- Merck & Co. (Rahway, NJ)
- …standards for new or modified processes.--Initiates and provides resources for technical support of capital projects in area of process, equipment, and/or automation ... Systems, plus a minimum of 5 years of related technical support or manufacturing automation experience or acceptable related experience.-Required Experience and… more
- Merck & Co. (Rahway, NJ)
- …internal network of subject matter experts to share intelligence and support strategic activities.Supporting the design and execution of competitive planning ... global pharmaceutical and biotech industries, with in-depth knowledge of drug discovery and development processes.Superior stakeholder management skills and ability… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …Management Summer Intern for 2026 (full-time, ~37.5 hours/week) to support the R&D Operations Transformation Enablement Office.Responsibilities: The intern will ... by leveraging people, data, science, and technology to enhance the drug development process.Based on individual skills and background, internship activities may… more
- Eisai, Inc (Fort Worth, TX)
- …strategic thinking, and special projects ESSENTIAL FUNCTIONS:\\ Product/Therapeutic Area Support to Stakeholders Act as the primary clinical/scientific resource to ... scientific data on Eisai's products and relevant therapeutic areas, as requested. Support assigned professional congresses in accordance with MSL plan. Be prepared… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …strategies with the FDA to providing medical education and collecting data to support efficacy and new product development, CMR is involved. The one thing that ... external stakeholders to ensure consistent, accurate communication of medical and drug information and Leads cross-functional and/or global initiatives in response… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …position will be responsible for providing operational excellence continuous improvement support to the cGMP Clinical and Commercial Cell Therapy Manufacturing ... will lead continuous improvement initiatives with various site functions to support of personalized cell therapy production through safe and compliant manufacturing… more
- Merck & Co. (North Wales, PA)
- …data standard deliverables for world-wide regulatory application submissions of drug and vaccine clinical development projects.Be accountable for submission data ... company's electronic submission process and providing tools and templates to support delivery focusing on traceability, quality assurance, data conformance-and data… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …issues resulting in the delay of investigation closure and product release. Support regulatory inspections and audits by ensuring inspection readiness within facility ... an SME during the execution of regulatory inspections and audits as needed. Support compliance activities for site Quality Operations in accordance with Legend… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …the quality systems processes within a cell therapy manufacturing facility to support both clinical and commercial requirements in a sterile GMP environment. This ... site.Oversee metrics, trending, and reporting of relevant quality systems records. Support CAPA site governance programDrive continuous improvement of quality systems… more
- Insmed Incorporated (NJ)
- …preferred.Knowledgeable in all aspects of clinical operations, project management, the drug development process, and clinical trial conduct, including systems and ... care you bring to your work each day, with support for how you work, how you grow, and...include:Comprehensive medical, dental, and vision coverage and mental health support , annual wellbeing reimbursement, and access to our Employee… more
