- Legend Biotech USA, Inc. (Raritan, NJ)
- …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...the periodic review process for procedures.Issuance of batch related documentation in support of GMP manufacturing.Reconcile GMP documentation… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …an immunotherapy in the treatment of multiple myeloma.Legend Biotech is seeking a QA Change Control Specialist II as part of the Quality team based in Raritan, ... NJ.Role OverviewThe QA Change Control Specialist II role is an exempt...systems and cGMP requirements.Review change controls, SOPs, and other documentation .Require minimal direction to complete tasks, knows how to… more
- Cipla (Fall River, MA)
- Job Title : Pkg. Documentation Specialist II FLSA Classification : Professional, Exempt Work Location : Fall River, MA Work Hours: General Shift: 8:30AM - 5:00PM ... Overview Invagen Pharmaceuticals is searching for experienced candidates for the position of Documentation Specialist . The Documentation Specialist is… more
- Merck & Co. (Durham, NC)
- …filings including technical reports and risk assessmentsAuthor or approve Change Control documentation for complex process, validation, analytical, equipment, ... last several years; currently Durham employs 1,000+ people.Durham's Technology Transfer Specialist will be an energetic, technical leader with strong interpersonal,… more
- Insmed Incorporated (NJ)
- …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 ... be essential to maintaining the integrity, accuracy, and compliance of all documentation within the Technical Operations department. You will be responsible for… more
- Merck & Co. (Rahway, NJ)
- …to create a frictionless flow of data from source systems to regulatory documentation .- - - Under the guidance of dCMC Regulatory Authoring Leadership, the Senior ... Specialist , Regulatory Authoring Business Analyst,-will optimize regulatory authoring processes...capabilities to ensure effective digital solution integration and adoption. Documentation and Project Management Support: The analyst will create… 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...routine tasks and have conceptual understanding of all Quality Control functions and business areas. May need supervision/support to… 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 ... expertise in support of GMP investigations, change controls, document control , process improvement, process validation and data management.Partners with Operational… 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, NJ. ... setting with Quality, Manufacturing Operations, Facilities & Engineering Quality Control , Operations Technical Support, Supply Chain and Planning.RequirementsA minimum… more
- Resideo (Louisville, KY)
- Reporting to a Technical Support Supervisor, the Technical Support Specialist will act as a critical resource for Control4 customers in the custom electronics ... the smart and connected ecosystem. The Control4 Technical Support Specialist will handle technical inquiries, installation guidance, troubleshooting, configuration… more
