- Legend Biotech USA, Inc. (Raritan, NJ)
- …treatment of multiple myeloma. Legend Biotech is seeking a Master Data Governance Sr. Specialist as part of the Technical Operations team based in Raritan, NJ. Role ... Overview We are actively seeking a proficient SAP Master Data Sr. Specialist with a specific focus on Materials orchestration throughout the End-to-End Manufacturing… more
- Merck & Co. (Durham, NC)
- Job Description P1 : Process Support Lab Associate Specialist Job Description: The Maurice R. Hilleman Center for Vaccine Manufacturing is located in Durham, NC. ... vaccine tech transfers to the facility.The Process Support Lab Associate Specialist will be an energetic, technical contributor with strong interpersonal,… more
- Aequor (Devers, TX)
- …the needs of the business warrant.JOB SUMMARY is seeking a Contractor Field QA Specialist for the QA Operations organization at the LSCC in Devens, MA. The ... Contractor Field QA Specialist is responsible for quality activities for the LSCC...review of manufacturing batch records. Review manufacturing shop floor documentation . EDUCATION REQUIREMENTS High School Degree required Relevant college… more
- Merck & Co. (Rahway, NJ)
- …a high degree of technical and project management responsibility. The Senior Specialist - Manufacturing Automation position will report to the Director, Engineering, ... utility systems and associated infrastructure.- Responsibilities of the Senior Specialist - Manufacturing Automation include the following:The automation engineer… more
- Merck & Co. (Rahway, NJ)
- …a high degree of technical and project management responsibility. The Specialist -Engineering position will report to the Associate Director, Engineering and ... scaling up new chemistries, and exploring new technologies. - Responsibilities of the Specialist - Engineer include the following: The engineer role at the … more
- BioAgilytix (Durham, NC)
- …Quality Control (QC) technical, scientific, and compliance review of data and documentation generated by the Bioanalytical Operations group in support of regulated ... studies (eg GLP, GMP).Identify deviations, OOS and OOT associated with Bioanalytical Operations data as applicableIssue QC review observations and work closely with the scientific staff to ensure data integrityCollect metrics data used to monitor the QC… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …in the treatment of multiple myeloma. Legend Biotech is seeking a CQV Specialist (Contract Position) as part of the Technical Operations team based in Raritan, ... creation, revision and review of change controls, SOPs, and other documentation Participates in authoring Risk Assessments, FMEAs, Periodic Qualifications, Project… more
- Aequor (TX)
- …the maintenance of Product and QS EC Certificates (MDD /MDR) and associated documentation . Assist with the coordination and scheduling of NB meetings for Alcon SMEs ... as required, including documenting and filing of NB meeting minutes. Support NBL team and Alcon QMS in coordination and execution of NB audits. Collaborate with the MDR PMs, GRA strategists and cross- functional teams to support MDR Sub. Strategy and… more
- Novo Nordisk Inc. (West Lebanon, IN)
- …is responsible for performing reviews of manufacturing and support documentation and records to certify compliance with in-house specifications/standards and ... assess Corrective and Preventive Actions Reviews and approves validation documentation Reviews and assesses deviations; includes tracking, follow-up and… more
- Shimadzu Scientific Instruments (Los Angeles, CA)
- …technical training to customers, service, and technical support personnel. (daily) Accurate documentation and reporting of all repairs and product failures and when ... with necessary telephone technical support, repair parts shipments and documentation required to effect instrument repairs, maintenance, and installations. (daily)… more
- Merck & Co. (North Wales, PA)
- …proof of concepts using Jupyter Notebooks and create technical documentation as needed.Requirements:Bachelor's degree or equivalent in Mathematics, Computer Science, ... Engineering, Artificial Intelligence, or a related field and 5 years of experience in the position offered or related.Must have 5 years of experience with all of the following: SQL and PySpark; Git, Docker, and Terraform; Agile Methodology; and experience with… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …of an immunotherapy in the treatment of multiple myeloma. Legend Biotech is seeking QC Specialist , Lab Services - I, II, III as part of the Quality team based in ... Raritan, NJ. Role Overview The QC Specialist , Lab Services, is responsible for sample management. The QC Specialist is encouraged to work independently on… more
- Novo Nordisk Inc. (West Lebanon, IN)
- …(generate, execute, and evaluate change requests) Revise and create documentation (SOP, batch records, reports) associated with technical operations, production, ... engineering, and validation Incorporate technical pre-planned process improvements and cost reduction projects into manufacturing Develop training for engineering/validation or production with direction from engineers Support Health Authority inspections and… more
- Novo Nordisk Inc. (West Lebanon, IN)
- …is responsible for performing reviews of manufacturing and support documentation and records to certify compliance with in-house specifications/standards and ... signature authority for deviation closure Reviews and approves Validation Documentation Reviews and assesses Corrective and Preventive Action Reports Participates… more
- Novo Nordisk Inc. (West Lebanon, IN)
- …to support manufacturing operations. Focus areas may include Training, Documentation , Deviations, Change Control and Projects. Drives the coordination and ... process/equipment improvements and data trending/analysis Review/approval of completed process documentation Ability to train others on the manufacturing equipment… 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 Overview The ... QA Warehouse Incoming/Raw Material Specialist is an exempt level position with responsibility to...and record results to complete receipt process. Reviews inspection documentation (C of A or other Material Certifications) for… more
- Atrium Health (Charlotte, NC)
- …with system strategy, vision, mission, and goals. Ensures competency of Clinical Documentation Specialist staff by conducting on-going reviews and skills ... Overview Job Summary The Advocate Health Condition Management and Documentation team is excited to announce an opening for...will be a key subject matter expert for clinical documentation and risk adjustment coding within the enterprise. This… more
- Merck & Co. (Rahway, NJ)
- …solutions for tomorrow. The position of ServiceNow CMDB & Discovery Specialist has responsibility for s upporting the standardization, design, implementation, and ... (ie, ServiceNow API, ServiceNow Service Graph Connector)ServiceNow Certified Implementation Specialist , Certified System Administrator (CSA), or Certified Application Developer… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …of Product patient Safety's case processing activities, which include the receipt, documentation , triage, case review, and quality assessment of all inbound safety ... requirements, and supplier relations In collaboration with Patient Safety training specialist and people managers, support internal and external training activities… more
- Merck & Co. (Rahway, NJ)
- …for tomorrow. The position of CMDB & Discovery Analyst / Sr. Specialist has responsibility for s upporting the standardization, design, implementation, governance, ... leading practice identification, solution design, taxonomy modelling, construction, implementation, documentation , and performance metrics.Presenting and articulating process improvement and… more
