- Merck & Co. (Rahway, NJ)
- …Supply (GCS) is responsible for developing and executing a systems and process automation strategy to support new and existing operations and supply technologies, ... analytics, reporting, and visualization capabilitiesDevelop and complete appropriate system validation , Change Control and testing documentation, ensuring compliance with… more
- Aptyx (Charlotte, NC)
- …engineer disposable medical devices from concept to production Hands-on products and process development of catheters and other disposable products Design devices in ... planning (project schedule, resources, budgets, etc.) Participate in the quotation process for projects Develop feasibility and reliability testing plans for… more
- Merck & Co. (Durham, NC)
- …Maintenance (PM) plans as requested. Responsible for SAP transactions, validation testing support, supporting root cause investigations and change control ... to perform routine maintenance tasks, work with and troubleshoot complex process systems, including but not limited to:Utility Equipment (eg boilers, chillers,… more
- Tris Pharma (Monmouth Junction, NJ)
- …(ARD) Scientist III, under guidance, performs laboratory analyses of raw materials, in process (IP), finished product (FP) and stability (ST) samples, as well as ... field and minimum 8 years' experience in analytical/method development or method validation in the pharmaceutical or biotechnology field OR Master's degree in… more
- Formation Bio (New York, NY)
- …Clinical Practices (GCP), Good Pharmacovigilance Practices (GPV) and Computer Systems Validation (CSV).The primary responsibilities for the Vice President of Quality ... there is a substantial component of oversight for the computer systems validation . The implementation of the QA strategy will involve leadership and guidance… more
- Merck & Co. (Durham, NC)
- …Maintenance (PM) plans as requested. Responsible for SAP transactions, validation testing support, supporting root cause investigations and change control ... Duties:Ability to perform routine maintenance tasks, work with and troubleshoot complex process systems, including but not limited to: Process Equipment (eg… more
- Bayer (Whippany, NJ)
- …service. The role combines digital expertise with the provisioning of process consultancy and guidance to cross-functional stakeholders related to their activities. ... to: Oversight of External Communication Procedure: Acts as LMR/PRT process owner and expert for the local organization, including...the intended use and configuration of AI. Reviews the testing/ validation of AI. Prepares an AI risk mitigation plan… more
- Cipla (Fall River, MA)
- …& product transfer by performing gap analysis to meet market requirements Review in- process analysis on daily basis to enhance the quality of final product Monitor ... to meet GMP by performing surprise checks Prepare and review the qualification, validation and other documents to maintain GMP Participate in the internal and… more
- Cipla (Fall River, MA)
- …Quality Team. The QA operation specialist (MDI) monitors and ensures validation and qualification of facility, utilities, equipment's, processes and ensure product ... quality is maintained throughout all phases of the manufacturing process in compliance with established specifications and standard operating procedures (SOPs) and… more
- Cipla (Central Islip, NY)
- …and validation activities as required. Apply complete knowledge of process improvement strategies and lean techniques (eg Method analysis, work combination ... Change Controls, Technical Deviations, Methods, Specifications, COAs, Batch Records, Validation protocols/reports. Conduct focused time-studies to support packaging operations.… more
