- Legend Biotech USA, Inc. (Raritan, NJ)
- …the promise of an immunotherapy in the treatment of multiple myeloma.Legend Biotech is seeking Document Control Specialist as part of the Quality team based ... in Raritan, NJ.Role OverviewThe QA Document Control Specialist role is an exempt level position with responsibilities for supporting the document … more
- Cipla (Fall River, MA)
- …GMP batch production records as well as SOP's. In this role the Documentation Specialist adheres to the company's document and SOP's procedures while ensuring ... Job Title : Pkg. Documentation Specialist II FLSA Classification : Professional, Exempt Work Location : Fall River, MA Work Hours: General Shift: 8:30AM - 5:00PM… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …understanding of regulatory requirements, policies and guidelinesExperience with Quality Control document reviews and regulatory inspection processesWorking ... 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,… more
- Insmed Incorporated (NJ)
- …You Are:You have a Bachelor's degree along with 2+ years of experience ona document control team using a quality management system, with preference to Veeva.You ... in. Are you?About the Role:We're looking for a Quality Management System (QMS) Specialist on the Analytical Development team to help us expand what's possible for… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …knowledge and expertise in support of GMP investigations, change controls, document control , process improvement, process validation and data management.Partners ... 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… more
- Aequor (Framingham, MA)
- …manufacturing processes to ensure compliance. Conduct review of testing results. Review document and complete inspection of returned goods. May be involved with ... compliance requirements for the methodology transfer from Research to Quality Control . Interpret complex, explicit documentation to ensure quality standards and… more
- TRC Talent Solutions (Clinton, IL)
- Join Our Team as a Production Specialist I in Clinton, IL! Our client is actively seeking a Production Specialist I to join their growing team in Clinton, IL ! ... takes pride in producing high-quality products that make a real impact. As a Production Specialist I , you'll play an essential role in the creation and packaging of… more
- Curtiss-Wright Corporation (Newtown, PA)
- **Quality Systems Document Control Specialist ** The Quality Systems Document Control Specialist is based on-site at our Curtiss-Wright Defense ... processes. Under the direction of the Sr. Quality Manager, the Quality Systems Document Control Specialist is responsible for managing the elements of the… more
- Insight Global (Pleasant Prairie, WI)
- Job Description Our client, a Medical Device Manufacturer, is looking to add a Document Control Specialist to their Pleasant Prairie, WI site. This ... regulated environment. This role is responsible for maintaining the integrity of the document control system, overseeing change control processes, and… more
- Bristol Myers Squibb (Indianapolis, IN)
- …team, RayzeBio aims to be the global leader in radiopharmaceuticals. **Summary** The Document Control Specialist is responsible for the tactical oversight ... control system for a new Radiopharmaceutical facility in Indianapolis, IN. The Document Control Specialist will be a primary contact point for document… more
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