1 to 25 of 247 Permanent QMS Jobs

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 »

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 »

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 »

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 »

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 »

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 »

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 »

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 »

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 »

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 »

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 »

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 »

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 »

with strong quality orientation. 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 »

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 »

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 »

which utilise the databases provisioned. -Preparing and delivering regular reports in relation to database performance, trends, and improvements. -Ensuring all documentation complies with ISO9001 QMS and best practice. -Ensuring the team have the appropriate resource levels to deliver business outcomes. Required Experience -Degree in Computer Science, Information Technology, or a more »

SQL and either Python or R. 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 Significant experience of working in the data domain in technical roles more »

Ideally experienced in the Medical Technology Sector. A knowledge of important IT Standards & Methods (eg ISO27001, ISO 80002-2, ITIL) or ISO 13485:2016 QMS for Medical Devices. Your Profile: Completed relevant Scientific or Technical University Degree. Strong communication skills, assertive & highly quality-oriented. Fluent English & good German language skills more »

products at its two facilities in Spokane, Washington, and Hebron, Kentucky. PM22 We are currently seeking an experienced Quality Systems Coordinator to manage the QMS to ensure compliance with ISO 9001:2015 and AS 9100 standards. The ideal candidate will have an Associate of Arts degree in a relevant technical more »