Our client has an opportunity for a Quality Manager to join them on a contract basis until the end of 2025 with the potential for extension. You will be managing and delivering Process Assurance tasks and deliverables. Role : Quality Manager - Process Assurance of Systems development Location : Filton - 60% onsite per week Hours : 35 per week Clearance : BPSS required … deployment of relevant processes. Review and provide feedback on planning activities, including related documentation, to secure deployment of applicable processes for the system development. Perform detailed validation and verification quality checks across the lifecycle of the system development Systems and Software Engineering - System Life Cycle Processes, ISO/IEC/IEEE 15288 and document results; such as: Check completeness … of requirements cascade and their correct definition. Check applicability of verification results with respect to requirement validation. Check effectiveness of the management of potential non-compliances. Perform detailed documentation quality checks, for some of the system development deliverables, and document results. Attend and support process assurance meetings by presenting results of quality checks and defining recovery actions. More ❯
Quality Assurance (QA) Validation- Contract Role (Sterile Pharma, Swindon - Onsite) Your new company A leading pharmaceutical organisation specialising in sterile manufacturing is seeking a skilled QA Validation expert to support a high-impact project. With a strong commitment to quality and regulatory compliance, this company offers a dynamic and collaborative environment for experienced contractors. Your new role As … a Quality Assurance QA Validation Expert, you will serve as a Document Reviewer for Commissioning, Qualification, and Validation (CQV) activities. You'll be responsible for reviewing technical documentation related to equipment used in sterile pharmaceutical manufacturing, ensuring alignment with cGMP, FDA, and EMA standards. You'll collaborate with cross-functional teams to identify gaps, recommend corrective actions, and support … continuous improvement efforts. What you'll need to succeed Experience in a quality assurance validation role within sterile pharmaceutical manufacturing Strong knowledge of FDA, EMA, and cGMP regulations Exceptional attention to detail and analytical skills Proficiency in document management systems and qualitymanagement software Excellent communication skills and the ability to work independently Familiarity with risk More ❯
Quality Assurance (QA) Professionals – Construction, Mechanical, and Electrical Devonport Docks, Plymouth (Hybrid) 12 Months Initially Rate: Competitive + expenses We are currently recruiting on behalf of a Tier 1 subcontractor working on the prestigious Devonport Docks Project in Plymouth. As part of this major infrastructure programme, we are seeking experienced Quality Assurance professionals with backgrounds in construction, mechanical … or electrical disciplines. Key Responsibilities: • Conduct quality inspections and audits across a range of disciplines (civils, M&E). • Ensure compliance with project specifications, industry standards, and safety regulations. • Maintain detailed QA documentation, inspection reports, and records. • Liaise with site teams, subcontractors, and client representatives to resolve quality issues. • Support the development and implementation of project-specific quality … a QA role within a construction, mechanical, or electrical setting. • Familiarity with QA processes and procedures on large-scale infrastructure or defence projects. • Strong understanding of industry standards and quality systems. • CSCS card and relevant qualifications in your discipline (e.g. NVQ, HNC/HND, or equivalent). • SC clearance or willingness to undergo security clearance (due to the nature More ❯
