Stevenage, Hertfordshire, South East, United Kingdom
Russell Taylor Group Ltd
tasks related to pharmaceutical products. Ensuring products are fit for purpose before release for use or commercial sale. Maintaining and improving QMS' performance by ensuring items such as deviations, CAPAand change control for which you are the owner are progressed in a compliant and timely manner and all other items are reviewed and/or approved in accordance with … hold a degree in a STEM related subject Experienced in batch review and batch release GMP QA experience is essential! Ideally in a Pharmaceutical setting or similar Experience in CAPA, deviations, change controls, internal auditing (preferred) etc Strong interpersonal skills, we are looking for Candidates who are good communicators Strong written and verbal use of English language essential due to More ❯
primary contact with regard to Quality performance Administer the Fault Analysis Reporting process and ensure that the reports are distributed to management and monitor the completion of the correctiveandpreventiveaction of each entry. Manage the internal and external audit process and assist with audits where appropriate and/or necessary. To ensure that the Quality Systems are harmonised More ❯
Leighton Buzzard, Bedfordshire, South East, United Kingdom
1TECH STAFFING LIMITED
and ensuring compliance with EU GDP guidelines. Key Responsibilities: Maintaining and enhancing the QMS to meet regulatory, ISO, and client requirements. Supporting audits (regulatory, ISO, client, supplier) and managing CAPA plans. Driving a culture of quality excellence across the business. Conducting supplier audits, internal inspections, and management reviews. Key Requirements: Proven experience in a GMDP or similar regulated environment. Strong More ❯
Provide technical support for customer and product investigations, defect resolution, lifecycle maintenance, and feature enhancements. Process and Documentation: Contribute to software process controls, design documentation, risk management activities, andCAPA processes. Requirements and Architecture: Translate customer and business requirements into robust embedded systems and software architectures aligned with product goals. Technical Analysis: Interpret technical documentation such as circuit diagrams andMore ❯
to recommend service improvements. Work with ITSM teams to ensure accurate SLA tracking and OLA performance reporting within ServiceNow. Support the definition and implementation of correctiveandpreventive actions (CAPA) based on insights. Develop and manage automated and custom reports from ServiceNow Performance Analytics, ServiceNow Reporting, and other BI platforms (e.g., Power BI) Create real-time dashboards to monitor IT More ❯
to recommend service improvements. Work with ITSM teams to ensure accurate SLA tracking and OLA performance reporting within ServiceNow. Support the definition and implementation of correctiveandpreventive actions (CAPA) based on insights. Develop and manage automated and custom reports from ServiceNow Performance Analytics, ServiceNow Reporting, and other BI platforms (e.g., Power BI) Create real-time dashboards to monitor IT More ❯
Engineer include: Collaborate with the production team to ensure the conformance of goods and sample inspection of manufactured products. Lead problem-solving efforts to identify root causes and complete CAPA (CorrectiveandPreventive Actions). Manage customer returns processes, including root cause analysis andcorrective actions, ensuring timely resolution of customer issues. Evaluate processes and make continuous improvements, implementing new More ❯
Basingstoke, Hampshire, South East, United Kingdom
Orion Electrotech Manufacturing
Engineer include: Collaborate with the production team to ensure the conformance of goods and sample inspection of manufactured products. Lead problem-solving efforts to identify root causes and complete CAPA (CorrectiveandPreventive Actions). Manage customer returns processes, including root cause analysis andcorrective actions, ensuring timely resolution of customer issues. Evaluate processes and make continuous improvements, implementing new More ❯
High Wycombe, Buckinghamshire, England, United Kingdom
Cpl Life Sciences
research into new materials and capabilities for future product developments Diagnose product complaints received, identifying the root causes of any problems. Systematically capture all analysis and resultant actions in CAPA system. Write and manage all inputs and analyses required for the Company’s technical files, working closely with the Company’s regulatory consultant. Work with Manufacturing to identify and evaluate More ❯
levels to ensure traceability. Identify, segregate, and document non-conforming products, and support Quality and Operation teams to resolve quality issues. Assist in root cause investigations and support correctiveandpreventiveaction processes. Maintain a clean and organised inspection area maintaining appropriate H&S standards. Update the company’s ERP system with accurate and timely quality data, including inspection results More ❯