- Merck & Co. (North Wales, PA)
- Job DescriptionThe Senior Director , GCTO Project Management Office will report to the Executive Director , Head of the GCTO Project Management Office (PMO). ... Build and maintain strong relationships with key stakeholders, including senior leaders, business area contacts, and project teams. Effectively communicate… more
- Merck & Co. (North Wales, PA)
- …with talented and dedicated colleagues while developing and expanding your career.The Senior Clinical Director (Sr. Principal Scientist) has primary ... team. Our Company's Oncology medicines span all phases of clinical development (pre- clinical to post-licensure). The Senior Director will manage the… more
- Catalent (Harman, WV)
- Senior Director , Supply Chain Position Summary: The Senior Director , Supply Chain is responsible for leading the supply chain organization for Catalent ... Maryland. Catalent Maryland is a commercial Gene Therapy manufacturing facility with ten suites actively operating and eight...online.Reporting to the Vice President and General Manager, the Senior Director Supply Chain directs all facets… more
- Merck & Co. (Rahway, NJ)
- …technical and project management responsibility. The Senior Specialist - Manufacturing Automation position will report to the Director , Engineering, ... (small molecule, macrocyclic peptides, bioconjugates) Drug Substance development and GMP clinical manufacturing plant currently planned in Rahway, New Jersey.… more
- Merck & Co. (Rahway, NJ)
- …methodologies and tools to enable the discovery, development, regulatory approval, manufacturing , and marketing of medical drugs and vaccines for the benefit ... developing and coordinating statistical activities supporting drug/vaccine projects.Interacts with Clinical , Regulatory, Statistical Programming, Data Management, and our Company's… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …an immunotherapy in the treatment of multiple myeloma. Legend Biotech is seeking a Senior Manager/Associate Director , External Manufacture as part of the Global ... position will be responsible for managing the technical transfer and clinical /commercial manufacture of cell therapy products in our external manufacture… more
- Merck & Co. (South San Francisco, CA)
- Job DescriptionThe Executive Director of Cardiovascular (Cardio-renal disease & Heart Failure) will be responsible for overseeing and facilitating research in ... at a new state-of-the-art center in South San Francisco, CA. The Executive Director will contribute to the design, prioritization, and execution of the strategic… more
- Merck & Co. (Rahway, NJ)
- …our products is developed and realized. Role Summary: The Executive Director , Scientific Affairs (EDSA) maximizes meaningful bi-directional scientific exchange with ... the worldwide clinical and academic community to positively impact Research and Development (R&D) strategy for new medicines and to improve outcomes for patients.The… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionThe Executive Director of Global Marketing for HIV - Long-Acting Treatment Programs, will be at the forefront of driving our global commercial success ... HIV Long-Acting Treatment P rograms and gain a competitive advantage.Collaborate with Clinical Teams to shape the commercial HIV product profile, label, core claims… more
- Merck & Co. (North Wales, PA)
- …in commercialization, regulatory affairs, statistics, and manufacturing to manage clinical development projects; andAssist the Senior /Executive Director ... Our company's Oncology medicines span all phases of clinical development (pre- clinical to post-licensure). The Director will manage the entire cycle of… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionFLEx is a set of multi-modality Drug Product development and GMP clinical manufacturing assets being constructed in the Rahway, New Jersey site, ... to expense and capital expenditure.Defining and demonstrating operational excellence in a clinical manufacturing setting, across a spectrum of activities and… more
- Merck & Co. (Rahway, NJ)
- …on programs they lead to ensure high quality products and robust manufacturing processes.-- This position interacts extensively with subject-matter experts on the DD ... expected to apply his/her knowledge of product design and development; manufacturing process development, qualification, and validation; and, design control and risk… more
- Merck & Co. (South San Francisco, CA)
- Job DescriptionThe Director of Immuno-Metabolism will be responsible for overseeing and facilitating the research in metabolic disorders & inflammation, in the ... insights and complement internal pipeline.Monitor emerging biology and basic & clinical research within metabolic disorders & inflammation, and more broadly across… more
- Merck & Co. (Rahway, NJ)
- …of, contractors performing various GMP activities supporting the production of clinical supplies with focus on drug product. Additionally, experience in medical ... requirements across stakeholders.- Reviews draft policy and standards.Communicates with senior management within our Company and the contractor organization.-… more
- Merck & Co. (Rahway, NJ)
- Job Description Position Description: Director , Business Development - Enabling Technologies Search and Evaluation Job The Search and Evaluation (S&E) team is a core ... in-depth understanding of the underlying science behind each opportunity. The Director , Business Development & Licensing - Enabling Technologies Search and… more
- Catalent (Manassas, VA)
- Senior Quality Auditor 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,...safety of every patient, consumer and Catalent employee. The Senior Quality Auditor will be responsible for performing supplier… more
- Merck & Co. (Rahway, NJ)
- …to advance the drug discovery and development pipeline.We are seeking a Senior Information Architect with expertise in biopharma research to support our ... biopharma research, such as public Omics databases (eg, GenBank, GEO), clinical trial repositories (eg, ClinicalTrials.gov), patient-level data platforms (eg, OMOP,… more
- Insmed Incorporated (Bridgewater, NJ)
- …Best Workplaces in New York™, and Best Workplaces for Millennials™ lists.OverviewThe Director , Toxicology, is a key member of the nonclinical safety team, reporting ... to the Executive Director , Head of Toxicology and Molecular Mechanisms. In this...collaborating with subject matter experts in discovery, bioanalysis, pharmacokinetics, clinical development, CMC, and program management to drive the… more
- Merck & Co. (Rahway, NJ)
- …existing and pipeline products to produce safe, effective, innovative medicine.The Global Clinical Data Standards Vocabulary Specialist, Associate Director , is a ... Job DescriptionOur Clinical Research and Pharmacovigilance team push the boundaries...across GCDS by actively communicating and proactively sharing informationSupport senior /leadership roles, in areas of observed competence, to enhance… more
- Novo Nordisk Inc. (Boulder, CO)
- …RNAi therapeutics, continuing its legacy as the hub for all manufacturing -related activities for GalXC™ and GalXC-Plus™ investigational therapeutics developed from ... and is one of the world's leading centers for oligonucleotide innovation and manufacturing . Together, we are driving change. Are you ready to make a difference?… more
