Senior Validation Manager - Princeton

The Senior Validation Manager is leading the site validation program and all qualification and validation activities at the Erytech, Princeton site. · ...

This job is for Lead/Manager Validation Engineer with experience of working in Life Sciences and Computer System Validation (CSV). The ideal candidate should have pharmacovigilance knowledge and hands-on experience of GAMP 5 Risk Based Validation, Functional Risk Assessment and D ...

We have an urgent opening for the position below. · Role - Senior Validation Manager · Location - Raritan, NJ(Hybrid) · ...

We are looking for a Sr Manager IT Clinical Systems Validation to help us expand what is possible for patients with serious diseases. · Reporting to the Director Clinical Systems Business Intelligence you will be responsible to provide the necessary expertise to validate and main ...

The specialist will execute Change and Release Management initiatives for Manufacturing Systems used in cell therapy products. · Responsible for technical and operational support for the Manufacturing Systems Change and Release Management activities. · Participates in developing, ...

We are looking for a CSV Validation/Compliance Test Manager to join our team for a permanent role. This role combines expertise in validation,data & analytics,Audit Readiness,and Business/Product Analysis-supported by strong capabilities in strategy,changenprocess improvement,and ...

Prior JNJ TQ Experience a must with 5+ years' experience in Computer System Validation (Based on the role selected) · ...

Dice es la plataforma líder de carrera para expertos en tecnología a todos los niveles de su carrera. Nuestro cliente, Shrive Technologies LLC, busca un gerente senior de validación. · Se requiere experiencia previa en JNJ TQ. · ...

We are looking for a Sr Manager IT Clinical Systems Validation in the IT team to help us expand what's possible for patients with serious diseases. · In this role you will have the opportunity to lead the planning execution and documentation of computer system validation CSV acti ...

Senior Validation Manager required for an urgent position at Ex-JNJ company. · ...

We are looking for a Sr Manager, IT Clinical Systems Validation in the IT team to help us expand what's possible for patients with serious diseases. · ...

Dice is the leading career destination for tech experts at every stage of their careers. · Prior JNJ TQ Experience a must · Experience in validating QMS and different modules in QMS · ...

At Insmed every moment and every patient counts and so does every person who joins in As a global biopharmaceutical company dedicated to transforming the lives of patients with serious and rare diseases you ll be part of a community that prioritizes the human experience celebrate ...

We are looking for a CSV Validation/ Compliance Test Manager to join our team for a permanent role. This role combines expertise in Validation, Data & Analytics, Audit Readiness, and Business/Product Analysis. · ...

+ 5+ years' experience with System Development Lifecyle + 10+ years' experience in Computer System Validation Experience in validating QMS and different modules in QSM Technology Quality representative and provide quality guidance from a CSV perspective based on the J&J CSV Frame ...

Sr Validation Manager for Long Term Contract at Raritan NJ. Requires prior JNJ TQ experience and 5+ years in System Development Lifecyle and Computer System Validation with FDA regulated environment GxP standards and Risk based validation. · ...

6+ years' experience in computer system validation. · Apply FDA, MHRA, and other applicable global health authority regulations to the development of computer systems. · FOLLOW SOPs AND industry best practices. · ...

Review and validate vendor-provided system documentation for serialization/track & trace systems (e.g., Optel, Systech, Trace Link) · ...

Apply FDA, MHRA, · and other applicable global health authority regulations to · the development of computer systems supporting regulated business processes. · ...

A Validation Specialist with 5+ years of experience in applying FDA, MHRA, and other global health authority regulations to computer systems supporting regulated business processes. · ...