- Legend Biotech USA, Inc. (Raritan, NJ)
- …in the treatment of multiple myeloma.Legend Biotech is seeking QA Document Control Specialist I/II/III as part of the Quality team based in Raritan, NJ. Role ... OverviewThe QA Document Control Specialist role is an exempt level position with responsibilities...the periodic review process for proceduresIssuance of batch related documentation in support of GMP manufacturingReconcile GMP documentation… more
- Integra LifeSciences (Princeton, NJ)
- …patient outcomes and set new standards of care. The **Export Trade Compliance Specialist ** plays a critical role in ensuring full compliance with US Customs and ... exports. This position's focus will be classification and Country of Origin validation , and is responsible for validating, maintaining, and updating tariff codes… more
- Sun Pharmaceuticals, Inc (Princeton, NJ)
- …and compliance documents such as analytical methods, specifications, Method Validation /Transfer Protocols and Reports, SOPs accordingly to companys standards and ... Responsibility:** + Writes technical documents such as methods, specifications, method validation protocols and reports, method transfer protocols and reports based… more
- ATS Automation (Warminster, PA)
- …Industries Requisition ID: 15756 Location: Warminster, PA, US, 18974 Date: Oct 3, 2025 Validation and Documentation Specialist SP Industries Inc.is seeking a ... documentation or equivalent years of relevant experience. (Technical writing/ validation experience for pharmaceutical or biotechnology products preferred.) + One… more
- Insight Global (Hopewell Township, NJ)
- Job Description Our top Pharmaceutical client is seeking a Documentation and Validation specialist to join their External Call Center team within their ... a resource with IVR and Contact Center knowledge to spearhead documentation and validation of processes. The ideal resource will have experience with Salesforce… more
- ThermoFisher Scientific (New Brunswick, NJ)
- …background check, which includes a drug screening. The primary focus of the System Specialist role is to work as part of a team that provides business ownership ... Follow SOPs and industry best practices. + Author and/or review validation deliverables including requirement and design specifications, summary reports, pre/post… more
- CAI (Trenton, NJ)
- Product Support Specialist II **Req number:** R6406 **Employment type:** Full time **Worksite flexibility:** Hybrid **Who we are** CAI is a global technology ... Summary** We are looking for a motivated Product Support Specialist II ready to take us to the next...including complex "multi-quantity" entries that require multi-step procedures and validation + Mark and manage work-from-home (WFH) assets within… more
- Terumo Medical Corporation (Somerset, NJ)
- SAP Extended Warehouse Mgmt Specialist Date: Oct 1, 2025 Req ID: 4412 Location: Somerset, NJ, US, 08873 Company: Terumo Medical Corporation Department: SAP ... and tactical guidance of a Logistics and Warehouse Management Architect, the Specialist - SAP Extended Warehouse Management (SAP EWM) will collaborate with business… more
- Actalent (Princeton, NJ)
- …GMP documentation such as batch records, SOPs, test methods, validation protocols, and technical reports for accuracy and compliance. + Execute product-related ... Job Title: Quality Specialist Job Description We are seeking a dedicated Quality Specialist to join our dynamic team within a rapidly growing Cell and Gene… more
- Terumo Medical Corporation (Somerset, NJ)
- SAP FICO Specialist Date: Oct 1, 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
- Cardinal Health (Trenton, NJ)
- …development programs and regulatory submissions. **_Job Summary_** The Senior Regulatory Specialist , Data Management & Governance for Medical Devices plays a ... a dataset's origin, transformations, and access for regulatory reporting. + Support the validation of computer systems used for GxP data to ensure they comply with… more
- Integra LifeSciences (Plainsboro, NJ)
- …patient outcomes and set new standards of care. The **Quality Compliance Specialist ** will provide quality compliance support to the Collagen Manufacturing Center ... in the development, review and/or approval of various Quality System Documentation to ensure that the development, manufacture and distribution of medical… more
