for applications. Collaborate with the Systems Engineering Manager to establish best practices. Contribute systems input to tenders. Participate in system integration, project deliverables, and validation of technical documentation. Provide technical leadership to Systems Engineers. Support field operations by providing second-line product support. Attend business and technical briefings. Possess computer More ❯
CK Group are recruiting for a Quality Validation Specialist, to join a well-established and successful global pharmaceutical company, based in Hatfield, Hertfordshire, on a permanent basis. Role: This role is responsible for ensuring that electronic systems within the Quality Control Laboratory, and the Quality Systems operate in accordance with … of any associated quality policies, systems and procedures as required and prepare and update SOPs and training materials for system administration activities, Qualification and Validation activities. Support the maintenance and administration of the Electronic QMS. Support the effective management of the administration of QC laboratory system applications providing independence of … access for administrator activities. Ensure Qualification and Validation of equipment, processes, systems is/are performed in line with procedures, GMP and GAMP guidelines for process, equipment and electronic systems, as and when required. Ensure the maintenance of procedures supporting Qualification and Validation and review and approve Qualification and ValidationMore ❯
CK Group are recruiting for a Quality Validation Specialist, to join a well-established and successful global pharmaceutical company, based in Hatfield, Hertfordshire, on a permanent basis. Role: This role is responsible for ensuring that electronic systems within the Quality Control Laboratory, and the Quality Systems operate in accordance with … of any associated quality policies, systems and procedures as required and prepare and update SOPs and training materials for system administration activities, Qualification and Validation activities. Support the maintenance and administration of the Electronic QMS. Support the effective management of the administration of QC laboratory system applications providing independence of … access for administrator activities. Ensure Qualification and Validation of equipment, processes, systems is/are performed in line with procedures, GMP and GAMP guidelines for process, equipment and electronic systems, as and when required. Ensure the maintenance of procedures supporting Qualification and Validation and review and approve Qualification and ValidationMore ❯
