- Merck & Co. (Rahway, NJ)
- …a high degree of technical and project management responsibility. The Specialist - Process/Facility Engineering position will report to the Director, Engineering ... production, utility systems and associated infrastructure.- Responsibilities of the Specialist - Process/Facility Engineer include the following:The process engineer… more
- Lovelace Biomedical Research Institute (Albuquerque, NM)
- OverviewUnder specific direction, the Accounts Payable Specialist will be responsible for timely and accurate processing of accounts payable disbursements and ... for payments, process 1099s, file and organize processed vouchers and associated documentation , reconcile credit card/expense reports, perform data entry of a wide… more
- Novo Nordisk Inc. (Boulder, CO)
- …are driving change. Are you ready to make a difference? The Position The Specialist , API Manufacturing works in Novo Nordisk's Boulder, Colorado Pilot Plant and is ... ensuring the supply of API and meeting production goals, the Specialist , API Manufacturing actively supports continuous improvement initiatives and identifies… more
- Merck & Co. (Durham, NC)
- Job DescriptionPosition Description: Senior Specialist , Manufacturing Automation The Senior Specialist Manufacturing Automation person is primarily responsible ... the automation systems in compliance with cGMPs. The Manufacturing Automation Sr. Specialist must actively support, participate and embrace an empowered team culture… more
- Merck & Co. (Millsboro, DE)
- …on time, every time, across the globe.The Quality Control (QC) Associate Specialist , with Guidance from the QC Manager, ensures product/process quality through the ... review of GMP documentation and performs activities to ensure the efficient testing...release of antigen and seed batches. The QC associate specialist must adhere to regulatory and site policies and… more
- 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)
- …medicines and vaccines, including our HPV vaccines. - The Senior Engineering Specialist will troubleshoot and maintain process and process support equipment utilized ... and Preventative Maintenance (PM's) plans, as requested. Responsible for written documentation of activities. Responsible for SAP transactions and change control… 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)
- …job that provides both technical and project management responsibility. The Specialist - Manufacturing Automation position will report to the Director, Engineering, ... production, utility systems and associated infrastructure.- Responsibilities of the Specialist - Manufacturing Automation include the following:The automation engineer… more
- Merck & Co. (Durham, NC)
- …review and approval of incursions, review and approval of batch record documentation , and Reports.Requires working high level of knowledge and experience in the ... and environmental monitoring matters.Review and approval of batch record documentation (electronic batch record comment resolution, autoclave records, review and… more
- Novo Nordisk Inc. (Durham, NC)
- …Performs quality review & approval of Change Requests (CR's) & other documentation (in conjunction with LoB). Performs archiving duties and QA presence & ... ISO standards, corporate & local SOPs Reviews & approves documentation for Quality approval - batch records & other... for Quality approval - batch records & other documentation Supports & reviews investigations & root-cause analysis Participates… 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
- 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
- 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
- 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
- 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
- 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
