1 to 25 of 39 Permanent QMS Jobs in the Midlands

control of quality documents (SOPs, WIs, records etc) Management Representative responsible for ISO 14385 certification and maintaining the effectiveness of the Full Support Healthcare QMS Maintenance and communication where required of technical documentation Investigate and report on non-conformances, customer complaints and CAPA issues within specified timeframes Validation of sterilisation … deadlines. Must be adaptable, numerate, literate and be willing and quick to learn with the desire to succeed Knowledge and practical experience of using QMS software (Q-Pulse desirable).Job Offer Highly negotiable basic salary. Other benefits. Please contact Natalie Hudson at Michael Page Birmingham more »

safety legislation and standards. • Develop and monitor Leading & Lagging KPIs in collaboration with the Site Management Team. • Provide support for food safety and quality management system auditing at selected third-party pack sites. • Act as the Site Lead on Pest Management. • Actively support site hygiene management systems, ensuring effective chemical more »

Ideally a qualified, certified Project Manager. Overview: Own ISO 9001 Plan Responsibilities, Policies, and Objectives of the Project Your Project Documentation to Launch Quality Management System Performance for Certification Improvement activities Key Responsibilities – Project Manager Quality Systems Health and Safety in the workplace above everything else, leading by example and more »

of RCA tools such as 8D, 5WHY, ISHIKAWA, FMEA’s Champion and support the team of procedures, working instructions and SOP’s Maintaining ISO9001 QMS and implementing TQM Monitor output, quality & scrap rates. Improving OTD performance Maintain records of products and approved suppliers Continually improve QMS processes If you are more »

of all quality related subjects to the workforce Ensuring requirements of the company Quality Policy and quality objectives are met Reporting performance of the QMS and any needs or opportunities for improvements Reporting and investigating any instances of non-conformance Integrating customer standards into the QMS as required Development, issue more »

required by the organisation. Maintain and continuously improve the standard of Quality Assurance Support the maintenance and ongoing improvement of the Quality Management System (QMS) through internal audit and quality process creation. Create and submit FAIRs as per AS9102. Support the creation and submission of PPAP/DVI – PFC, PFMEA … Control plans, MSA, FAIR, capabilities studies, etc. Perform internal audits as per internal, customer and QMs criteria's. Promote and support the drive of continuous improvement in all quality processes. I'm keen to speak to Quality Engineer's with the following skillset: Experienced in either ISO 9001 or AS9100 more »

of RCA tools such as 8D, 5WHY, ISHIKAWA, FMEA's Champion and support the team of procedures, working instructions and SOP's Maintaining ISO9001 QMS and implementing TQM Monitor output, quality & scrap rates. Improving OTD performance Maintain records of products and approved suppliers Continually improve QMS processes If you are more »

Estimating Engineer E&I Location: This role is based in our Grimsby Office with an element of flexibility for remote working. Salary: Negotiable, depending on experience Company Benefits: 25 days holiday + bank holidays, death in service benefit, critical illness more »

milestone progress to the Project Lead, Programme Manager and Stakeholders. Maintain best practices within the Software Team, ensuring technical journals, essential research and company QMS process are followed. Leadership and administration of the Sprint process for the Software Team. Support the delivery of product firmware and software within the Software more »

milestone progress to the Project Lead, Programme Manager and Stakeholders. Maintain best practices within the Software Team, ensuring technical journals, essential research and company QMS process are followed. Leadership and administration of the Sprint process for the Software Team. Support the delivery of product firmware and software within the Software 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 »

below opportunity to join our innovative and conscientious team: Quality Systems Engineer Overall purpose of the role Responsible for driving the Quality Management System (QMS), aligning procedures and processes with rest of operations team to support the QMS. Lead and undertake … audits across all areas of the business. Provide training and champion the Quality Management System. Key responsibilities Support the effective implementation of the Quality Management System throughout the site, including any business accreditations. Maintain (and develop) the Quality Manuals and Quality Procedures and ensure contents are appropriate for business. Support … process and prevent occurrence of any non-conformity relating to product, process or system. Support develop and roll-out of activities that support the QMS and quality improvements, i.e. first off sample approvals. Support and lead process improvement activities. Write reports and present progress to Senior Management. Skills & Attributes Lead 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 »

