- Novo Nordisk Inc. (Boulder, CO)
- …With a new laboratory completed in 2021 to support analytical and process development, the CMC team works alongside Quality, Regulatory, Technical Operations and ... 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… 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)
- …GMP clinical manufacturing plant in Rahway, New Jersey.- The role at the Specialist level will be responsible for analyzing monthly forecasts and assessing current ... identify excipients and components that need to be purchased.- The forecasting specialist will ensure that purchased excipients and components are received and… more
- Merck & Co. (Durham, NC)
- …product inspection, and quality control laboratories. The Quality Assurance Specialist will support this expansion. Project activities requiring support include ... the capital project to construct the facility, process and technology introduction, compliance improvements, and manufacturing readiness...floor support in the execution and review of GMP documentation such as IQ, OQ and other technical documents… more
- Merck & Co. (Rahway, NJ)
- Job Description SSO Operations Specialist Job Description The Small Scale Organics (SSO) Pilot Plant is a GMP (Good Manufacturing Practices) manufacturing facility ... in the Small Molecule Process Research and Development (SM PR&D) organization. The SSO...seamless technology transfer to commercial sites. The SSO Operations Specialist will provide hands on assistance for daily production… more
- Merck & Co. (Durham, NC)
- …and periodic 24 x 7 on-call support.Identify and implement process /equipment improvements and manufacturing efficiencies.Maintain technical documentation . ... Job DescriptionPosition Description: Senior Specialist , Manufacturing Automation The Senior Specialist Manufacturing Automation person is primarily responsible… 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 ... compliance with internal controls.Will review reconcile vendor statements and invoices, process all accounts payable transactions for payments, process 1099s,… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionPosition Description: Executive Transportation Specialist Working in a dynamic, fast paced environment, the Executive Transportation Driver reports ... Director, Executive & Personnel Protection, Global Security.The Executive Transportation Specialist is an experienced professional responsible for the safe 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 & ... process confirmation on shop floor. Relationships Manager, Quality Assurance....ISO standards, corporate & local SOPs Reviews & approves documentation for Quality approval - batch records & other… more
- Novo Nordisk Inc. (Durham, NC)
- …approval of Batch Production Records (BPRs), Change Requests (CR's), Deviations & other documentation (in conjunction with LoB) & QA presence & process ... to existing systems. Performs archiving duties & QA presence & process confirmation on shop floor. Relationships Manager, Quality Assurance. Essential Functions… more
- Aequor (New Brunswick, NJ)
- …degree required Duration: 6 months (possibility of extension)Job Description: Transportation Specialist This role is 100% Onsite, New Brunswick Work Schedule: Mon ... Summary/Overview of this role: Provide expertise and assist with the shipping process , logistics problem solving and carrier/vendor coordination to ensure that the… more
- Catalent (Manassas, VA)
- …to help create engaging new products consumers will love.The Document Control Specialist - 2nd Shift is responsible for creating and maintaining the Quality ... System documentation . Communicate any deviations to management. Assist the Quality...any other documents as required.Manage the routing and approval process for new documents and process deviations;… more
- Novo Nordisk Inc. (Durham, NC)
- …systems Support systematic problem solving related to equipment qualification Reviews documentation for accuracy & completeness Contribute to process ... functionality & life-cycle management a plus We commit to an inclusive recruitment process and equality of opportunity for all our job applicants. At Novo Nordisk… more
- Merck & Co. (Rahway, NJ)
- …Automation Engineer, you will play a crucial role in supporting the process automation systems within clinical manufacturing.-The Automation Specialist - ... life cycle documentation methodology for accurate and comprehensive documentation throughout the automation process .Keep automation systems validated and… more
- Catalent (Manassas, VA)
- …to help create engaging new products consumers will love.The Quality Assurance Specialist I - Quarantine is responsible for auditing the products and processes ... is a site based position.The Role: Responsible for managing the Quarantine process and for reviewing incoming materials' COAs; Manages and reviews incoming labels… 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
- 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 ... metrics data used to monitor the QC reviews, and may identify process improvementsAssist in educating, guiding and influencing the scientific staff in regard… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …CAR-T product manufacturing per inspection plan and record results to complete receipt process . Reviews inspection documentation (C of A or other Material ... Biotech is seeking a QA Warehouse Incoming Raw Material Specialist as part of the Quality team based in...manner in accordance with the procedures. Review and inspect documentation in support of Final Product Shipments. Generates inspection… more
- Aequor (Swiftwater, MN)
- …in a GMP setting MS Project experience Skills Proficiency in utilizing documentation system to author protocols and reports Experience participating in teams and ... Doc/GEODE&plus experience with a working knowledge of templates, workflows and approval process Strong root cause analysis with cGMP experience. Education BS/MS in… more
- Novo Nordisk Inc. (Durham, NC)
- …party instrument services Accurately & legibly records all activities in appropriate documentation . Writes work orders Reviews documentation for accuracy & ... instrument performance & responds to potential issues Contributes to process confirmations Maintains training qualifications on time. Supports training others… more
