- Merck & Co. (North Wales, PA)
- …, GLOBAL REGULATORY CMC Biologics (R5)Under general supervision of an Executive Director / Senior Director , the Principal Scientist / Director is ... the probability of regulatory success together with risk mitigation measures.Lead the development , communication, and review of the CMC Regulatory Strategy… more
- Merck & Co. (North Wales, PA)
- Job DescriptionThe drug development Project Manager is part of Global Project and Alliance Management (GPAM) which sits in the Research & Division organization of ... our company.- Position Description/Summary: The GPAM Associate Director , Project Manager, is a core member of Early...Project Manager, is a core member of Early Drug Development and/or Late Drug Development Teams, partnering… more
- Tris Pharma (Monmouth Junction, NJ)
- …a pharmaceutical company, with some combination across technical (eg, research, product development , clinical development , regulatory, CMC ) and business (eg, ... privately-owned biopharmaceutical company in the US with a focus on development and commercialization of innovative medicines that address unmet patient needs.… more
- Lilly (Philadelphia, PA)
- …standards, and cost targets. + Collaborate with cross-functional team leaders, including development , CMC regulatory, manufacturing, and supply chain teams, to ... development and manufacturing and incorporate them into the CMC strategy. + Mentor and develop team members, providing...budget, and resource allocation, and provide regular updates to senior management. + Lead other tasks / projects as… more
- Merck (North Wales, PA)
- …GLOBAL REGULATORY CMC Biologics (R5)** Under general supervision of an Executive Director / Senior Director , the Principal Scientist / Director is ... internal regulatory strategies and provides mentoring and coaching to Sr . Scientist and Assoc Principal scientist in support of...success together with risk mitigation measures. + Lead the development , communication, and review of the CMC … more
- Lilly (Philadelphia, PA)
- …requirements applicable to CMC regulatory in applicable geographies + Support CMC development projects as needed from CMC regulatory perspective ... for people around the world. **Position Overview:** The Associate Director - CMC Regulatory is responsible for...maintain tools to effectively communicate the status of ongoing CMC regulatory projects to cross-functional teams and senior… more
- Integra LifeSciences (Plainsboro, NJ)
- …regulatory agencies. **SUPERVISION RECEIVED** Receives minimal supervision from the Director , CMC Quality Operations. **SUPERVISION EXERCISED** Manages personnel ... challenging what's possible and making headway to help improve outcomes. This ** Senior Manager, Quality Operations** will manage and provide oversight on Quality… more
- Merck (West Point, PA)
- …Our Company is seeking a highly motivated candidate for the position of Director , Vaccine Drug Product Development . Vaccine Drug Product Development ... key stakeholders across the organizations such as Quality, Regulatory CMC , and technical functions, to ensure development ...mindset and collaboration with various partners and stakeholders in development The Director will report to the… more
- Merck (North Wales, PA)
- **Job Description** The drug development Project Manager is part of Global Project and Alliance Management (GPAM) which sits in the Research & Division organization ... of our company. **Position Description/Summary:** The GPAM Associate Director , Project Manager, is a core member of Early...Project Manager, is a core member of Early Drug Development and/or Late Drug Development Teams, partnering… more
- Taiho Oncology (Princeton, NJ)
- …across different spend categories, procurement operations and external supplier development and management. Position Summary: Associate Director , Outsourcing ... Associate Director , Outsourcing & Vendor Management Pleasanton, CA, USA...evolving needs of patients. Advanced technology, a world-class clinical development organization, and state-of-the-art facilities: these and other resources… more
- Integra LifeSciences (Plainsboro, NJ)
- …are challenging what's possible and making headway to help improve outcomes. The Director , Manufacturing is a key member of the plant leadership team responsible for ... leading the overall manufacturing operations for Integra's Collagen Manufacturing Center ( CMC ), working within FDA medical device regulations and ISO Standards.… more
- Amicus Therapeutics (Princeton, NJ)
- Executive Director , Program Management Location Princeton, NJ Requisition ID 2277 # of openings 1 Apply Now ... (https://phh.tbe.taleo.net/phh04/ats/careers/v2/applyRequisition?org=AMICUS&cws=37&rid=1323) Executive Director , Program Management Amicus Therapeutics is a global, patient-dedicated… more
- CSL Behring (King Of Prussia, PA)
- …drug development projects.** **Strong knowledge in drug research, development and manufacturing processes of pharmaceuticals ( CMC , non-clinical, clinical, ... often rare conditions. Could you be our next Associate Director , R&D Project Planning Capability Lead? This position is...management practices to support the delivery of our drug development pipeline. You will lead initiatives to develop and… more
