- Legend Biotech USA, Inc. (Raritan, NJ)
- …immunotherapy in the treatment of multiple myeloma.Legend Biotech is seeking Operations Support Specialist as part of the Technical Operations team based in ... Raritan, NJ. Role OverviewThe Operations Support Specialist will be part of the Technical...within cell therapy Technical Operations.Requirements HS Diploma with relevant experience required; or Certificate or Associate's degree in a… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …in the treatment of multiple myeloma.Legend Biotech is seeking a QA Shop Floor Specialist III 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 floor quality oversight of the production of autologous CAR-T… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …of an immunotherapy in the treatment of multiple myeloma.Legend Biotech is seeking QC Specialist , Lab Services, II/III as part of the Quality team based in ... Raritan, NJ. Role OverviewThe QC Specialist , Lab Services is responsible for sample management. The...degree or higherA minimum of two (2) years related experience in medical device, biopharmaceutical, or pharmaceutical industryA degree… more
- Capital One (Riverwoods, IL)
- Manager, Systems Specialist Operations (Global Payment Network) This is an exciting opportunity to partner with world class professionals to solve real business ... and identify enhancements to give our customers the best experience in the industry. Responsibilities: Strategy development and implementation...pay at the time of this posting. Salaries for part -time roles will be prorated based upon the agreed… more
- Insmed Incorporated (NJ)
- …you'll be part of a community that prioritizes the human experience , celebrates curiosity, and values every person's contributions to meaningful progress. That ... diseases. We are seeking an authentic and experienced Therapeutic Specialist with a proven track record of success in...must possess a high level of clinical aptitude and experience in a portfolio selling environment to effectively engage… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …of an immunotherapy in the treatment of multiple myeloma.Legend Biotech is seeking CQV Specialist II as part of the Technical Operations team based in Raritan, ... to cGMP requirements. This role will require CQV and engineering experience , ability to work independently, drive effective communication, coordination and… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …in the treatment of multiple myeloma.Legend Biotech is seeking QA Document Control Specialist I/II/III as part of the Quality team based in Raritan, ... NJ. Role OverviewThe QA Document Control Specialist role is an exempt level position with responsibilities...and guidances (eg 21 CFR, ICH Q10, EU GDP/GMP, Part 11/Annex 11, PIC/S, MHRA)Operational experience with… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …an immunotherapy in the treatment of multiple myeloma.Legend Biotech is seeking QC Investigations Specialist II as part of the Quality team based in Raritan, NJ. ... Role OverviewThe QC Investigations Specialist is an exempt level position with responsibilities for...discipline is required.A Minimum of 4 years relevant work experience , preferably within a biological and/or pharmaceutical industry is… more
- Merck & Co. (Rahway, NJ)
- …similar to what is described in the Pipeline Advertisement.Expand your skills and experience in audit through a career path in the pharmaceutical industry. Become ... part of a dynamic team that offers a flexible...flexible work environment, leadership development programs, travel opportunities and workplace inclusion.We are a leading pharmaceutical company committed to… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …immunotherapy in the treatment of multiple myeloma.Legend Biotech is seeking QA Batch Disposition Specialist II/III as part of the Quality team based in Raritan, ... required in Life Sciences or EngineeringA Minimum of 0-2+ years Biotech/Pharmaceutical experience or equivalent industry experience Knowledge of cGMP regulations… more
