- Legend Biotech USA, Inc. (Raritan, NJ)
- …of an immunotherapy in the treatment of multiple myeloma.Legend Biotech is seeking QC Supervisor as part of the Quality Operations team based in Raritan, NJ. Role ... OverviewThe QC Supervisor is an exempt level position with responsibilities for...the quality control laboratories in support of cell therapy manufacturing . This includes hiring, development and performance management of… more
- AbbVie (Branchburg, NJ)
- …at www.abbvie.com. Follow @abbvie on Twitter, Facebook, Instagram, YouTube and LinkedIn. Onsite position in Branchburg, NJ Job Description Responsible for the daily ... timely completion of production-related cGMP documentation. Responsible for implementing manufacturing procedures. Ensures the effective use of material, equipment,… more
- Bristol Myers Squibb (Summit, NJ)
- …here at BMS with our Cell Therapy team. The **Specialist, Lead Manufacturing Associate, Cell Therapy** manufactures human blood derived components per Standard ... in a controlled, cGMP cleanroom environment under the supervision of Manufacturing Management. Manufacturing Associates adhere to regulatory requirements while… more
- Memorial Sloan-Kettering Cancer Center (New York, NY)
- …and federal accrediting and regulatory organizations regarding blood component manufacturing , patient sample testing, including compliance with OSHA, FDA, NYSDOH, ... Information: + Schedule: 3:00p-11:00p ; on-call approximately every 4 weeks + 100% Onsite + Report to: Manager, Laboratory Medicine - Blood Bank + Location: 327… more
- Bristol Myers Squibb (Summit, NJ)
- …to support product Value Stream outputs according to Current Good Manufacturing Practices (cGMP's) following the current, approved Standard Operating Procedures ... 5+ years relevant work experience required, preferably in a regulated pharmaceutical manufacturing environment + 5+ years' experience in manufacturing , and… more
- Bristol Myers Squibb (Summit, NJ)
- …to support product Value Stream outputs according to Current Good Manufacturing Practices (cGMP's) following the current, approved Standard Operating Procedures ... + 5+ years relevant work experience, preferably in a regulated pharmaceutical manufacturing environment + 5+ years' experience in manufacturing , and supply… more
- Bristol Myers Squibb (Summit, NJ)
- …to support product Value Stream outputs according to Current Good Manufacturing Practices (cGMP's) following the current, approved Standard Operating Procedures ... 7+ years relevant work experience required, preferably in a regulated pharmaceutical manufacturing environment + 7+ years' experience in manufacturing , and… more
- Bristol Myers Squibb (Summit, NJ)
- …to support product Value Stream outputs according to Current Good Manufacturing Practices (cGMP's) following the current, approved Standard Operating Procedures ... 9+ years relevant work experience required, preferably in a regulated pharmaceutical manufacturing environment + 7+ years' experience in manufacturing and supply… more
- Bristol Myers Squibb (Summit, NJ)
- …suite. **Shift Available:** + Wednesday - Saturday (Every other Wednesday off), Onsite Overnight Shift, 5 pm - 5:30 am **Responsibilities:** + Take personal ... years relevant work experience in material management within a manufacturing GMP facility is required. + 2+ years direct... GMP facility is required. + 2+ years direct supervisor / personal management experience. + 1 year experience… more
- Marotta Controls, Inc. (Montville, NJ)
- …Working alongside Sr. Technicians and Engineers, you will engage in onsite training for operating test equipment and contribute to improvement initiatives ... the company. + Maintain all hand tools in clean working condition. + Notify supervisor of any equipment that requires repair. + Identify any routings discrepancy and… more
