Computerized Interlocking Systems - 21+ job offers

TITLE: Principal GxP Computerized Systems Engineer DEPARTMENT: Operations REPORTS TO: Associate Director Professional Service Operations CLASSIFICATION: Exempt (salary) STATUS: Full Time LOCATION: Varies Between Remote and at a Client Site cGMPnow accelerates Next Generation Therapies to patients by

Bora Pharmaceuticals is a premier international contract development and manufacturing organization (CDMO) specializing in formulation development, clinical and commercial manufacturing, and packaging of complex oral solid dose, liquid, semi-solid, biologics, and sterile injectable pharmaceutical pr

An established industry player is seeking a Validation Specialist for Computerized Systems to ensure compliance with GxP standards. In this pivotal role, you will be responsible for performing initial and routine validation activities, including qualification of laboratory instruments and troublesho

A leading CDMO based in Minneapolis is seeking a Validation Systems Specialist to support computerized systems validation in pharmaceutical manufacturing. You will work closely with business units to establish requirements, prepare comprehensive validation documentation, and ensure compliance with r

An established industry player is seeking a Senior Validation Specialist to oversee validation activities for GxP computerized systems. This role involves qualifying laboratory instruments, troubleshooting system issues, and ensuring compliance with industry standards. The ideal candidate will have

Bora Pharmaceuticals

SUMMARY This position is responsible for establishing and maintaining the validated state for software-based computerized systems in use at Bora Pharmaceuticals Inc. according to the Validation Policy for Computerized Systems and in compliance with FDA and other regulatory requirements. ESSENTIAL FU

The field of gene therapy is growing rapidly and Genezen is here to meet the exacting needs of our clients. We provide process development, produce GMP viral vectors, and provide cell transduction for gene and cell therapy clinical trials and are proud to be a part of the process that leads to new c

Computer Systems Validation Specialist page is loaded## Computer Systems Validation Specialistlocations: Maple Grove, MNtime type: Full timeposted on: Posted Todayjob requisition id: 9484**SUMMARY**This position is responsible for establishing and maintaining the validated state for software-based c

Computerized Maintenance Management Systems (CMMS) Coordinator II Location: Portsmouth, NH. The shift schedule is from 8am-4:30pm: Monday - Friday. Overtime pay and annual bonus opportunity are available. A Computerized Maintenance Management Systems (CMMS) Coordinator II is Responsible for complex

TechDigital Group

An established industry player is seeking a Validation Specialist for Computerized Systems to ensure compliance with GxP standards. In this pivotal role, you will be responsible for performing initial and routine validation activities, including qualification of laboratory instruments and troublesho

TechDigital Group

An established industry player is seeking a Senior Validation Specialist to oversee validation activities for GxP computerized systems. This role involves qualifying laboratory instruments, troubleshooting system issues, and ensuring compliance with industry standards. The ideal candidate will have

BWX Technologies

Position Overview: Establishing GMP applications to digitize quality and manufacturing systems. Supporting the development, maintenance and lifecycle management (LCM) of new GMP computerized systems. Maintenance and LCM of established GMP digital systems. Location: On-site in Kanata, Ontario Your Da

BWX Technologies

Position Overview: Establishing GMP applications to digitize quality and manufacturing systems. Supporting the development, maintenance and lifecycle management (LCM) of new GMP computerized systems. Maintenance and LCM of established GMP digital systems. Location: On-site in Kanata, Ontario Your Da

Strong QA oversight experience in computerized systems validation (CSV) and remediation initiatives Hands on expertise with periodic reviews Solid working knowledge of FDA Computer Software Assurance (CSA) principles, and a track record of ensuring compliance in regulated environments. Knowledge of

The field of gene therapy is growing rapidly and Genezen is here to meet the exacting needs of our clients. We provide process development, produce GMP viral vectors, and provide cell transduction for gene and cell therapy clinical trials and are proud to be a part of the process that leads to new c

Computerized Maintenance Management Systems (CMMS) Coordinator II Location: Portsmouth, NH. The shift schedule is from 8am-4:30pm: Monday – Friday. Overtime pay and annual bonus opportunity are available. A Computerized Maintenance Management Systems (CMMS) Coordinator II is Responsible for complex

The field of gene therapy is growing rapidly and Genezen is here to meet the exacting needs of our clients. We provide process development, produce GMP viral vectors, and provide cell transduction for gene and cell therapy clinical trials and are proud to be a part of the process that leads to new c

Bristol Myers Squibb

*Working with Us** Challenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest bre

SUMMARY This position is responsible for establishing and maintaining the validated state for software-based computerized systems in use at Bora Pharmaceuticals Inc. according to the Validation Policy for Computerized Systems and in compliance with FDA and other regulatory requirements. ESSENTIAL FU

*SUMMARY** This position is responsible for establishing and maintaining the validated state for software-based computerized systems in use at Bora Pharmaceuticals Inc. according to the Validation Policy for Computerized Systems and in compliance with FDA and other regulatory requirements. *ESSENTIA