- University of Southern California (Los Angeles, CA)
- cGMP Associate Director , Process DevelopmentApply (https://usc.wd5.myworkdayjobs.com/ExternalUSCCareers/job/Los-Angeles-CA Health-Sciences-Campus/ cGMP ... and other biological products for internal/external users. The Associate Director of Process Development ( cGMP ) is responsible for all aspects of… more
- Merck (West Point, PA)
- **Job Description** We are seeking a highly motivated individual for the role of Associate Director , Biologics Down Stream Process Lead within the Enterprise ... Chain. The end-to-end scope includes Drug Substance for all large molecules. The Associate Director is expected to contribute to ongoing business process… more
- Fujifilm (College Station, TX)
- **Position Overview** **_Summary_** **:** The Associate Director (AD) QualityOperationsis responsible for QA oversight of cGMP operations and areas at one of ... TBF, FBF, NCTM or Analytical Development under the guidance of the Sr Director Quality Operations, lead the Quality Operations organization to create a strong… more
- Merck (Durham, NC)
- …the safest and most compliant operation around the network. EMSS has an Associate Director opening for the Vaccine Manufacturing Facility (VMF) maintenance team. ... maintenance efficiency. WORKING RELATIONSHIPS + Reports to Engineering and Maintenance Director + Manages and interacts with employees within own department +… more
- Gilead Sciences, Inc. (Oceanside, CA)
- …Kite Pharma a Gilead Sciences Company has an opportunity for an experienced Associate Director of Downstream Manufacturing Operations at our Oceanside biologics ... the purification and the fill finish and packaging manufacturing teams. The Associate Director of Downstream Manufacturing will be responsible for coordination,… more
- CBRE (San Juan, PR)
- …lab facilities which may include biology, cell/gene therapy, chemistry, pharmaceutical, cGMP process manufacturing, agricultural / food science, vivarium, ... Associate Project Management Director - Life...should be familiar with pharmaceutical current good manufacturing practices ( cGMP ) including commissioning processes. The work will include civil,… more
- Catalent Pharma Solutions (Manassas, VA)
- ** Associate Director , Quality** **Job Summary** Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission is to ... as a member of the Site Leadership Team the ** Associate Director , Quality** is accountable for the...the direct management and guidance in the Quality and cGMP aspects of the organization. The individual will act… more
- United Therapeutics (Silver Spring, MD)
- …therapies that make a difference, we'd love to connect with you about our ** Associate Director , Process Development** role. **For this role you will ... **Who you are** United Therapeutics is seeking a hands-on leader to oversee process development support for a commercially approved monoclonal antibody used in the… more
- Fujifilm (Holly Springs, NC)
- **Position Overview** The Associate Director of Commissioning, Qualification, and Validation (CQV) is responsible for leading and executing CQV activities for a ... to mitigate risks associated with the therapeutic product lifecycle. The Associate Director ,CQVcollaborates with cross-functional teams to drive continuous… more
- Fujifilm (Thousand Oaks, CA)
- **Position Overview** The Associate Director of Program Management will be accountable for the planning and delivery of programs from the point of contract ... process development and early-stage clinical supply through program closure. The Associate Director ensures the organization executes programs in alignment… more