- Otsuka America Pharmaceutical Inc. (Trenton, NJ)
- **Job Summary** The Associate Director , Global Product Quality - Biologics is responsible for directing quality oversight of clinical and commercial ... as well as drive continuous improvement. **Job Description** + Responsible for directing quality oversight of GMP contract manufacturers of Otsuka clinical and… more
- Bristol Myers Squibb (Madison, NJ)
- …more: careers.bms.com/working-with-us . **Position Summary** Bristol-Myers Squibb is seeking an Associate Director , Principal Product Quality Leader (PQL), ... and cell therapy projects) to ensure regulatory compliance of GMP operations in support of the program.The PQL must...should be directed to Chat with Ripley. R1597688 : Associate Director , Principal Product Quality … more
- Otsuka America Pharmaceutical Inc. (Trenton, NJ)
- **Job Summary** The Associate Director Controlled Substances, Quality Global Product Quality - API/DP is responsible for directing quality oversight ... well as drive continuous improvement. **Job Description** + Responsible for directing quality oversight of GMP contract manufacturers of controlled substances… more
- Otsuka America Pharmaceutical Inc. (Trenton, NJ)
- The Associate Director of Global Supplier Quality will be responsible for the execution of supplier quality audit and monitoring across the company's ... , with 2+ years in supplier or external manufacturing quality . + Strong knowledge of GMP regulations...external manufacturing quality . + Strong knowledge of GMP regulations for small molecules and/or biologics. + Experience… more
- Merck (Rahway, NJ)
- …of eight years of experience in engineering, logistics, planning, procurement, quality , or related disciplines. + Strong interpersonal and leadership skills, ... Combination Products, Cross-Functional Teamwork, Deviation Management, Good Manufacturing Practices ( GMP ), Leadership, Manufacturing Scale-Up, New Product Introduction Process, Packaging… more
- Parexel (Trenton, NJ)
- …associated with audits and regulatory inspections in liaison with LSAD and Clinical Quality Associate Director (CQAD). + Ensures timely collection/uploading ... other CRAs and the Local Study Team/ Local Study Associate Director (LSAD) to ensure that study...site staff in study related matters, including Risk Based Quality Management (RbQM) principles. + Confirms that site staff… more
- Parexel (Trenton, NJ)
- …associated with audits and regulatory inspections in liaison with LSAD and Clinical Quality Associate Director (CQAD). + Ensures timely collection/uploading ... other CRAs and the Local Study Team/ Local Study Associate Director (LSAD) to ensure that study...site staff in study related matters, including Risk Based Quality Management (RbQM) principles. + Confirms that site staff… more
- Atlantic Health System (NJ)
- …the Production Manager in the overall management of operations to include quality , product safety, associate safety, making production metrics, staffing, ... Safety Inspection Service issues and compliance with Good Manufacturing Practices ( GMP ), USDA requirements and State Agricultural standards. 2. Ensures performance… more
- BD (Becton, Dickinson and Company) (Franklin Lakes, NJ)
- …part of the Materials Science team in Franklin Lakes NJ, reporting to the Associate Director , Materials Science. Our R&D Engineers and Scientists are responsible ... compliance with all local, state, federal and BD safety regulations, quality policies, best practices, and procedures through appropriate communication. The Staff… more
- BeOne Medicines (Pennington, NJ)
- …and authoring of various reports. This position reports directly into the Associate Director , Manufacturing Science and Technology (MST) Cell Culture and ... position involves close collaboration with Manufacturing, Supply Chain, Procurement, Quality Control, Quality Assurance, Regulatory, Process Development groups… more