- Novo Nordisk Inc. (Plainsboro, NJ)
- …and analyzes contract terms and conditions of contracts. Ensures data in validation and rebate systems reflect the contract terms for accurate processing Reviews ... accurately and in a timely manner prior to data validation . Coordinates with external source for loading and scrubbing...ensure on time payment Provides support for ensuring all documentation for payments and contracts are filed and updated… more
- ATS Automation (Warminster, PA)
- …Requisition ID: 13624 Location: Warminster, PA, US, 18974 Date: Dec 14, 2024 Validation & Documentation Specialist ATS Scientific Products is seeking ... a full‐time Validation and Documentation Specialist in Warminster, PA to create and maintain various technical documents (eg, user manuals, equipment… more
- WuXi AppTec (Philadelphia, PA)
- …resource for the development, execution, review, and approval of Computerized Systems Validation , System Life Cycle Documentation ( Validation Plans, Design ... assessments, risk assessments, requirements traceability, URS, FDS, procedural mappings and Validation Project Plans. + Stay current with changes to GXP, including… more
- University of Pennsylvania (Philadelphia, PA)
- …wellness programs and resources, and much more. Posted Job Title Research Specialist C/D (Center for Cellular Immunotherapy) Job Profile Title Research Specialist ... C Job Description Summary The Human Genome Editing Research Specialist will play a key role in managing the...duties, the individual will contribute to the development and validation of standard operating procedures (SOPs) critical for modifying… more
- Merck (West Point, PA)
- …process design/definition, engineering studies, process demonstrations, change control and validation . + Prepare documentation to support regulatory submission ... looking to make a difference in vaccine manufacturing? As a Senior Specialist , you'll play a critical role in providing technical guidance, leading projects,… more
- Integra LifeSciences (Princeton, NJ)
- …patient outcomes and set new standards of care. The Sr. Regulatory Affairs Specialist is a seasoned senior professional role responsible for contributing to and ... regulations in the US, EU, Canada and globally. The Sr. Regulatory Affairs Specialist is responsible for providing advanced level regulatory input for regulatory … more
- Kelly Services (Fort Washington, PA)
- **Quality Assurance Specialist ** Kelly(R) Science & Clinical is seeking a **Quality Assurance Specialist ** for our client, a top consumer product company, in ... 12 months **Pay:** $33-35 an hour Depending on experience The QA Specialist is responsible for providing daily Quality Assurance support to the manufacturing… more
- Bank of America (Pennington, NJ)
- Sr Business Control Specialist - Consumer AML Operations Fort Worth, Texas;Pennington, New Jersey; Plano, Texas; Phoenix, Arizona **Job Description:** At Bank of ... as required by the BSA. _Position Summary:_ The Senior Business Control Specialist will provide oversight and support in executing internal control discipline and… more
- University of Pennsylvania (Philadelphia, PA)
- …programs and resources, and much more. Posted Job Title Cell Therapy Specialist (CVPF)(Center for Cellular Immunotherapy) Job Profile Title Cell Therapy ... Specialist Job Description Summary This position carries out day-to-day...Aseptic cell processing following established Standard Operating Procedures. Accurate documentation following Good Documentation Practices. Prepare cell… more
- NTT America Solutions, Inc. (Trenton, NJ)
- …and thrive. **Your day at NTT DATA** The role of Telecommunications Specialist has the core responsibility of acquiring and processing orders for telecommunications ... to carrier. + Creates Purchase Request to Finance for ordered services and updates documentation with PO; updates invoices so POs show up properly in invoices. +… more
- Penn Medicine (Philadelphia, PA)
- …your life's work? Pathology (Genomics) Full Time- Day Shift The Genomic Development Specialist performs a vital role in developing new clinical assays in the ... Division of Precision and Computational Diagnostics (PCD). The Development Specialist will work closely with a team of laboratory professionals to design and perform… more
- Novo Nordisk (Plainsboro, NJ)
- …Reviews and analyzes contract terms and conditions of contracts. Ensures data in validation and rebate systems reflect the contract terms for accurate processing + ... accurately and in a timely manner prior to data validation . Coordinates with external source for loading and scrubbing...on time payment + Provides support for ensuring all documentation for payments and contracts are filed and updated… more
- Highmark Health (Trenton, NJ)
- …and Medicaid Services (CMS) coding guidelines, and Risk Adjustment Data Validation (RADV) Audits. Works closely with physicians, team members, Quality, Compliance, ... projects to comply with all CMS requirements by analyzing physician documentation and interpreting into ICD10 diagnoses and HCC disease categories. Supports… more
- M&T Bank (Cherry Hill, NJ)
- …for specific customer entity structures; customer signatures must match legal documentation . Leverage appropriate websites to perform validation and confirm ... accounts. Responsible for understanding commercial deposit accounts to include legal documentation , systems, and the servicing of customer needs. Serves as the… more
- Endo International (Horsham, PA)
- …from the local, contract manufacturing, filling, and packaging facilities. Quality Documentation /Reports Review + Contributes to preparation and/or review of annual ... that require developing options to solve moderate to complex issues. Quality Documentation + Prepares and/or reviews controlled documents (eg SOPs) required for… more
- PCI Pharma Services (Philadelphia, PA)
- …for the Philadelphia facility. This Quality Management System includes Documentation Control, Investigation and CAPA Management, Training, Internal/External Audits, ... Customer Correspondence, Validation . This position reports to the Senior Training Manager,...documents include SOP's, forms, regulatory documents etc. Wherever possible, documentation best practices should be applied consistently across the… more
- Integra LifeSciences (Plainsboro, NJ)
- …status of all documents. + Maintains hard copies of all approved documentation . + Maintains appropriate templates for access. + Tracking, follow-up, and ... including but not limited to, ECRs, DCRs, ECOs, DCOs, and MCOs.deviations, validation records, batch records, and notebooks. + Responsible for processing change… more
- Integra LifeSciences (Plainsboro, NJ)
- …employees at CMC. This role works closely with the Sr. Training Specialist assisting in the development of training materials, coordinating and delivering training ... GDP training. + Supports training management system enhancement activities and validation efforts. + Provides support during regulatory inspections by assisting with… more
