- ATS Automation (Warminster, PA)
- …Requisition ID: 13624 Location: Warminster, PA, US, 18974 Date: Jan 12, 2025 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
- 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
- Merck (West Point, PA)
- …If so, we invite you to apply for the position of Manufacturing Automation Specialist at our West Point, PA site - the largest vaccine manufacturing facility in ... drug product process demonstration in support of facility licensure. The Specialist , Manufacturing Automation is responsible for supporting the process automation… 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
- Terumo Medical Corporation (Somerset, NJ)
- SAP CO Specialist , Record to Report Date: Dec 19, 2024 Req ID: 3975 Location: Somerset, NJ, US, 08873 Company: Terumo Americas Holding, Inc. Department: SAP ... go next!** **_Advancing healthcare with heart_** **Job Summary** The SAP CO Specialist , Record to Report will ensure a relationship with business stakeholders,… more
- Terumo Medical Corporation (Somerset, NJ)
- SAP FICO Specialist Date: Jan 13, 2025 Req ID: 3552 Location: Somerset, NJ, US, 08873 Company: Terumo Americas Holding, Inc. Department: SAP Leadership & COE Terumo ... **_Advancing healthcare with heart_** **Job Summary** The SAP FI-CO Specialist will collaborate with business stakeholders, cross-functional teams, external project… more
- Insight Global (Raritan, NJ)
- …system assessments, leveraging Tanium for deployment, performing testing and validation , maintaining documentation , providing training and support, ... Job Description Insight Global is hiring a Windows Migration Specialist with Tanium experience for a biopharmaceutical client located in Bridgewater, NJ. The Windows… 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
- Terumo Medical Corporation (Somerset, NJ)
- Camstar MES Design Specialist Date: Jan 14, 2025 Req ID: 2037 Location: Somerset, NJ, US, 08873 Company: Terumo Americas Holding, Inc. Department: SAP Leadership & ... ensure a successful release + Assist with user training documentation and training sessions + Responsible for quality, management...compliance + Familiar with FDA CFR Part 11 Software Validation processes + Keen analytical skills + Keen sense… 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
- 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
- Sanofi Group (Bridgewater, NJ)
- …protocol development (such as Informed consent, committees charters development), support to validation and clinical case review of study data, review of study plans ... the guidance of the CRD he/she collaborates with the Coding specialist , Biostatisticians, Data Managers, Global and Regional Study Managers, Feasibility Managers,… more
- AbbVie (Branchburg, NJ)
- …for the accurate and timely completion of production related cGMP documentation . Facilitates the transfer, planning, implementation, and maintenance of manufacturing ... + Monitors operator training files and work with compliance specialist to keep files up to date. + Works...see that work orders, dispensing, preventative maintenance, QC, and documentation issues are resolved and enhances communications at all… 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
- Nestle (Bridgewater, NJ)
- …* Effectively communicate project status and results through written technical documentation and oral presentations. * Preparation / review of PFD, P&ID's ... Utility sizing **Technical Assistance:** * Be recognized as a specialist in the field of Gummy Manufacturing and as...filling processes. * Experience in IQ, OQ, PQ and Validation processes * Good working knowledge on Statistical Process… more