Head of Quality Systems Validation - Hillsboro

This role involves end-to-end system software architecture for a specific technology or market segment. The candidate will provide technical direction for software development and validation, engage with customers on technical requirements and interact with technologists to evalu ...

We are seeking a System Validation Architect to join our team. The successful candidate will be responsible for architecting end-to-end system software for a specific technology, product/platform, or market segment. They will also engage with customers on technical requirements/d ...

Job summary · Genentech's Hillsboro Oregon campus—Hillsboro Innovative Therapies (HIT)—serves as a critical hub for emerging cell & gene therapy manufacturing. · ResponsibilitiesArchitecting and leading a scalable Quality Systems and Validation roadmap and strategy aligned with c ...

As the Head of QSV you will serve as a pivotal strategic architect designing and orchestrating a world-class QSV framework for cutting-edge high-throughput GMP manufacturing facility. · ...

We are seeking an experienced IT/OT Computer Systems Validation (CSV) Engineer to support regulated manufacturing systems within a GMP pharmaceutical environment. · ...

This role is a part of our Quality Systems and Validation (QSV) team, which is dedicated to supporting the design, startup, and operation of a cutting-edge GMP facility. · ...

+This role is part of our Quality Systems and Validation (QSV) team which supports design startup and operation of cutting edge GMP facility. · +Architecting and leading scalable quality systems validation roadmap strategy aligned with cGMP regulations project milestones. · ...

We're looking for a Software Engineer to join our Data Center Performance Engineering and Competitive Marketing team. · ...

We are shaping the future of technology to help create a better future for the entire world. Our work in pushing forward fields like AI, analytics, and cloud-to-edge technology is at the heart of countless innovations. You'll have the opportunity to use technology to power major ...

We are seeking an experienced MES Validation Engineer to support the multi-phase deployment and validation of Manufacturing Execution Systems (MES) within a regulated manufacturing environment. · Ensure all validation activities comply with applicable regulatory requirements and ...

The MES Validation Engineer will support the deployment and validation of Manufacturing Execution Systems (MES) in a GMP environment. · Develop, draft and route for approval overall test scripts, validation protocols and their associated reports for computer systems. · ...

This position involves developing test scripts validation protocols reports computer systems regulatory industry standards. · ...

We are seeking a Validation Engineer II – CSV & Compliance to support IT/OT system owners with computer system validation (CSV), lifecycle documentation, compliance reporting, · and ongoing system maintenance for GMP-regulated manufacturing systems (ISA-95 Level 2 & 3). The ideal ...

MES Validation Engineer role overview: BEPC seeks an experienced MES Validation Engineer to support Manufacturing Execution System (MES) deployment at an innovative therapies manufacturing site in Hillsboro, OR. · ...

We are seeking an experienced MES Validation Engineer to support the multi-phase deployment and validation of Manufacturing Execution Systems (MES) within a regulated manufacturing environment.This role will focus on ensuring computerized systems are validated in compliance with ...

You will play a crucial role in supporting the multi-phase deployment of MES. · ...

The Hillsboro Innovative Therapies team at Client is at the forefront of bringing new medical advancements from development stages to commercial manufacturing. · Develop, draft and route for approval overall test scripts, validation protocols and their associated reports for comp ...

The Validation Engineer II will support Computer System Validation (CSV) and compliance activities for regulated IT/OT manufacturing systems. · Bachelor's degree in Computer Science, Engineering, Life Sciences, or a related field. · 5+ years of experience in Computer System Valid ...

Bring state of the art automation technology to our site, optimizing our ability to serve patients efficiently. · Develop overall test scripts and validation protocols for computer systems ensuring compliance with regulatory and industry standards. · Work collaboratively with ITO ...

We are seeking a Validation Engineer II to support Computer System Validation (CSV) and compliance activities for IT/OT systems in a GMP-regulated manufacturing environment. · Support IT/OT System Owners across the full lifecycle of computerized systems. · Create CSV lifecycle do ...