13 Validation Jobs in Cheshire

new IT systems, software, and processes, the definition of new policies, governance frameworks, and ways of working, as well as the purchase, installation, and validation of new capital equipment. Role Scope Embedding Best Practices: Implement and promote project management best practices and governance standards to ensure the consistent and controlled more »

covers the management and execution of supply chain delivery of the systems including checking, and reviewing deliverables from internal and external sources, verification and validation, quality, time, and cost management.The individual will functionally manage any internal resources working within Workstreams, ensuring the deliverables are delivered to quality, time, and cost.The more »

develop, and test electronic systems and components for advanced diagnostic instruments and medical devices, using best practices and regulatory standards. Product processes, verification, and validation for product improvements. Ability to complete high level engineering change specs in the company database and defining change details for Engineering Change Orders Utilise CAD more »

Role: Engineering Change Manager Role Type: Temporary – 12 Months Location: Macclesfield - 100% On-Site Role Your New Company Working within the AstraZeneca UK Operations - Facilities Management Function, this position provides professional Engineering Subject Matter Expertise to support to the AstraZeneca more »

Quality team to enable the efficient evaluation and release of medicinal products Work closely and effectively with other departments such as Regulatory Affairs, Compliance, Validation, Sales, Logistics etc to the highest quality and compliance standards and maintaining product supply to market Act as Qualified Person to the business Host regulatory more »

Quality team to enable the efficient evaluation and release of medicinal products Work closely and effectively with other departments such as Regulatory Affairs, Compliance, Validation, Sales, Logistics etc to the highest quality and compliance standards and maintaining product supply to market Act as Qualified Person to the business Host regulatory more »

will play an important role in creating the high level design artifacts. You will also deliver high quality code deliverables for a module, lead validation for all types of testing and support activities related to implementation, transition and warranty. You will be part of a learning culture, where teamwork and more »

and softwaresupport, resolve breakdowns, implement preventative maintenance, and ensurecompliance with GMP (Good Manufacturing Practice), EHS, and company standards.Your role also involves supporting computer system validation, qualityimprovement initiatives, and training other team members. This is a hands-onrole where you'll collaborate closely with operations and engineering to ensurea safe and … software, and coding support to maintain system performance. Resolve equipmentbreakdowns and conduct root cause analysis. Ensure compliancewith GMP, EHS, and company standards. Support computersystem validation and lifecycle management. Contribute toengineering best practices and project execution. Train team memberson equipment, systems, and procedures. Automation Engineer, beneficial key skills, and experience: Engineering more »

covers the management and execution of supply chain delivery of the systems including checking, and reviewing deliverables from internal and external sources, verification and validation, quality, time, and cost management. The individual will functionally manage any internal resources working within Workstreams, ensuring the deliverables are delivered to quality, time, and more »

role also covers engagement with the supply chain, delivery of the systems including checking and reviewing deliverables from internal and external sources, verification and validation, quality management. The individual will also contribute to reporting requirements including ensuring any technical, safety and engineering risks are identified and escalated to the Lead more »

for the formulation and process development activities for Dechra's products across the CMC (chemistry and manufacturing controls), from early development studies to process validation, including support for technology transfer activities. To ensure that new product manufacturing and control processes are robust and reliable, it is critical that the appropriate … for GLP and GCP studies. Provides quality expertise in accordance with the global quality requirements in the creation of product characterisation, product specifications, method validation, stability and comparability assessments for technology transfers for veterinary medicinal products. Ensures quality expertise is provided in the various phases of the development process, including more »

pack at the pre-start hand-over meeting. * Co-ordinate remediation strategy and MMP approvals, EHO and NHBC/LABC conditions sign-offs and validation/verification reports. * Co-ordinate and manage all aspects of NHBC/LABC building control and warranty provision, and monitor compliance/discharge for CML … visits and check that the works carried out comply with the drawings, specifications and are to the required standards and that any testing or validation criteria has been satisfied. more »

of a Site Reliability Engineer: Maintain and enhance network monitoring, orchestration, and automation solutions, encompassing tasks such as inventory reconciliation, workflow automation, network configuration validation, health monitoring, alert management, and incident resolution. Conduct audits on Network Infrastructure to uphold best practices and standards. Work collaboratively with teams to troubleshoot and more »