Lead to join our Quality Team based in Coventry. Duties & Responsibilities As a Quality & Improvement Lead you will: Develop a project level QMS (Quality Management System), in line with the business QMS, specific to customer needs and provide process owners with support to devise and establish sector quality procedures, standards 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 »

in an engineering and/or manufacturing environment. Conversant with the process of attaining and maintaining accreditations to ISO 9001 and ISO 45001 Experienced QMS/H&S auditor This is a great opportunity to join a fast growing SME organisation and be a key member of their Senior Management more »

and encourage learning and development. As the Quality Assurance officer you will support the QA Manager in overseeing GMP compliance, contribute to the management of QMS and ensure the maintenance of quality certifications and standards throughout the manufacturing … testing and release of the product. Salary: £25-35k (dependent on relevant work experience) Key responsibilities: · Assist in maintaining the Company’s Quality Management system – including drafting of new procedures to enhance the companies QMS. · Support with assessment of deviation event investigations. · Support closure to plan of Change Controls more »

audits, and continuous improvement activities, upholding the standards for quality both within the company and suppliers by ensuring compliance to procedures within the quality management system and to manufacturing specifications. You will facilitate customers and supplier quality assurance activities including root cause analysis and quality improvement. Main responsibilities: Maintain and … enhance the Quality Management System (QMS) to ensure compliance with ISO 9001, AS9100, ISO 13485, and other relevant standards. Facilitate, control, and conduct internal audits to ensure continuous compliance and improvement. Assist in managing and hosting customer audits, presenting our processes and ensuring transparency. Act as a primary quality contact … AS9100, ISO 13485, IPC610 & IPC620 desired but not essential) Strong skills in customer interaction and managing customer-facing quality issues. Proficiency in using QMS systems and various quality resolution tools. Excellent report writing skills and the ability to use quality-related tools effectively. Proven track record in problem resolution and more »

eg GC, KF, UV-Vis, FT-IR. The use of a Chromatography Data System such as Empower in a regulated laboratory. Significant experience leading QMS driven aspects of a cGMP laboratory, Laboratory error investigation, OOS investigation, Deviation investigation and CAPA. Experience scheduling and planning workloads, resource and equipment including developing more »

the department. Develop process improvements within the ISO 27001 framework to mitigate risks. Ensure commissioning activities comply with project timelines and quality management standards (QMS). Support and Communication: Communicate directly with customers to resolve problems. Assist with fault finding and analysis on live systems in a remote support capacity. more »

and assist production team with machinery assembly, to include working overtime as and when required. · Actively support continuous improvement. · Adherence to ISO 9001 Quality Management System compliance. · Be prepared to learn a diverse set of products from differing brands and continually improve your product knowledge. Required Skills: · Experience in a more »

a medical manufacturer, offering progression, additional training, healthcare benefits, and more. THE ROLE: * Quality document Controller * Assist Quality Manager * Ensure Guidelines are followed * Maintain QMS * Mon-Fri 9am-5pm THE PERSON: * Document Controller with Quality background * Knowledge of ALCOA * Audit skills * Commutable to Worcester Reference Number: BBBH13645 Key Words: Medical … ALCOA, Devise, Quality, Assurance, QMS, Management, Audit, Document Controller, Worcester, Droitwich Spa, Bromsgrove, Stourport-on-Severn, Kidderminster, Great Malvern If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV. We are an equal opportunities employer and welcome applications from all more »

Auditing and measurement of CCP - Testing of equipment - Sample collection - Conducting hygiene audits and reporting findings to arrange any corrective action - Update the Quality Management System - Assessment of raw materials and finished products against relevant specifications Experience: - Previous experience in a quality assurance role, preferably in a manufacturing or food more »

Manufacturing support to the production areas with reference to quality issues Ensuring procedures are implemented or updated where appropriate. Actively support the business with QMS to ISO 9001:2015 certification Key skills and experience for the Quality Engineer job are: Previous work experience as a Quality Engineer or similar role 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 »