- Merck (West Point, PA)
- **Job Description** The Global Clinical Supply (GCS) organization is accountable for managing the 'end-to-end' integrated clinical supply chain across ... independently, the Program CSPM designs strategic and operational plans for all clinical supply activities associated with the clinical studies in their… more
- Merck (West Point, PA)
- **Job Description** The Global Clinical Supply (GCS) organization is within our company's Research Laboratories and is accountable for managing the 'end-to-end' ... integrated clinical supply chain across our company's portfolio...design, assessment, and improvement of the end-to-end processes. The Associate Director , GCS Process Steward, is accountable… more
- Lilly (Philadelphia, PA)
- …global health by accelerating the development of new medicines. **Responsibilities:** The Associate Director of Contract Manufacturing is responsible for leading ... of cGMP drug substance manufacturing and quality control + Experience in supply chain management of clinical trial material/commercial products highly desirable… more
- Merck (North Wales, PA)
- …markets around the world, with nearly $2.4B in annual revenue. **Position Overview** The Associate Director , MMRV Franchise Manager is a key new role reporting ... updated growth strategy and sponsorship for critical investments across manufacturing, clinical , and commercial areas that the business will execute and deliver… more
- Merck (North Wales, PA)
- **Job Description** **Position Description** Associate Director , Quality Management System Change Control will work with the Change Control core team team, ... + Management processes and systems + Interact with Batch Disposition personnel, clinical , Integrated Product Data team and Regulatory scientists to drive further… more
- Organon & Co. (Plymouth Meeting, PA)
- …Review Committee. + Providing day-to-day legal advice to the labeling, quality, supply chain, and regulatory organizations in R&D and Manufacturing. + Preparing ... and review of regulatory submissions. + Providing legal advice on issues affecting clinical assets and marketed products. + Providing regulatory legal guidance on a… more
- Merck (West Point, PA)
- …of the workflows needed for discovery, preclinical research and product development for clinical supply . Usage of the solutions span from scientific simulations ... including Grace and Gaussian to data intensive simulations using AI/ML and deep learning. Product Manager will work closely with research stakeholders to understand their needs, define and groom backlog, and enable solutions in an agile fashion. This will lead… more
- WuXi AppTec (Philadelphia, PA)
- …drug development by providing all discovery, CMC development and the entire manufacturing supply chain under one roof. With over 1,000 scientists from 9 R&D and ... platform will support your needs in TIDES drug development from discovery through clinical to commercial. Moreover, our Regulatory Affairs CMC team is experienced in… more
- Organon & Co. (Plymouth Meeting, PA)
- … or Executive Director in Organon Regulatory CMC New Products, the Associate Principal Scientist ( Associate Director ) is responsible for Regulatory ... Chemistry Manufacturing & Controls (CMC) aspects of clinical phase through market product registration for the assigned portfolio of small molecule, biologic,… more
- Penn Medicine (Philadelphia, PA)
- …Nursing, Practice Management, and support staff. Under the leadership of the Associate Director of Radiation Therapy, the Senior Therapy Manager facilitates ... Reviews financial reports independently and as distributed by financial professionals and Director of Radiation Therapy. Actively manages supply and equipment… more