- Froedtert South (Kenosha, WI)
- POSITION PURPOSE Performs concurrent clinical documentation review to promote complete capture of documentation needed to accurately code level of clinical ... a Registered Nurse (RN) in the State of Wisconsin. CCS (Certified Coding Specialist ) preferred. KNOWLEDGE, SKILLS & ABILITIES REQUIRED Ability to read, write, hear,… more
- Integrated Resources, Inc (Waterloo, IA)
- Job Title: Documentation Specialist Location: Waterloo, IA 50613(Part Time) Duration: 1.5years contract (Possible Extension) Part-time, approximately 30 hours ... per week Job Description: As a Documentation Specialist , Engine Controls for Client Power...problem reports to assure adherence to PDP processes. . Review and verify work process steps performed by Software… more
- Labor-Solutions, LLC (Glendale Heights, IL)
- We are seeking a detail-oriented and organized Quality Document Specialist to join our team. The Quality Document Specialist will be responsible for ensuring the ... accuracy and completeness of all documentation is compliant. This position requires strong attention to...ability to work in a fast-paced environment. Responsibilities: - Review and verify and understand all documents for accuracy… more
- Novo Nordisk Inc. (Boulder, CO)
- …and scale-up processes from laboratory to pilot plant scale Author and/or review batch documentation and generate automated equipment methods Execute ... 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)
- …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)
- 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
- 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
- Merck & Co. (Durham, NC)
- …formulation vessel, lyophilizers, etc.).Provide QA shop floor support in the execution and review of GMP documentation such as IQ, OQ and other technical ... product inspection, and quality control laboratories. The Quality Assurance Specialist will support this expansion. Project activities requiring support include… 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...Quality Systems and Regulatory Manager in complete, appropriate detail; Review and verify the operators' paperwork to ensure they… more
- Merck & Co. (Rahway, NJ)
- …in supporting the process automation systems within clinical manufacturing.-The Automation Specialist - Engineering Auto Eng position will report to the Director, ... and develop appropriate system validation, change control, and testing documentation .Maintain familiarity with system life cycle documentation methodology… 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
- Exela Pharma Sciences, LLC (Lenoir, NC)
- …and other regulatory requirements are adhered to as it relates to review and approval of engineering/validation specific documentation . He/she must ensure ... The QA Specialist II - Engineering/Validation is responsible for cGMP...the Engineering and Validation departments. Job Responsibilities Perform Quality review /approval of URS, FAT, SAT, IQ,OQ,PQ protocols and summary… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …accurate and performed in a timely manner in accordance with the procedures. Review and inspect documentation in support of Final Product Shipments. Generates ... Biotech is seeking a QA Warehouse Incoming Raw Material Specialist as part of the Quality team based in...and record results to complete receipt process. Reviews inspection documentation (C of A or other Material Certifications) for… 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 ... ensuring compliance with internal controls.Will review reconcile vendor statements and invoices, process all accounts payable transactions for payments, process… more
- Novo Nordisk Inc. (Durham, NC)
- …Records (BPRs) & relevant quality processes are compliant with regulations. Performs quality review & approval of Change Requests (CR's) & other documentation ... compliance with Regulations, ISO standards, corporate & local SOPs Reviews & approves documentation for Quality approval - batch records & other documentation … 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 ... incoming labels and packaging materials and well as reviews receiving documentation . Responsible for maintaining Raw Materials and Finished Goods' Quarantine log;… more
- Novo Nordisk Inc. (Durham, NC)
- …Novo Nordisk and help us make what matters. The Position Performs quality review & approval of Batch Production Records (BPRs), Change Requests (CR's), Deviations & ... other documentation (in conjunction with LoB) & QA presence &...Handles release of raw materials & provides quality oversight, review & approval of validation activities associated with minor… more
- BioAgilytix (Durham, NC)
- …at BioAgilytix.Essential ResponsibilitiesPerform Quality Control (QC) technical, scientific, and compliance review of data and documentation generated by the ... OOS and OOT associated with Bioanalytical Operations data as applicableIssue QC review observations and work closely with the scientific staff to ensure data… more
- Blanchard Valley Hospital (Findlay, OH)
- PURPOSE OF THIS POSITION The primary purpose of the Professional Coding Integrity Specialist (PCIS) is to review , enter and/or modify charges as appropriate, ... including review of clinical documentation to ensure charge is supported and/or to determine...opportunities, and collaborate with RI Educator and/or Claims Resolution Specialist to avoid/reduce future edits. Support Condition 44 notifications… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …in the treatment of multiple myeloma. Legend Biotech is seeking a Metrology Specialist as part of the Maintenance & Metrologyteam based in Raritan, NJ. Role ... standards, parts and spare parts are identified and available. Performs work review , approval and close out of work orders, including management of third-party… more
