- Merck & Co. (North Wales, PA)
- …Summary This position drives scientific planning, strategy and execution of Phase 1-4 clinical studies. Under the direction of the Program Lead, you will collaborate ... with global, cross-functional team members including clinical directors and study managers to lead/support- clinical trial scientific activities.Job… more
- Merck & Co. (Rahway, NJ)
- …characterization groupsLeads project activities at external manufacturing sitesFacilitate manufacturing , packaging and release of clinical supplies for ... Job DescriptionOur company's Pharmaceutical Sciences & Clinical Supplies organization translates molecules to medicines, working from the discovery interface through… more
- Merck & Co. (Rahway, NJ)
- …To achieve this, we work closely with colleagues in Discovery, Pre- clinical , Early Development, Analytical, Formulation, and Commercial Manufacturing while ... development of innovative and disruptive technologies for next-generation biologic manufacturing processesDevelop and characterize robust clinical processes… more
- Catalent (Manassas, VA)
- Associate Director, Regulatory Affairs Position Summary: Catalent is a global, high-growth, public company, and a leading partner for the pharmaceutical industry in ... the development and manufacturing of new treatments for patients worldwide. Your talents,...consumer and Catalent employee. The primary duty of the Associate Director, Regulatory Affairs is to support regulatory strategy… more
- Merck & Co. (Rahway, NJ)
- …of our Research & Development Division is seeking applicants for an Associate Principal Scientist position available at its Kenilworth, New Jersey research ... facility.- The Associate Principal Scientist is a laboratory-based scientific role tasked with solving complex analytical problems at the interface of biology,… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …projects. Serve as the main interface to internal and external manufacturing sites. Review technical documentation (protocols, reports) associated with ... Mgmt. (mAb, Drug Substance, Drug Product, or New Modality) perspective. Support technical recommendations for future manufacturing sites and their selections.… more
- Merck & Co. (North Wales, PA)
- …methodologies and tools to enable the discovery, development, regulatory approval, manufacturing , and marketing of medical drugs and vaccines for the benefit ... collaborate to discover the next medical breakthrough.Position Description: The Associate Principal Scientist Statistical Programming leads the statistical programming… more
- Merck & Co. (Rahway, NJ)
- …as well as methods for the release and shelf-life assessment of clinical supplies under good manufacturing practice (GMP) settings.Author investigational new ... Scientist, Small Molecule Research & DevelopmentIn your role as Associate Principal Scientist, you will be part of a...You would also contribute towards regulatory submissions to enable clinical trials. Your main responsibilities, which are in no… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …immunotherapy in the treatment of multiple myeloma. Legend Biotech is seeking an Operations Associate (2nd Shift) as part of the Technical Operations team based ... in Raritan, NJ. Role Overview This position is responsible for performing manufacturing procedures and the execution of scheduled tasks within a CGMP environment.… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …an immunotherapy in the treatment of multiple myeloma. Legend Biotech is seeking a Sr. Associate OpEx Engineer as part of the Technical Operations team based in ... for providing operational excellence continuous improvement support to the cGMP Clinical and Commercial Cell Therapy Manufacturing plant. This individual… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …responsibilities for supporting the quality systems processes within a cell therapy manufacturing facility to support both clinical and commercial requirements ... working in an aseptic manufacturing facility, preferably in quality assurance, manufacturing compliance, clinical quality, or cell therapy. A minimum of 2… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …Raritan, NJ. Role Overview This position will be responsible for managing the technical transfer and clinical /commercial manufacture of cell therapy products in ... in the treatment of multiple myeloma. Legend Biotech is seeking a Senior Manager/ Associate Director, External Manufacture as part of the Global Manufacturing … more
- Merck & Co. (North Wales, PA)
- …methodologies and tools to enable the discovery, development, regulatory approval, manufacturing , and marketing of medical drugs and vaccines for the benefit ... statistical programming activities for multiple and/or late stage drug/vaccine clinical development projects. -Accountability predominantly includes the development and… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …Biotech is seeking an Operations Supervisor (2nd shift) as part of the Technical Operations team based in Raritan, NJ. Role Overview The Operations Supervisor is ... an exempt level position working within Technical Operations team, responsible for directing the daily production...production of a personalized cell therapy to support both clinical and commercial requirements in a sterile cGMP environment.… more
- Catalent (Philadelphia, PA)
- …and a leading partner for the pharmaceutical industry in the development and manufacturing of new treatments for patients worldwide. Your talents, ideas, and passion ... located in the Philadelphia area is Catalent's global Center of Excellence for Clinical Supply Packaging. Catalent offers GMP secondary packaging and clinical … more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …Facilities and Engineering, MS&T/Finance. Requirements High school diploma or GED required. Associate 's degree from a two-year college or technical school ... The CAR-T Facility Supervisor is an exempt level position working within Technical Operations team. This individual will be responsible for managing facility… more
- Novo Nordisk Inc. (Boulder, CO)
- About the Department The Boulder Site is home to the specialized technical operations/CMC team for oligonucleotides and RNAi therapeutics, continuing its legacy as ... the hub for all manufacturing -related activities for GalXC™ and GalXC-Plus™ investigational therapeutics developed from Novo Nordisk's acquisition of Dicerna… more
- Spectraforce Technologies Inc (Summit, NJ)
- …initiatives, etc. Education and Experience: Bachelor's degree or Associate / Medical Technical degree and 3 years of Manufacturing or Operations experience or ... Position: Manufacturing Associate Duration: 06 Months Location:...Knowledge of Basic mathematical skills General understanding of cGMPs Technical writing capability Proficient in MS Office applications Background… more
- Nesco Resource (Tucson, AZ)
- Research Associate I & IIOpen to New/Recent Graduates Location: ONSITE TucsonMedical/ Clinical Affairs categoryPharma Services Assay DevelopmentJOB ... INFORMATIONResponsible for conducting research, development and manufacturing laboratory experimentation and other scientific activities to support… more
- Arthrex (Naples, FL)
- …development and medical education. Currently, Arthrex is actively seeking a dedicated Associate Product Manager to spearhead and oversee initiatives in the Spine ... overall marketing, product strategy, research and development requirements, development, and manufacturing coordination for new and emerging products. Works on … more
