- Merck & Co. (Rahway, NJ)
- Job Description Job Description: - The drug development Project Manager is part of Global Project and Alliance Management (GPAM) which sits in the Research & ... Director, Project Manager, is a core member of Early Drug Development and/or Late Drug Development Teams,...Using these tools to integrate activities across key team members , proactively identify risks, and ensure clear and effective… more
- Merck & Co. (Rahway, NJ)
- …designing, developing and scaling-up the formulation, device, and manufacturing process.- Driving drug product design from the bench top to the Good Manufacturing ... facilities, our Scientists use cutting edge science to transform drug delivery and manufacturing technology to positively impact patients.The successful… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …responsible for performing a wide range of activities to support the release of drug products for human use. This position is responsible for quality and maintaining ... procedures, and all applicable regulations.Key Responsibilities Manage the team responsible for drug product batch record review and drug product release… more
- Merck & Co. (Rahway, NJ)
- …solving complex problems. Experience in one or more of the areas of Drug Substance development, Drug Product development, Clinical Supply management or ... our operations is desirable. Development Sciences and Clinical Supply (DSCS) enables Drug Substance, Drug Product, Analytical Development, and Clinical Supply… more
- Tris Pharma (Monmouth Junction, NJ)
- …science and technology.Our science and technology make us unique, but it is our team members that set us apart; they are the engine that fuels Tris' passion and ... projects. The incumbent ensures thorough characterization of formulations and drug delivery technologies under development and builds in-house analytical… more
- Merck & Co. (Rahway, NJ)
- …of the Program Lead, you will collaborate with global, cross-functional team members including clinical directors and study managers to lead/support clinical trial ... the Clinical Director.Builds talent and capabilities of direct/indirect team members through proactive coaching, mentoring and development opportunities.May include… more
- Merck & Co. (South San Francisco, CA)
- …Company's investments in human genetics and other multimodal data to support drug discovery in the cardiometabolic disease space.- Your work will inform discovery, ... aligning resources based on scientific priorities, and mentoring and developing team members . You will operate in a highly collaborative environment, partnering with… more
- Merck & Co. (Rahway, NJ)
- …biopharmaceutical company.- Our Research Division drives breakthrough science through drug discovery, development and clinical evaluation that radically changes ... spending.- The incumbent is also responsible for developing, coaching, and managing team members to meet both business and individual goals.Under the guidance of the… 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 ... a strong focus on supporting a CRO, CMO, or drug development organization. Working knowledge of selling GMP CMC...of competitor's offeringsServe as a mentor for other team members in support of their goalsIdentify, lead, and/or actively… more
- Merck & Co. (Rahway, NJ)
- …(FLEx) Center is a new multi-modality (small molecule, biologics, vaccine) Drug Product development and clinical manufacturing facility in Rahway, New Jersey.- ... fills, and autoinjector assembly. This team produces clinical and development drug product batches in a GMP piloting facility supporting our research… more
- Legend Biotech USA, Inc. (Raleigh, NC)
- …customer needs and achieve corporate goals.Works cooperatively with internal team members on various cross-functional projects related to specific accounts or ... in a timely manner, submitting expenses, etc.Reports adverse events to Legend's Drug Safety department and other internal departments as appropriate per required… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …with CROs and other vendors to ensure high quality deliverables to support drug development processes and global submissions as required for clinical trials. These ... SAS programs for clinical trials. This position will work closely with other members of the Biostatistics and Data Management teams on various clinical projects and… more
- Merck & Co. (Rahway, NJ)
- …team is responsible for the research and development of sterile & parenteral drug products for biologics as well as the biopharmaceutics support for the oral ... impactProactively identify key biopharmaceutics risks at each stage of drug product development for small molecules and/or biologics, conducting hypothesis-based… more
- Merck & Co. (Minneapolis, MN)
- …driven to succeed! Our Oncology Sales Representatives / Specialists serve as key members of our customer facing organization and partner with customers to address ... in a complex buying environment. This includes the multiple channels of drug distribution, Oncology GPO's, wholesalers and specialty pharmacies. Review and evaluate… more
- Exela Pharma Sciences, LLC (Lenoir, NC)
- …corporate policies, and the regulatory requirements of the US Food and Drug Administration. Job Responsibilities: Comply with garbing and behavior requirements that ... completion of finishing batch records and paperworkEnsure self and finishing team members are trained and work in compliance with applicable SOPs, cGMPs, regulatory… more
- Tris Pharma (Monmouth Junction, NJ)
- …science and technology.Our science and technology make us unique, but it is our team members that set us apart; they are the engine that fuels Tris' passion and ... Procedures (SOPs), current Good Manufacturing Practices (cGMPs) and Food and Drug Administration (FDA) standards. Performs routine and complex work related to… more
- Tris Pharma (Monmouth Junction, NJ)
- …and technology. Our science and technology make us unique, but it is our team members that set us apart; they are the engine that fuels Tris' passion and innovation. ... Procedures (SOPs), current Good Manufacturing Practices (cGMPs), Food and Drug Administration (FDA) standards and batch record specifications.The incumbent uses… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …R&D etc.); conducting risk assessments; and ensuring accountability of team members for deliverables. Additionally, the Risk Assessment lead will communicate across ... on action items between team meetings and ensure accountability of team members .Interface with all levels of management and ensure alignment throughout the… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …overall program safety reporting (eg, Periodic Safety Update Reports (PSURs), Drug Safety Update Reports (DSURs), and other safety-related documents, in ... relevant DSI stakeholders on the disease area, competitive landscape, and compound/ drug . May serve as speaker for program/ franchise medical/scientific training in… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …space including but not limited to clinical trial management system, drug labeling, and learning management system.Administration of enterprise job scheduler, Manage ... operational issues. Track problems and incidents and document status from team members and communicate status and system performance to management. Serve as… more
