- United Therapeutics (Research Triangle Park, NC)
- …and mentoring or developing a member of your team. The Associate Director , QA Engineering will provide advanced support and subject matter technical expertise ... best practices to maintain cGMP compliance for UTC combination products, clinical materials supply, and new product development of active pharmaceutical ingredients… more
- Bristol Myers Squibb (Devens, MA)
- …place than here at BMS with our Cell Therapy team. The **Associate Director ,** **Process Implementation Lead l** eads the transition of hybrid automated cell therapy ... Devens site. This matrix and direct people manager role drives project milestones, operational readiness, and regulatory compliance, overseeing reports in support… more
- Gilead Sciences, Inc. (Parsippany, NJ)
- …aspirations. Join Gilead and help create possible, together. **Job Description** The ** Director , USMA Strategic Execution** will play a critical role in the ... other functional areas where needed. + Foster stakeholders' understanding of project aims and inherent risks during initial development, shape their expectations… more
- Sanofi Group (Morristown, NJ)
- **Job Title:** GRA Device Lead ( Director ) **Location** : Morristown, NJ, Cambridge, MA, Framingham, MA **About the Job** Are you ready to shape the future of ... The role will represent the GRA Device perspective as a member of project specific cross functional global regulatory team (GRT) and is accountable to develop… more
- BeOne Medicines (Emeryville, CA)
- …+ Lead and/or mentor the program management team for oncology clinical development lifecycle management. + Develop and lead global product development ... job:** + Plan and execute projects in accordance with the global clinical development strategy. + Facilitate alignment with key stakeholders and ensure communication… more
- US Tech Solutions (Holly Springs, NC)
- …preparation, strategy, and execution of Technology Transfer, Process Scale-up, Clinical & Commercial Manufacturing Support, Process Performance Qualification (PPQ) ... examples of Additional Responsibilities: Work cross-functionally with individuals and project teams in Process Development, Manufacturing, Quality, and Facilities… more
- J&J Family of Companies (Spring House, PA)
- …We are searching for the best talent for an **Associate Director , Regulatory Medical Writing** within our Integrated Data Analytics & Reporting ... (eg, manage a subset of TA). + Preparing and finalizing all types of clinical documents, taking a proactive or lead role in terms of content and scientific… more
- Emory Healthcare/Emory University (Atlanta, GA)
- …Program at Emory University is nationally recognized for its excellence in clinical training, academic rigor, and commitment to resident education and well-being. ... With access to a diverse patient population across multiple clinical sites, residents gain comprehensive experience in both inpatient and outpatient settings. The… more
- GE HealthCare (Waukesha, WI)
- **Job Description Summary** The Variable Cost Productivity (VCP) Director plays a pivotal role within the Patient Care Solutions (PCS) Integrated Supply Chain team, ... (eg, teardown labs, should-cost modeling, supplier analytics) while decentralizing clinical , regulatory, and execution decisions to subsegments. + Drive material… more
- Otsuka America Pharmaceutical Inc. (Salem, OR)
- **Associate Director , Small Molecule Analytical Development** + Lead and oversee phase appropriate method development and optimization for drug substance and drug ... release testing and reporting, providing actionable insights and recommendations to optimize project outputs for the project teams and ensure alignment with… more