- Aequor (Thousand Oaks, CA)
- …biotechnology companies, reaching over 10 million patients worldwide. Leverage your high- level expertise to lead and forge partnerships that advance the biotechnical ... more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …causality, and expectedness of the adverse event in relation to the drug . Ensure all relevant data and findings are incorporated into comprehensive safety ... more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …disorders. Summary This position is responsible for providing project management, drug development expertise to Global Project Teams including strategic development ... more
- Aequor (Bothell, WA)
- …you will be an active team member who influences at the project team level .You will be using your scientific judgment to adapt standard methods and techniques by ... more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …and partners to ensure high quality deliverables are on time to support drug development processes and global submissions. This position also partners with internal ... more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …NJ. Role OverviewThe Sr. Maintenance Specialist, Cleaning Services is an exempt level position working within Maintenance and Metrology team. This individual will be ... more
- Lovelace Biomedical Research Institute (Albuquerque, NM)
- …disciplines. Founded in 1947 as a not-for-profit corporation, LBRI employs ~35 PhD level scientists and ~250 technicians and staff. The Lovelace mission is to serve ... more
- Merck & Co. (Rahway, NJ)
- …capabilities across our organization's network. This includes NMR capabilities for drug discovery and process development across small molecules, biologics, and ... more
- BioAgilytix (San Diego, CA)
- …fast-paced, fun and never boring. Because we work across numerous clients and drug modalities, your career can develop rapidly. You'll gain experience with a variety ... more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …all cardiometabolic pipeline assets, early product management, opportunity and drug identification, early commercialization strategy, pipeline strategy and product ... more
- BioAgilytix (Boston, MA)
- …fast-paced, fun and never boring. Because we work across numerous clients and drug modalities, your career can develop rapidly. You'll gain experience with a variety ... more
- Legend Biotech USA, Inc. (Pittsburgh, PA)
- …in a timely manner, submitting expenses, etcReports adverse events to Legend's Drug Safety department and other internal departments as appropriate per required ... more
- Genmab (NJ)
- …maximize patient access and optimize profitability of Genmab products.Manage High level communications that will align brand with market dynamics and competitive ... more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …for his/her portfolio. Serves as the company's senior representative with key high- level internal and external stakeholders on important drug safety issues ... more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …to business users at our manufacturing site. This role involves providing Level 1 support for IT applications, assisting users with transactional issues, ... more
- Merck & Co. (Rahway, NJ)
- …Mechanical Coordinator include the following:The Mechanical Coordinator role at the Specialist level will serve as a team member supporting the Modality Agnostic ... more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …Practices (GCPs), appropriate Standard Operating Procedures (SOPs), Food and Drug Administration (FDA) regulations/EU Directive, and International Conference on ... more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …inventories supporting manufacturing activities to provide an optimal service level and performance.Key Responsibilities Interpret and analyze demand and usage ... more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …in Raritan, NJ. Role OverviewThe Quality Systems Lead role is an exempt level position with responsibilities for supporting the quality systems processes within a ... more
- Merck & Co. (North Wales, PA)
- …specification and intersection with IRT and clinical supplies.US and/or worldwide drug or vaccine regulatory application submission experience at the leadership ... more
