- Novo Nordisk Inc. (Boulder, CO)
- …the Boulder facility complies with all applicable environmental, health and safety regulations. Relationships Reports to the Associate Director, EHS. Internal ... valued vendors. Essential Functions Manage the maintenance and implementation of safety programs, compliance plans, and initiatives with primary focus on… more
- Eisai, Inc (Nutley, NJ)
- …we want to hear from you. Job Summary The Oncology Sales Specialist is responsible for meeting/exceeding sales goals through promoting Oncology therapeutic products ... assigned territory in a compliant and appropriate manner. The Oncology Sales Specialist represents and promotes assigned brand(s) in the oral markets with approved… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …in the treatment of multiple myeloma.Legend Biotech is seeking Change Control Specialist as part of the Technical Operations team based in Raritan. Role ... OverviewThe Change Control Specialist will be part of the Technical Operations team...maintain timelines.Perform tasks in a manner consistent with the safety policies, quality systems and cGMP requirements.Drive change controls… 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...and work instructions and comply with cGMP regulations and safety guidelines.RequirementsA minimum of 2 years of experience within… more
- Merck & Co. (Durham, NC)
- Job DescriptionGENERAL INFORMATIONWe have an exciting opportunity for a Validation Specialist to join the technical operations team for a capital project start-up in ... filling, lyophilization, product inspection, and quality control laboratories. The Validation Specialist is responsible for providing technical support to one of the… more
- Merck & Co. (Durham, NC)
- …the bulk active ingredient, finished product, and laboratory testing for vaccine.The Specialist , Quality Control participates in a team of analysts in the ... equipment validation, and GMP laboratory readiness.- The Quality Operations Laboratory Specialist performs laboratory testing on a variety of product samples,… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …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...compliance. Perform tasks in a manner consistent with the safety policies, quality systems and cGMP requirements. Other duties… more
- Merck & Co. (Durham, NC)
- Job Description Position Description: Associate Specialist , Quality Responsibilities:Conducts testing and associated tasks without errors per applicable SOPs and ... procedures in order to maintain compliance with legal regulations, health and safety , and regulatory requirements as writtenWorks in a team environment to accomplish… more
- Merck & Co. (Durham, NC)
- …be responsible for aligning maintenance projects with the business objectives around Safety , Compliance and Cost.- The Senior Mechanical Services Engineer must be ... and maintenance activities are completed in accordance with established safety , GMP, and calibration/maintenance proceduresWork with the Operations, Technology,… more
- Merck & Co. (Durham, NC)
- Job DescriptionThe Senior Specialist , Quality Control will be responsible for activities that support cGMP and regulatory compliance during microbiological method ... proceduresProvide active support during audits and inspections (regulatory, internal, safety )Assist regulatory groups by providing documentation to support the… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …in the treatment of multiple myeloma.Legend Biotech is seeking an 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 Operations team...format.Perform tasks on time in a manner consistent with safety policies, quality systems, and cGMP requirements.Build strong partnerships… 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...and audits as needed.Consistently perform tasks in adherence with safety policies, quality systems, and cGMP requirements, as well… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …in the treatment of multiple myeloma.Legend Biotech is seeking a QC Microbiology Specialist , Lentivirus CAR-T Manufacturing as part of the Quality team based in ... The current openings are on the third shift.Role OverviewThe QC Microbiology Specialist , Lentivirus Vector (LVV) CAR-T Manufacturing is an exempt level position with… more
- Legend Biotech USA, Inc. (Baltimore, MD)
- …the treatment of multiple myeloma.Legend Biotech is seeking a Sr. Cell Therapy Account Specialist - Washington, DC as part of the Commercial team that will be based ... Remotely. Role OverviewThe Sr. Cell Therapy Account Specialist is responsible for representing Legend's products and services to a defined customer base, generating… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …an immunotherapy in the treatment of multiple myeloma.Legend Biotech is seeking QC Investigations Specialist (1st and 2nd Shift) as part of the Quality team based in ... Raritan, NJ. Role OverviewThe QC Investigations Specialist , CAR-T Manufacturing is an exempt level position with responsibilities for leading deviations and… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …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...driving compliance.Perform tasks in a manner consistent with the safety policies, quality systems and cGMP requirements.Critically support investigations… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …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 cell therapy… more
- Novo Nordisk Inc. (Durham, NC)
- …& support validation concepts & approaches for audits & inspections Follow all safety & environmental requirements in the performance of duties Operate in alignment ... with NNWay, demonstrating a Quality & cLEAN® Mindset Provide oversight & administration for the training program Other accountabilities, as assigned Physical Requirements Ability to work in an open office environment with the possibility of frequent… more
- Novo Nordisk Inc. (Durham, NC)
- …ADP, PAS-X & SAP Implements process improvements Observes & enforces all safety & environmental requirements Manages development planning & training process for ... operators on shift Assists with coordination of maintenance tasks on the line Handles simple deviations & assists with unplanned production issues Assists with Sample coordination Other accountabilities, as assigned Physical Requirements Moves equipment &/or… more
- Sysco (Rockford, IL)
- …level of safety awareness.Hire review, coach, and develop the position of safety specialist . Monitoring work, adherence to policy and safety requirement. ... be on-site and travel between facilities with an alternating schedule.The Safety Manager is responsible for leading the implementation of prevention-focused… more
