMDA),Guiding project teams preparing submission deliverables including use of Pinnacle 21 Enterprise,Up-versioning activities to specific versions of… more
- AUROBINDO (Dayton, OH)
- …Scientist with previous industrial experience developing and filing generic drug dosage forms (orals/liquids)Ability to develop the product using FBD, ... of Senior Scientist Formulation development and process developmentExperience in the generic drug industry with ANDA filing experience.Must have ability to work in a… more
- Novo Nordisk Inc. (Langhorne, PA)
- …conditions such as obesity, growth hormone-related disorders and rare bleeding disorders. We use our skills, dedication and ambition to help people with diabetes and ... home office personnel. Essential Functions Adhere to the Prescription Drug Marketing Act of 1987 and all related Novo...and all related Novo Nordisk policies regarding the judicious use of physician samples and stock items Ensure timely… more
- Aequor (Pearl River, LA)
- …procedures and within safety guidelines in the production of Flublok Drug Substance in the downstream processing (Clarification and Purification) and buffer ... lines, ancillary equipment (tube welders, tube sealers, peristaltic pumps), use of water-for-injection (WFI) point of use ...pumps), use of water-for-injection (WFI) point of use taps, etc. Activities will include executing techniques such… more
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