- Merck & Co. (Rahway, NJ)
- …the principles of project management and clinical customer relationship management . Technical Proficiency: familiarity with supply chain systems and software ... and the operational/executional arms within the business.- - The Program Clinical Supplies Project Manager ( Program CSPM)...(ie Bulk Drug Product). Oversees all bulk drug supply management and ensures proper allocation of drug product as… more
- Merck & Co. (Rahway, NJ)
- …program progress, issues, and mitigation plans to the senior management .Innovative mind-set demonstrated by technical accomplishments, external presentations, ... Mammalian Cell Culture, Mentoring Staff, Negotiation, People Leadership, Pharmaceutical Management , Pharmaceutical Process Development, Process Scale Up, Program … more
- Merck & Co. (Rahway, NJ)
- …individual to work in a fast-paced job that provides a high degree of technical , project, and people management responsibility. - This SSO Facility Lead role ... the SSO Pilot Plant leverages significant depth and breadth of scientific, technical , and operational experience to lead and support facility operations, process… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …together to change lives for the better. The Position The Associate Director , Consumer Social Media Strategy is a high-impact, hands-on leadership role responsible ... role translates the corporate digital vision set by the Senior Director into best-in-class digital experiences, driving audience engagement, building brand trust,… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionWe are seeking a seasoned IT SAP Finance Director to lead the design, delivery and continuous improvement of SAP Finance solutions across our ... division. The ideal candidate combines deep technical SAP expertise with business acumen in commercial and...IT Finance on senior leadership forums; communicate strategy, risks, program status and business impact to executives and board… more
- Merck & Co. (Rahway, NJ)
- …Thisposition is responsible for providing strategic program leadership, technical expertise, and project management in the scale-up, ... Job DescriptionThe Associate Director - Device Tech Transfer is a leadership role...business goals, and quality and regulatory compliance.Essential Duties and Responsibilities: Program Leadership and Technical Project Management… more
- Merck & Co. (Rahway, NJ)
- …ongoing relevant reporting for all cyclical processesRun INSPIRE employee recognition program including supplier management and oversightOversight of Equity ... Job DescriptionThe Associate Director , Compensation and Equity Operations is a highly...Administration globally, including participant experience and supplier management .Support process-related escalations with our global service delivery teams… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …projects.Support the enhancement and Global harmonization of the supplier qualification program , including management of the electronic systems for this ... will also manage a team of people leaders and technical professionals within the QA department based on assigned... Review (QMR).Support management of the Quality Management Review (QMR) program .Support continuous improvement efforts… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …capabilities through strategic vendor partnerships. Relationship This job reports to the Senior Director of the GxP Compliance & Technical Operations. This job ... combines the critical functions of patient safety training, compliance curriculum management , and vendor oversight to ensure adherence to regulatory standards while… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionThe USDA Compliance Subject Matter Expert (SME) - Associate Director , will report to the Animal Health Global Quality Compliance and Technical ... and Policy, Licensing and Evaluation (PEL).Develop and maintain global Quality Management System (QMS) documents pertaining to USDA requirements for facility design,… more
- Genmab (NJ)
- …The Director , HEOL Team Lead is responsible for the management of the HEOL team including:Ensure operational excellence of the HEOL team ... fit? Then we would love to have you join us!The RoleGenmab is currently seeking a Director , HEOL (Health Evidence and Outcomes Liaison) Team Lead to be a part of an… more
- Novo Nordisk Inc. (Boulder, CO)
- …across all departments, such as Quality Assurance/ Control, Chemical Development, Program Management , Regulatory, Analytical Development, Materials Management ... both worlds to develop new medicines for patients. The Position The Associate Director of Drug Product Manufacturing is accountable for all clinical drug product… more
- Merck & Co. (Rahway, NJ)
- …such as manufacturing process development and validation, design control, risk management , material and molding, design validation to create and execute design ... execute, design verification strategies for assigned drug-device combination product program (s) for successful clinical introduction(s) and commercial market(s) approval(s).Define… more
- Merck & Co. (Upper Gwynedd, PA)
- Job DescriptionThe Principal Scientist/ Director , Value & Implementation (V&I) Outcomes Research, position resides in the V&I organization, which includes Global ... with HTA agencies, reimbursement decision makers, and national immunization technical advisory groups.Responsibilities and Primary ActivitiesPartners with Medical Affairs… more
- Insmed Incorporated (NJ)
- …for the future of science, we're in. Are you?About the Role:The Associate Director , Clinical Research Scientist will support and work predominately with the Medical ... and operations, regulatory and quality assurance teams, as well as overall program support ensuring the adherence to all standard operating procedures (SOPs).What… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …Scope of role includes DSE, DSI, DSJ, and may include other regions/ management units as needed to reflect changes to the business model.Responsibilities:Strategic ... employee experience into broader HR and organizational strategiesProgram Design and Management :Partner with Regional EX, Culture, and Listening Leads to:Develop and… more
- Insmed Incorporated (NJ)
- …documents provided by Technical Operations or from CMOs to support development program and life cycle management , and ensure they meet current regulatory ... for the future of science, we're in. Are you?About the Role:The Associate Director , Regulatory Affairs, CMC will be responsible for reviewing the CMC post approval… more
- Insmed Incorporated (San Diego, CA)
- …and for the future of science, we're in. Are you?About the Role:The Associate Director , EDC Programming will lead and oversee EDC programming, and database build for ... the subject matter expert (SME) for Medidata Rave, providing technical guidance and support to the team.Review software upgrades...7+ years of experience in EDC programming, configuration, and management of EDC systems, with at least 5 years… more
- Insmed Incorporated (NJ)
- …and protocols/reports.Collaborate cross-functionally with CMC team, Regulatory, Clinical Operations, and Program Management to drive proactive Quality input into ... and for the future of science, we're in. Are you?About the Role:The Sr. Director CMC QA will lead QA CMC oversight for drug products, biologics, and combination… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …Europe, Canada, United States and Japan and may include other regions/ management units as needed to reflect changes to the business model.Responsibilities:Strategic ... and Human Resource Information System (HRIS) team to define/implement program functionality requirements for global HRISReporting and Improvement:Oversee the… more
