- Otsuka America Pharmaceutical Inc. (Princeton, NJ)
- **Job Description** The Associate Director of Commercial Strategic Sourcing will lead and manage all aspects of the commercial strategic sourcing and procurement ... services operations. The Associate Director of Commercial Strategic Sourcing has overall ownership...+ Ensures appropriate controls are in place to meet regulatory requirements (ie J-sox, Third Party Risk Management, etc.)… more
- Veterans Affairs, Veterans Health Administration (Cleveland, OH)
- Summary The VA Northeast Ohio Healthcare System is recruiting for a Associate Chief of Imaging Diagnostic Radiology. The Associate Chief of Imaging Diagnostic ... Radiology will function in Imaging Service. Responsibilities The Associate Chief of the Imaging Service is one of...position are subject to urinalysis to screen for illegal drug use prior to appointment. Applicants who refuse to… more
- Rhythm Pharmaceuticals (Boston, MA)
- …adapt, learn, and our tenacity to overcome barriers, together. Opportunity Overview The Sr. Associate , Analytical Chemistry will be a member of the Tech Ops team and ... of testing performed at Rhythm's contract sites for the manufacturing and testing of Drug Substance and Drug Product. This position will s upport analytical… more
- Lilly (Indianapolis, IN)
- …within Bioproduct Research and Development (BRD) is responsible for the manufacture of drug substance (DS) to support clinical trials within the BRD portfolio. This ... as oversight of DS manufacturing at qualified collaboration partners. The Associate Director for Technical Services manages functional responsibilities for the… more
- BioBridge Global (San Antonio, TX)
- …and Risk Functions will be performed with support from Global Quality and Regulatory leadership. Commit to and abide by the character of BioBridge Global's Core ... and respond to applicable environmental safety Federal, State or Local regulatory inquiries, concerns and inspections. Collaborate on the investigation of workplace… more
- Regeneron Pharmaceuticals (Armonk, NY)
- The Manager, Clinical Drug Supply & Logistics is responsible for forecasting Investigational Product (IP) supply requirements for multiple clinical trials and for ... within budget and with good quality, in compliance with Regulatory Authorities' regulations / guidelines and Regeneron SOPs /...stability). **A Typical Day Includes:** + Serves as lead drug supply manager of multiple small and/or less complex… more
- Gilead Sciences, Inc. (Foster City, CA)
- …The successful candidate will contribute to the development of formulation and drug product processes for innovative molecules to support toxicology and early ... successfully execute experiments and activities to support formulation and drug process development, including molecular assessment, First-in-Human formulation development,… more
- Gilead Sciences, Inc. (Foster City, CA)
- …and CAPA management team within Gilead R&D Quality on internal audits, regulatory agency inspections, risk assessment, deviations and CAPA activities + Liaison and ... including authoring and reviewing SOPs, facilitating internal audits, supporting regulatory inspections, developing and managing CAPAs and deviations, and training… more
- The Boeing Company (El Segundo, CA)
- …The Boeing Company is looking for a **Thermal Development Lab (TDL) Operations Engineer ( Associate , Mid-Level or Senior)** to join our team in **El Segundo, CA** . ... and maintains documentation that supports both internal and external regulatory requirements including EHS + Develops operating and maintenance...the immediate area or relocate at their own expense. ** Drug Free Workplace:** Boeing is a Drug … more
- Sanford Health (Sioux Falls, SD)
- …**Weekly Hours:** 40.00 **Salary Range:** 17.50 - 28.00 **Job Summary** The Associate Credentialing Specialist is responsible for tasks and processes developed to ... and external customer communications. Responsible for planning work to meet regulatory and customer defined deadlines, which requires coordination to minimize… more