1 to 25 of 260 Permanent QMS Jobs

have a wide range of responsibilities, from operational tasks like batch review and production liaison to broader activities such as auditing, supplier management, and QMS implementation. Crucially, you'll also serve as Deputy QA Manager, with some immediate line management duties and close collaboration with the QA Manager to meet more »

JIRA and Confluence, ERPs, etc. Desirable • Knowledge of using Agile/Scrum for delivering work packages • Experience of working within an ISO 9001 Quality Management System • A formal Project Management qualification (e.g. PRINCE2, MSP, PMQ, etc more »

of the relevant regulations Provide reports to management to enable them to monitor system performance. Review and authorise documentation and processes in the Quality Management System to ensure compliance with established quality procedures and applicable regulations and alignment with other related documentation. Identify and collaborate in the implementation of changes more »

in a licensed GMP facility. Experience of specification and monitoring of environment/equipment/products relevant to radiopharmacy. Experience of maintaining a Quality Management System, including change control, investigation of errors and deviations. Experience of managing staff. Experience of personal career involvement in operational management of radiopharmacy service provision more »

Infrastructure, Manufacturing, Chemical, Education and Training, Healthcare, Pharmaceutical, IT, Finance, HR and Support Services markets. We offer this service through the Ten Live Quality Management System which has combined our 60 years + experience in the industry, our partnerships with industry bodies and regulators and a customer-centric quality management more »

throughout our business and ensure we deliver the optimum level of efficiency whilst maintaining the highest quality standards and continuous improvement of our quality management system ISO 9001:2015. We aim to minimize environmental impact of our own systems and help develop environmentally responsible customer solutions. DPS Group recognises its more »

for improvement. Collaborate with manufacturing engineers on customer requirements to ensure compliance within the Production environment. Assist in general Upkeep & continual improvement of the QMS to ensure compliance to EN9100. Develop inspection and risk management methods to analyse product quality inline with customer requirements such as MSA, FMEA, CPK. Perform more »

or maintaining and archiving documentation Supporting and executing external audits where applicable Supporting management when hosting regulatory audits Working on executing and maintaining the QMS, including but not limited to: Risk Assessments Change Controls CAPAs Deviations Complaints Recalls OOS/OOT The Person: Will have a Degree in a relevant more »

management and loss prevention initiatives in order to safeguard pharmaceutical products, streamline operations, and minimise risks. KEY RESPONSIBILITIES Develop and oversee a robust quality management system in line with pharmaceutical industry regulations, including Good Distribution Practices (GDP) and Good Manufacturing Practices (GMP). Establish quality policies, procedures, and guidelines to more »

responsibilities will be: Develop and implement quality assurance policies, procedures, and standards specific to defence and naval systems. Establish and maintain a comprehensive quality management system to ensure consistent product quality and reliability. Lead and manage a team of quality assurance professionals, providing guidance, training, and support as needed. Collaborate more »

responsibilities will be: Develop and implement quality assurance policies, procedures, and standards specific to defence and naval systems. Establish and maintain a comprehensive quality management system to ensure consistent product quality and reliability. Lead and manage a team of quality assurance professionals, providing guidance, training, and support as needed. Collaborate more »

the development and validation of biomarker assays and Precision Medicine Solutions. Facilitate/participate in projects to deliver improvements to the clinical laboratory Quality Management System through collaboration with R&D Understand the business needs of PM departments, with respect to technology infrastructure, third party work and human biological sample more »

Infrastructure, Manufacturing, Chemical, Education and Training, Healthcare, Pharmaceutical, IT, Finance, HR and Support Services markets. We offer this service through the Ten Live Quality Management System which has combined our 60 years + experience in the industry, our partnerships with industry bodies and regulators and a customer-centric quality management more »

that all costs are considered. Providing routine internal commercial and progress reporting in accordance with management time requirements Maintain systems to see that Quality Management System ISO 9001 and 14001 are implemented. Progress all sales opportunities. Develop and pursue new and existing sales leads Ensure No Claims are made on more »

or Quality Manager or Quality Management experience gained within a software development working environment. Experience of ISO9001:2015 quality standard and maintaining a Quality Management System Any knowledge or experience of ISO27001/002 or maintaining an Information Security Management System would be advantageous but not essential. Experience of developing more »

or Quality Manager or Quality Management experience gained within a software development working environment. Experience of ISO9001:2015 quality standard and maintaining a Quality Management System Any knowledge or experience of ISO27001/002 or maintaining an Information Security Management System would be advantageous but not essential. Experience of developing more »

related meetings. Maintaining the divisions central quality and service management documents, which includes conducting regular reviews and updates to policies and procedures. Maintaining the QMS and SMS risk and action logs. Liaising with external and internal auditors, including issuing and reviewing audit reports, maintaining audit finding logs, and proactively following more »

Quality Agreements and GMP guidelines. Serve as the QA representative on the Site Leadership Team. Lead adherence to local or corporate Quality Management Systems (QMS). Collaborate in developing the Quell PQS, including implementing an eQMS where applicable. Define and develop new quality processes, policies, and data management systems. Establish more »

facilities in the UK and abroad Adhere to all company policies, procedures and business ethics codes including anti-bribery policy and Environmental and Quality Management System, compliant with ISO standards PERSON SPECIFICATION Required experience Experience of working in a similar technical engineering role related to electrical networks, solar, battery storage more »

Preparation and approval of validation documentation or management of the process (fulfilling the Quality Assurance role) in accordance with the relevant processes (e.g. Quality Management System) To monitor project and/or support activities to ensure systems are fit for purpose, that significant risks are identified and mitigated, and that more »

throughout our business and ensure we deliver the optimum level of efficiency whilst maintaining the highest quality standards and continuous improvement of our quality management system ISO 9001:2015. We aim to minimize environmental impact of our own systems and help develop environmentally responsible customer solutions. DPS Group recognises its more »

throughout our business and ensure we deliver the optimum level of efficiency whilst maintaining the highest quality standards and continuous improvement of our quality management system ISO 9001:2015. We aim to minimize environmental impact of our own systems and help develop environmentally responsible customer solutions. DPS Group recognises its more »

expert who is fully versed with Samsung processes and platforms 10+ years of experience in Project management/Vendor Management with good knowledge in QMS systems HOURS OF WORK: 37.5 hour week. Some weekend and evening work may be required for emergencies and projects. CHALLENGE: We are operating in a more »

many different tasks on a day to day basis. These will involve: - Working with the Accountable Pharmacist to ensure effective operation of the quality management system - Liaising closely with the Specialist radiopharmacy Technicians supporting the management of the workload, ensuring the unitis fully functional - Working closely with the Accountable Pharmacist more »

IT systems at an advanced level, e.g. MS Office and Project, Atlassian JIRA and Confluence, etc. Experience of working within an ISO 9001 Quality Management System, or similar, is desirable. The above list outlines our ideal candidate, but we know some of you may not apply unless you qualify for more »