- 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
- Sokol Materials & Services (Skillman, NJ)
- CQV Technical Writer / Validation Engineer Apply Now (https://forms.monday.com/forms/3cdf5bfb73703e4a3aa29c55653510f4?r=use1) Job Type Validation Engineer ... at times. About the Role As a Technical Writing Specialist at Sokol GxP Services, you will play a...the creation of technically accurate documents in line with validation programs. - Process-oriented with strong critical thinking and… more
- J&J Family of Companies (Titusville, NJ)
- Johnson & Johnson is currently recruiting for Equipment Lifecycle Management (ELM) Specialist ! This position will be located in Titusville, NJ. At Johnson & Johnson, ... at https://www.jnj.com/. Position Summary: The Equipment Lifecycle Management (ELM) Specialist performs the technical execution of ELM Quality Control activities… 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
- 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
- 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: Dec 15, 2024 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
- 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
- Terumo Medical Corporation (Somerset, NJ)
- Camstar MES Design Specialist Date: Dec 16, 2024 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
- Merck (West Point, PA)
- …Projects, Maintenance, Safety, Process Development, Technical Services, Utilities and Qualification/ Validation . This position is a support role for utility systems ... design, and supports commissioning and start-up activities ranging from documentation to equipment inspection. + Optimizes equipment maintenance activities including… more
- Eurofins (North Brunswick Township, NJ)
- …+ Audits various reports prior to issuance (eg analysis reports, method validation reports, research and development reports (as needed), special project reports, ... for all quality inquiries on analytical reports and related documentation . + Audit methods, work instructions, deviations, investigations, corrective actions,… 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
- AbbVie (Branchburg, NJ)
- …personnel in the production of clinical or commercial products. By ensuring accurate documentation and adherence to cGMP standards, you will play a vital role in ... + 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
- 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