- Catalent (Philadelphia, PA)
- QA Supervisor Position Summary Catalent Pharma Solutions in Philadelphia, PA is hiring a QA Supervisor . The QA Supervisor will p rovide Quality Assurance ... located in the Philadelphia area is Catalent's global Center of Excellence for Clinical Supply Packaging. Catalent offers GMP secondary packaging and clinical … more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …research areas centered around rare diseases and immune disorders.SummarySenior clinical operational leader accountable for operational planning and execution of ... FIH, clin pharm patient studies, and Phases 1-3 clinical trials at the study and program level. Responsible...direction of daily activities in support of goals, the supervisor will conduct a performance evaluation against development goals… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …in the treatment of multiple myeloma. Legend Biotech is seeking QA Investigations Supervisor (2nd shift) as part of the Quality team based in Raritan, NJ. ... Role Overview The QA Investigations Supervisor has the responsibilities for providing quality oversight over...production of a personalized cell therapy to support both clinical and commercial requirements in a sterile GMP environment.… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …in the treatment of multiple myeloma. Legend Biotech is seeking an Operations Supervisor (2nd shift) as part of the Technical Operations team based in Raritan, ... NJ. Role Overview The Operations Supervisor is an exempt level position working within Technical...production of a personalized cell therapy to support both clinical and commercial requirements in a sterile cGMP environment.… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …immunotherapy in the treatment of multiple myeloma. Legend Biotech is seeking a Training Supervisor - Operations as part of the Training team based in Raritan, NJ. ... training activities for the overall plant team members who support cGMP Clinical and Commercial Cell Therapy Manufacturing. This individual will oversee the Training… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …of an immunotherapy in the treatment of multiple myeloma. Legend Biotech is seeking a Supervisor , QC Micro as part of the Quality Control team based in Raritan, NJ. ... Role Overview The QC Microbiology Supervisor , CAR-T Manufacturing is an exempt level position with...the manufacturing facility utilized for cell therapy products for clinical trials and commercial operations in a controlled GMP… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …immunotherapy in the treatment of multiple myeloma. Legend Biotech is seeking a Facility Supervisor as part of the Maintenance & Metrology team based in Raritan, NJ. ... Role Overview The CAR-T Facility Supervisor is an exempt level position working within Technical...cross functional areas in support cell therapy production for clinical and commercial patients. Key Responsibilities Supervises an effective… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …in the treatment of multiple myeloma. Legend Biotech is seeking QC Investigations Supervisor as part of the Quality Control team based in Raritan, NJ. Role ... Overview The QC Investigations Supervisor is an exempt level position with responsibilities for...related to the manufacturing of cell therapy products for clinical trials and commercial operations in a controlled GMP… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …in the treatment of multiple myeloma. Legend Biotech is seeking a Warehouse Supervisor as part of the Technical Operations team based in Raritan. Role Overview ... The Warehouse Supervisor will be part of the Technical Operations team...production of a personalized cell therapy to support both clinical and commercial requirements in a sterile cGMP environment.… more
- Catalent (Manassas, VA)
- …services to solve difficult development and manufacturing challenges.The Quality Assurance Supervisor will lead Food Safety and Quality programs. This includes ... health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …around rare diseases and immune disorders.Summary Assist in planning and execution of clinical studies, under the supervision of the Study Manager role the Study ... Associate Manager within Clinical Operations, in adherence to the protocol, Good ...reports and elevate issues to the attention of the supervisor .Compile and maintain a monitoring review spreadsheet.Compile and maintain… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …rare diseases and immune disorders. Summary Assist in planning and execution of clinical studies, under the supervision of the Study Manager role the Study Associate ... Manager within Clinical Operations, in adherence to the protocol, Good ...reports and elevate issues to the attention of the supervisor .Compile and maintain a monitoring review spreadsheet.Compile and maintain… more
- Catalent (San Diego, CA)
- …Lead discussions with clients on technical topics relating to their project. Supervisor will not need to attend most client meetings.Exercise technical discretion ... design, execution and interpretation of experiments independently with minimal supervisor assistance. Data interpretation should be conducted independently.Assist in… more
- Catalent (Philadelphia, PA)
- …PA is hiring a QA Inspector. This position reports to the Quality Supervisor . The Quality Inspector is responsible for process monitoring and auditing of packaging ... located in the Philadelphia area is Catalent's global Center of Excellence for Clinical Supply Packaging. Catalent offers GMP secondary packaging and clinical … more
- Merck & Co. (Grand Rapids, MI)
- …impact of those options on patients.- Understand the significance and use of clinical trials in multiple tumor types/therapies, both in impact on promoted products ... short- and long-term account plans in collaboration with the account team and supervisor (known as the Oncology Customer Team Leader). Share learnings and best… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …of materials related to manufacturing of autologous CAR-T products for clinical trials and commercial operation in a controlled cGMP environment. Reviews, ... handling tasks in a backup role, as needed. Updates supervisor /manager of work status or problems with recommendations for...of 2 years of experience with quality support in clinical manufacture or NPI is preferred. Experience in … more
- Catalent (St. Petersburg, FL)
- …activities and schedule for the QA Specialists.Provides feedback to QA Supervisor and Manager on performance of QA Specialists.Responsible for actively identifying ... DRB (Deviation Review Board) presentation.Effective communication with Quality Assurance Supervisor and Manager regarding status of daily work.Serve as administrator… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …systems processes within a cell therapy manufacturing facility to support both clinical and commercial requirements in a sterile GMP environment. This role will ... get resources and information from established internal contacts, and consult with supervisor for decisions outside established processes Requirements A minimum of a… more
- Catalent (San Diego, CA)
- …development, GMP manufacturing and stability storage and testing as well as Clinical Supply Services. At Catalent San Diego, we recruit and develop exceptional ... is performed within required timelinesParticipate in technical discussions with supervisor and peers. Communicate with clients and intra-company personnel, including… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …Statistical Analysis Plan (SAP), Statistical Analysis, Results Interpretation, and Clinical Study Report (CSR): Leads statistical activities for very complex ... Research statistical methodologies and addresses specific statistical issues in the design of clinical studies from preclinical through Phase 3 and 4.- CRO / Vendor… more
