1 to 25 of 281 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 »

sites. In this role you will be key in the following areas… • Providing review and approval of validation lifecycle documents from a variety of QMS within the company. Provide meaningful comments to ensure compliance with regulatory expectations/requirements. • Provide quality oversight of internal business groups and external services partners more »

You will be required to support the Head of QA, responsible person and responsible personfor import, in the implementation and maintenance of the Quality Management System in accordance with ISO 9001 and ISO 13485 standards, and in compliance with EU GDP guidelines. Ideally you will have experience of working in more »

or exceeding of SLAs and KPIs. Adhere to all company policies, procedures and business ethics codes including anti-bribery policy and Environmental and Quality Management System (compliant with ISO 9001 and 14001). PERSON SPECIFICATION Required skills and experience ERP Systems Expertise: In-depth knowledge and understanding of Dynamics more »

and across other functions. Uphold company mission and values through accountability, innovation, integrity, quality, and teamwork. Support and comply with the company's Quality Management System policies and procedures. Maintain regular and reliable attendance. Ability to act with an inclusion mindset and model these behaviors for the organization. Ability to 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 »

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 »

and working with suppliers to arrange processing and shipment of critical devices. There will be some involvement with supporting other areas of the Quality management System as outlined in the Key responsibilities below. Key Responsibilities Ensure compliance with ISO 9001 Quality, ISO 14001 Environmental, and ISO 45001 Health and Safety more »

or a related field. - Proven experience in a Quality Systems role within the electronics industry. - Strong knowledge of ISO 9001 and experience with quality management system audits. - Excellent analytical skills and a methodical approach to problem-solving. - Effective communication skills, with the ability to engage stakeholders at all levels. Apply more »

systems and assurance, with relevant QHSSE experience in a manufacturing and/or project environment. Experience in the implementation and maintenance of a Quality Management System/ISO certification is essential. You are well organised, with good analytical and critical thinking skills, and excellent verbal and written communication skills. You 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 »

to completion of a satisfactory cleanout. Approving all documents including master Process Record Sheets (PRS's), monographs and procedures. Using Master Control electronic quality management system for document/deviation approvals etc and SAP for batch management/release. Complying with all environmental, health and safety requirements. Embodying our company more »

and guidelines including, but not limited to, Code of Business Conduct and Ethics, GDPR, and HIPAA. Support and comply with the company's Quality Management System policies and procedures. Regular and reliable attendance. Ability to work normal schedule of Monday through Friday during normal business hours. Ability to work in more »

and Flow Cytometry section. 2. To help support managerial responsibility for all coagulation analytical platforms and associated assays. 3. To help deliver and maintain QMS to comply with UKAS (ISO15189) standards in the specialist area. 3. To help ensure HR policies and procedures are effectively managed within Blood Sciences-Haematology. more »

prevent occurrence. Reduction in Quality Management System (QMS) non-conformances, and Customer Complaints & repeat process NC's. Timely implementation of product, process, and Quality Management System changes. Avoidance of product recalls. Compliance with approved procedures. Adherence to the QMS, GxP & Regulatory requirements. Develop, generate, and maintain documentation to support an … effective and compliant QMS, including: Product Routers & Assemblies (PRA), Material (DRM) and Product Specifications Product and Process FMEAs/Risk Assessments Customer Complaints Medical Device Risk Management Reports and Files Quality Inspection Procedures and Control Plans Quality Systems and Process SOPs and Work Instructions (PWI). Conduct internal Audits, GMP more »

for Daily Management of the Functional team and their performance; Leads people using company values and core behaviors with a GEMBA presence. Maintain Quality Management System in accordance with Corporate, BU and regulatory requirements advocating complainant change management. Leads and implement strategic initiatives to reduce the number of internal and more »

to deliver our service commitments. Highlighting any non-conformances to the relevant personnel. Supporting the QA team to include all parts of the Quality Management System that is in place to ensure we continue to develop activities and policies aimed at improving the effectiveness and efficiency of the service. The more »

range of responsibilities and duties with this role, as the Quality Assurance Engineer will be responsible for managing the EN9100 internal audits, maintaining the QMS, supporting continuous improvement and evaluating risk. The Quality Assurance Engineer will also be responsible for completing CAPAs with the audit team and participants. They will more »

levels of GMP, food safety and integrity standards. Responsibilities Include: • Supporting the overall technical strategy, tactics, policy & plans • Responsible for the company’s quality management system to ensure compliance with standards and (HACCP) procedures on food handling • Coordinate all quality assessment and laboratory activities • Ensure that both inbound and outbound more »

and completing corrective actions required to address any areas of poor performance, including, where required, staff performance management. Ensure all documentation required for Quality Management System is recorded and maintained Communicate efficiently, courteously and with clarity at all times, whether face to face, telephone or electronic methods referring enquiries to more »

as performance management, absence management, measuring results and how to have regular conversations. Adherence to Company policy and working to the company ISO Quality Management system (9001 certification) and company security management system (27001 certification in the UK) at all times. Work with the wider global HR team to ensure more »

manufacturing engineering, or similar. Experience in process and product validation (sterile packaging according to ISO 11607 would be advantageous). Understanding of a quality management system (ISO13485/FDA) and medical device manufacturing advantageous. Very good MS-Office skills, especially Excel. Strong organizational skills with the ability to communicate at more »

Work with the wider team to develop business processes, remove waste and non-value add activities 5. Ensure full compliance with the Companys Quality Management System 6. Pro-actively assist the Document Quality Team with creation of Documentation Packs for designated projects Experience/Skills: Qualified to HNC level minimum more »

hoc tasks, as required. Uphold company mission and values through accountability, innovation, integrity, quality, and teamwork. Support and comply with the company's Quality Management System policies and procedures. Skills Ability to manage multiple simultaneous tasks and meet deadlines. Ability to prioritize with drive to achieve results with a high more »

Computerized Systems Validation and knowledge of ISPE's GAMP and FDA 21CFR Part 11 would be advantageous. Adherence to SOPs and experience with a QMS will be required. The ideal candidate will have a life-science degree or similar with good communication, planning and organizational skills and be a strong more »