Director, Commissioning, Qualification, and Validation

The Qualification Validation Specialist serves as a Subject Matter Expert (SME) for the Qualification Validation Management (QVM) function within the Quality Assurance (QA) department. · Servir como un experto en materia para el manejo de la validación y calificación dentro del d ...

We are seeking a proactive and detail-oriented CQV Engineer to support our client's pharmaceutical and life sciences projects in Raleigh. · ...

Responsible for supporting validation and qualification activities throughout the full equipment and system lifecycle ensuring compliance with regulatory and quality standards. · ...

Johnson & Johnson is searching for a Senior Commissioning Qualification Validation Engineer to join their team in Spring House PA. · Ownership for the development and execution of the Project Validation Master Plan PVMP · Support the writing and approval of URSs User Requirement ...

We are searching for the best talent for a Senior Commissioning, Qualification, and Validation (CQV) Engineer to join our Team in Spring House, · Pennsylvania. This position is part of the Site Engineering Team, · which is responsible for commissioning and qualification of equipm ...

This infrastructure qualification validation engineer role involves working with clients to deliver high-performance results based on their unique requirements. · ...

The Director of Commissioning Qualification and Validation CQV/CSV projects while driving business development initiatives This role manages a team of senior junior resources focusing on project execution building nurturing client relationships to promote Kymanox services · ...

+Job summary · CAI is a professional services company established in 1996 that has grown year over year to nearly 800 people worldwide. For Mission Critical and regulated industries that need to deliver critical solutions in high-stakes environments, we provide accelerated operat ...

The Global Director of Commissioning will drive business growth in commissioning qualification & validation inclusive of equipment facilities computer process and cleaning validation. · This role requires organization systems-thinking establishment of norms in service delivery an ...

The Validation Engineer supports the successful implementation of laboratory equipment and systems at multi-use sites through interaction with internal customers and external service providers. · ...

We are seeking a visionary Solution Qualification & Validation (SQV) Architecture and Governance Manager to be the chief architect of our end-to-end user journeys. · ...

We are seeking a visionary Solution Qualification & Validation (SQV) · Architecture and Governance Manager to be the chief architect of our end-to-end user journeys. · ...

We are seeking a skilled Validation Engineer to perform the full qualification of a cold room (2-8°C) for a regulated FDA production site. · ...

We are seeking a talented dedicated individual committed to work under the highest ethics standards for the following position Qualification Computer System Validation CSV Scientist. · ...

We are seeking a skilled Validation Engineer to perform the full qualification of a cold room (2-8°C) for a regulated FDA production site. · ...

Validation & Engineering Group, Inc. (V&EG) is a leading services supplier who provides solutions for the Pharmaceutical industries. · ...

We are seeking a skilled Validation Engineer to perform the full qualification of a cold room (2-8°C) for a regulated FDA production site. · ...

We are seeking a skilled Validation Engineer to perform the full qualification of a cold room (2-8°C) for a regulated FDA production site. · ...

We are seeking a skilled Validation Engineer to perform the full qualification of a cold room (2-8°C) for a regulated FDA production site. · ...

We are seeking a talented Validation Engineer to perform the full qualification of a cold room (2-8°C) for a regulated FDA production site. · Bachelor's degree in Engineering, Life Sciences, or related field. · 3+ years of validation experience in GMP-regulated environments. · ...