• Merck & Co. (Philadelphia, PA)
    Job DescriptionSupplier Development & Performance Management (SD&PM) collaborates internationally with both internal and external stakeholders to ensure efficient ... Leads, Business Stakeholders, and Third Parties in the robust management of our enterprise Third Party Due Diligence program....be vaccinated against COVID-19 in order to access a facility or meet with stakeholders). -Please understand that, as… more
    HireLifeScience (09/05/24)
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  • American Honda Motor Co Inc (Marysville, OH)
    …the impact to overall supply chain.Key AccountabilitiesMaintain accuracy of systems required to support production (operation standards, parts, GCCS, GPCS) ... foster engagement.Develop and maintain professional communication networks with other facilities to share best practice, reduce duplicate workload, and collaboration… more
    JobGet (09/15/24)
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  • Merck & Co. (Rahway, NJ)
    …releases are delivered on time, within budget, and with minimal risk.The Release Management Senior Specialist is responsible for the following:Work with various ... across EIT, optimizing deployment efficiency and reducing risks.Collaborate closely with project management teams to ensure that release milestones are met, and the… more
    HireLifeScience (09/11/24)
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  • Legend Biotech USA, Inc. (Raritan, NJ)
    …English (verbal and written) and strong communication skillscGMP manufacturingMaintenance, facilities and utilitiesComputerized maintenance management systems ... limited to: support to manufacturing equipment projects, costimprovementinitiatives, asset management , reliability, and business operations.Support facility project… more
    HireLifeScience (08/29/24)
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  • Merck & Co. (Upper Gwynedd, PA)
    Job DescriptionPosition Description: Clinical Specialist The Clinical Specialist position is a combined position of clinical scientist and study management ... of a clinical scientist, study manager, or program lead, the Clinical Specialist may be responsible for but not limited to:Job ResponsibilitiesMaintain clinical… more
    HireLifeScience (09/17/24)
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  • Merck & Co. (Rahway, NJ)
    …and assists with implementing corrective and preventive action plans.Reviews processes, facilities , procedures and management of change documents to assure ... Job DescriptionPosition Description: Specialist , Environmental, Health, and Safety (EHS) As a...research (labs and pilot plants), clinical manufacturing, office, and facility support functions to develop EHS priorities to achieve… more
    HireLifeScience (09/06/24)
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  • Merck & Co. (Durham, NC)
    …meets all regulatory requirements.- Partnering across our internal manufacturing facilities , external contract manufacturers and suppliers we create an ... and expanding your careerThe main function of the Associate Specialist , Quality Control is to receive and transport starting...or learning events, as guided or approved by Quality management Author, review, and approve SOPs Participate in Kaizen… more
    HireLifeScience (09/07/24)
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  • Merck & Co. (Durham, NC)
    …in quality remediation activities, SAP proficiencyExperience with batch release, and quality systems management ;Your role at our company is integral to helping ... the most trusted supplier of pharmaceuticals and health products worldwide. Our facilities , along with our external contractors, suppliers, and partners, comprise an… more
    HireLifeScience (09/14/24)
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  • Merck & Co. (Rahway, NJ)
    Job DescriptionThe Global Supplier Management Group (GSMG) is an organization that plays a pivotal role in driving efficient sourcing practices for our company ... Research procurement) by developing and maintaining excellence in the processes and systems we use, by driving efficiency through our sourcing and contracting work,… more
    HireLifeScience (09/17/24)
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  • Sunrise Systems Inc (Warren, NJ)
    …knowledge of quality systems including CAPA, change control, and document management systems . Requires minimal direction to complete tasks, authority to make ... Job Title: Specialist , QA Engineering Job ID: 24-03763 Location: Warren...management software (eg Blue Mountain RAM) and quality systems software (eg Veeva). Drives use of best practices… more
    JobGet (09/15/24)
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  • 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...to use on the manufacturing floor.Utilize multiple electronic quality systems , batch records and SAP. Work in a team… more
    HireLifeScience (07/26/24)
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  • Legend Biotech USA, Inc. (Raritan, NJ)
    …GDP/GMP, Part 11/Annex 11, PIC/S, MHRA).Operational experience with electronic quality systems .Experience with Document Management Systems (TruVault/Veeva) ... of multiple myeloma.Legend Biotech is seeking QA Document Control Specialist as part of the Quality team based in...is an exempt position responsible for supporting the document management process within a cell therapy manufacturing facility more
    HireLifeScience (07/26/24)
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  • Legend Biotech USA, Inc. (Raritan, NJ)
    …Technical Operations team based in Raritan, NJ. Role OverviewThe Technical Equipment Specialist will be responsible for ensuring equipment/ systems required to ... of on-going clinical and commercial manufacturing as well as facility expansions and improvements.Key Responsibilities Lead implementation of system/equipment… more
    HireLifeScience (07/26/24)
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  • 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...transfer of QC Lab functions to the Raritan cGMP facility to test products.Review and approval of standard operating… more
    HireLifeScience (07/26/24)
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  • Legend Biotech USA, Inc. (Raritan, NJ)
    …is highly desired.Experience with the start-up of new biopharmaceutical manufacturing facilities is preferred.Experience with Trackwise or equivalent systems is ... in the treatment of multiple myeloma.Legend Biotech is seeking Change Control Specialist as part of the Technical Operations team based in Raritan. Role… more
    HireLifeScience (08/17/24)
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  • 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...floor service tasks (ie, kitting and kit cleaning, inventory management and data entry, sample management and… more
    HireLifeScience (07/30/24)
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  • Sunrise Systems Inc (Devens, MA)
    …deliverables to support disposition of materials and batches within the inventory management systems . Assure materials comply with all CLIENT policies, ... AND SCOPE OF POSITION: The Quality Assurance Incoming Material Disposition Specialist is responsible for supporting the incoming inspection and disposition of… more
    JobGet (09/15/24)
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  • Blanchard Valley Health System (Findlay, OH)
    PURPOSE OF THIS POSITION The Denial Management Specialist is responsible for the timely review and accurate identification and follow-up of all initial denial ... notifications from Blanchard Valley Facility and Professional services as well as the appeal...Specialist when identifying trends relating to denials. The specialist will also work with management to… more
    JobGet (09/15/24)
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  • Software Galaxy Systems, LLC (Danbury, CT)
    …Summary of Duties and Responsibilities: . Responsible for monitoring EHS programs at assigned facilities under the direction of the EHS Management team. . The ... Management team. . Monitors and or supervises hazardous waste management at assigned facilities . . Assists in emergency response support and action planning… more
    JobGet (09/15/24)
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  • Merck & Co. (Rahway, NJ)
    …databases development or programming. Demonstrated technical proficiency in Clinical Data Management Systems (ie, Inform, Inform Architect, Central Designer, ... scripts that facilitate the transfer of electronic data files into the Clinical Data Management System (CDMS). A key aspect of your role will be to collaborate with… more
    HireLifeScience (09/06/24)
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