- Merck & Co. (Durham, NC)
- …while developing and expanding your careerThe main function of the Associate Specialist , Quality Control is to receive and transport starting materials ... adds value to the achievement of team goals Functional Expertise The Associate Specialist , Quality Control - will be responsible for performing Sample Transfers,… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …to maintain timelines.Perform tasks in a manner consistent with the safety policies, quality systems and cGMP requirements.Drive change controls to ensure on ... in the treatment of multiple myeloma.Legend Biotech is seeking Change Control Specialist as part of the Technical Operations team based in Raritan. Role… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …an immunotherapy in the treatment of multiple myeloma.Legend Biotech is seeking Warehouse Specialist as part of the Technical Operations team based in Raritan. Role ... OverviewThe Warehouse Specialist will be part of the Technical Operations team...support both clinical and commercial requirements in a sterile cGMP environment. The individual will work closely and collaboratively… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …in the treatment of multiple myeloma.Legend Biotech is seeking Operations Inventory Control Specialist as part of the Technical Operations team based in Raritan, New ... Jersey. Role OverviewThe Operations Inventory Control Specialist will be part of the Raritan CAR-T Operations...start of a personalized clinical cell therapy site meeting cGMP requirements. This individual will serve as the point… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …an immunotherapy in the treatment of multiple myeloma.Legend Biotech is seeking Maintenance Specialist as part of the Technical Operations team based in Raritan, New ... will be responsible for maintenance support and mechanical system operations for cGMP Clinical and Commercial Cell Therapy Manufacturing on a modified second shift.… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …immunotherapy in the treatment of multiple myeloma.Legend Biotech is seeking QA Lab Oversight Specialist as part of the Quality team based in Raritan. Role ... OverviewThe QA Lab Oversight Specialist role is an exempt level position with responsibilities...tasks in a manner consistent with the safety policies, quality systems and cGMP requirements.Critically support investigations… more
- Merck & Co. (Rahway, NJ)
- …located in Rahway, New Jersey includes a state-of-the-art sterile drug product cGMP clinical supply manufacturing facility known as FLEx Sterile that is currently ... vaccines, antibody drug conjugates (ADCs), in addition to others.- --The Senior Specialist , Engineering will serve as a business representative in the FLEx Sterile… more
- Aequor (Providence, RI)
- …investigations. The Specialist Stability builds and monitors stability studies within quality systems (eg LIMS), owns and handles product quality and ... vital role, you will provide support to the Product Quality (PQ) organization as a subject matter expert of...drug product manufacturing and analytical techniques General knowledge of cGMP and US and international filing regulations pertaining to… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …a QC Microbiology Specialist , Lentivirus CAR-T Manufacturing as part of the Quality team based in Raritan, NJ. The current openings are on the third shift.Role ... OverviewThe QC Microbiology Specialist , Lentivirus Vector (LVV) CAR-T Manufacturing is an exempt...tasks in a manner consistent with the safety policies, quality systems and cGMP requirementsOther duties will… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …in the treatment of multiple myeloma.Legend Biotech is seeking a QA Shop Floor Specialist as part of the Quality Operations team based in Raritan, New ... Jersey. Role OverviewThe QA Shop Floor Specialist is an exempt level position responsible for the...cGMP cleanroom environment. This position is responsible for quality and maintaining the highest standards in compliance within… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …treatment of multiple myeloma.Legend Biotech is seeking a QA Warehouse Incoming Raw Material Specialist as part of the Quality team based in Raritan, NJ. Role ... OverviewThe QA Warehouse Incoming/Raw Material Specialist is an exempt level position with responsibility to...tasks in a manner consistent with the safety policies, quality systems and cGMP requirements. Other duties… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …format.Perform tasks on time in a manner consistent with safety policies, quality systems, and cGMP requirements.Build strong partnerships with Manufacturing, ... of multiple myeloma.Legend Biotech is seeking an Operations Support Specialist as part of the Technical Operations team based...support both clinical and commercial requirements in a sterile cGMP environment. Job duties will be performed within a… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …in the treatment of multiple myeloma.Legend Biotech is seeking an Operations Specialist as part of the Technical Operations team based in Raritan, NJ.Role ... position will be responsible for providing operational support to the cGMP Clinical and Commercial Cell Therapy Manufacturing plant. This individual will… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …immunotherapy in the treatment of multiple myeloma.Legend Biotech is seeking QA Document Control Specialist as part of the Quality team based in Raritan, NJ. ... Role OverviewThe Quality Assurance Document Control Specialist role is an exempt position responsible for supporting the document management process within a… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …actions (CAPA).Perform tasks in a manner consistent with the safety policies, quality systems and cGMP requirements.RequirementsMinimum of a Bachelor's Degree in ... treatment of multiple myeloma.Legend Biotech is seeking QC Investigations Specialist (1st and 2nd Shift) as part of the... (1st and 2nd Shift) as part of the Quality team based in Raritan, NJ. Role OverviewThe QC… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …promise of an immunotherapy in the treatment of multiple myeloma.Legend Biotech is seeking QC Specialist , Lab Services - I, II, III as part of the Quality team ... based in Raritan, NJ. Role OverviewThe QC Specialist , Lab Services, is responsible for sample management. The...on routine tasks and have conceptual understanding of all Quality Control functions and business areas. May need supervision/support… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …bioassay, cell biology and immunology experience. This individual will be providing specialist knowledge and expertise of cell and gene therapy analytical methods, ... that integrates with eLIMS and MES to manage samples from manufacturing in cGMP through final testing results. The scope comprises of defining changes to current… more
- Careers Integrated Resources Inc (Frederick, MD)
- Job Title: Cell Therapy Specialist Location: Frederick, MD Duration: 12 Months (Possible extension) Pay range: $32 /hour on W2. For the first 7 weeks of the ... . We are seeking a highly motivated, Cell Therapy Specialist to join our newly formed Cell Therapy Manufacturing...execute GMP runs in close collaboration with Materials Management, Quality Control and Quality Assurance. . Are… more
- Sunrise Systems Inc (Fort Worth, TX)
- Job Title: Quality Specialist -Jr Location: Fort Worth, TX Duration: 03 months on W2 Contract with Extension possible. Role Overview: The Quality ... author non-conformances to decrease the site backlog. Competences: Knowledge of cGMP , ICH, FDA guidance and regulations Strong computer, scientific, and… more
- Sunrise Systems Inc (Devens, MA)
- …performing review or verification work PURPOSE AND SCOPE OF POSITION: The Quality Assurance Incoming Material Disposition Specialist is responsible for ... Knowledge, Skills, and Abilities Experience in a laboratory, manufacturing, quality , or warehouse environment desired. Prior evidence of successful participation… more
