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Interact with BPI partners to facilitate documentation review/exchange, advance project activities and attend project team meetings in absence of the Regulatory Project Lead, as needed. Under the direction of Regulatory Affairs management, participate in drug development from early stage development through final formulation, ensuring compliance with principles of Quality-by-Design, cGMP, and FDA rules and regulations.
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The Dayforce Workforce Management (WFM) Lead will focus on the system requirements for activity related to new WFM projects and ongoing review of existing configuration. Workday HRIS Experience.
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Ensure Equipment Compliance: Receive and review revisions to USP, EP, JP, FDA regulatory guidelines. Duties and Responsibilities Historical Performance Review: Execute the historical performance review (HPR), a periodic review of equipment performance and use.
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Maintains QMS and/or product certificates for the organization, including the retention, review, and posting of certificates, as well as fulfillment of internal and/or external requests for certificates.
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Timely review of all federal forms/attachments for filing of the Avaya federal consolidation. Review the Companys Income Tax account reconciliations on a quarterly basis. Review all federal pro-forma tax returns in Corptax and all applicable supporting workpapers.
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Troubleshoot by querying the database using SQL Management Studio to review stored values and/or using a text editor to manually review data files sent to Zelis by our Payer clients. Hiring remote at these locations - Morristown, NJAtlanta, GABoston, MASt Louis, MOSt Pete, FLPlano,TXUse advanced test editors and other technology tools to review X12 835 files for issues, to include but not limited to the following: Balance, structure, syntactical, data type and content errors; to develop and execute strategies to solve them.
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Review customer reliability, safety and maintainability requirements and provide RMS/C analysis. Generate reliability, maintainability and system safety reports for IPT and customer review.
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The methodology is designed to facilitate and ensure the achievement of quality, clinical and cost-effective outcomes and to perform a holistic and comprehensive admission and concurrent review of the medical record for the medical necessity, intensity of service and severity of illness.
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Experience with accounting software such as NetSuite or Sage Able to prepare, review and understand a financial statement. A not-for-profit family services company in Morris Plains, NJ is seeking a Bookkeeper who can handle all accounts payable and receivable, payroll, bank account management, and reconciliation tasks with ease.
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Timely review of all federal forms/attachments for filing of the company federal consolidation. Review deferred tax asset/liability work papers and balances. Review federal book-tax difference calculations.
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Confirm proper network performance Operational testing, verification, and acceptance: Run routine reports to review system operation Perform final inspection, testing and customer acceptance. RSS #LI-JM2 Hvac controls, building controls, building automation, programming, field technician, heating, ventilation, air conditioning, direct digital control, apogee, desigo, modbus, tridium, Niagara, alerton, controls, commissioning, lonworks, bacnet, ddc, bau, bms, building management, mechanical systems, system integration Equal Employment Opportunity Statement Siemens is an Equal Opportunity and Affirmative Action Employer encouraging diversity in the workplace.
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Review and update SAP HANA models and SAC reporting. review and update SAP HANA models and SAC reporting. Experience with S/4HANA on cloud and Core Finance modules (GL, CO, GR, AP, FA, CM and MM), Sub Ledger (FPSL) and SAC Planning and BI.Ability to optimize and troubleshoot the performance of SAP Analytics Cloud dashboards.
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The individual is expected to be able to function independently in the daily management of clinical research projects including the preparation/review of related key documents (i.e. protocols, Investigator’s Brochures, clinical study reports, summaries for regulatory submissions.
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Review and approve batch records, Apheresis, Aborted and Invalid Assays, etc. Write and/or review of Standard Operating Procedures (SOPs), as needed. The QA Associate will interact directly with site staff, who are performing the daily operational functions in support of their effort to produce quality products.
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Including but not limited to staff orientation prior to the beginning of the school year, program meetings, clinical seminars and case reviews when relevant, monthly meetings with the consulting psychologist, meetings with teacher, behaviorist and parents, monthly staff meetings, IEP meetings and Annual Review meetings (when indicated by supervisor) and all team meetings that are indicated by the individual needs of the student(s.
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