201 to 225 of 279 QMS Jobs

Negotiate schedule, risk, product features and resource trade-offs with project and program teams. Ensure all work product from the team meets Spacelabs processes, QMS requirements and follows best engineering practice, leading by example Ensure contract resources are effectively managed and deliver services and products as promised, and that meet … our QMS requirements. Generation of detailed project planning and process documentation Provide frequent communications and formal project reviews with senior management, program team and others as required. Qualifications: Experience in related industry and positions –capital equipment, medical device, or other regulated industry. Experience within a technical engineering role with a more »

Senior Buyer (Manufacturing) Location : Oxfordshire Job Type: Full time Contract Type: Permanent Salary: Competitive Benefits: Private healthcare, pension, income protection, life assurance, 27 days holiday + bank holidays, equity scheme Are you an experienced Senior Buyer of electronic components & electro more »

have a great opportunity to join our team here at The Cornwall Bakery in Callington, you will be responsible to execute the site Quality Management System audits according to the risk assessed schedule. Provision of detailed reports and escalation and verification of closure of non-conformances raised. You will need … to ensure that all aspects of the business are audited at the correct frequency to maintain food safety and quality. Ensure that the Quality Management System internal audit schedule is completed, and all actions closed out in a timely manner. Ensure GMP & QA CCP audits are conducted to schedule and more »

Job summary The Manchester University NHS Foundation Trust includes major teaching hospitals. A wide range of equipment is used for medical work - diagnosis, monitoring, therapy and technical work - throughout its wards, theatres, andclinical departments. The Clinical Engineering Department deliver high more »

ensuring timely and accurate responses. Contribute to the supplier qualification processes, including conducting supplier audits and assessments to evaluate supplier capabilities. Maintenance of the QMS: Contribute to the creation, maintenance, and organisation of quality-related documentation , including SOPs, work instructions, quality manuals, records and training material. Establish key performance indicators … Experience Degree in a relevant area of studies. 2 - 3 years’ experience in the role out of Quality policies. Knowledge of Quality Management Systems (QMS). Proven Auditing Skills. Continuous Improvement Mindset. Excellent interpersonal, verbal, and written communication skills. Experience of working at the headquarters of an international company. Fluent more »

avoidable issues. Engage with customers to understand their weighing goals and advise on best-fit solutions. Adhere with the Company’s Quality Management System (QMS) to safeguard the quality, consistency, and reliability of our services. Care and manual handling of weights and weighing equipment. Proactively communicate timely details of appointments more »

Job Summary QA Specialist is responsible for ensuring continued compliance of the Quality Management System of the company with the relevant Medical Device Directives, Medical Device Regulations, International Standards, and Customer Requirements and that this is maintained and implemented accordingly. Responsibilities Provide day-to-day support and be responsible to … maintain the effectiveness of the Quality Management System, including, but not limited to, Document Control, CAPA, Vigilance, Risk Management, Internal Audit, Post-Market Surveillance, Supplier Monitoring and Assessment and Product Release activities Contribute to strategic improvement projects to improve business processes in line with the applicable regulatory requirements and Medicareplus … times To show initiative in problem solving by identifying and recommending solutions to problems encountered To maintain a personal knowledge of the current Quality Management System and Regulatory Requirements Please note that the duties and responsibilities within this role may change over the course of employment, which will require flexibility. more »

compliance with ISO 13485, UK MDR 2002, MDR 2017/745, MDD 93/42/EEC, MDSAP, and other regulations. Prepare and maintain QMS and regulatory documentation. Assist QA Admin team with product approvals for UK and international markets. Evaluate suppliers and conduct approval audits. Document quality audits to … in a production/manufacturing environment. Internal and external quality auditing experience to ISO 13485. Passion for quality excellence. Previous quality assurance experience, including QMS documentation. Knowledge of CAPA and root cause analysis tools. Practical problem-solving approach. Understanding of ISO 14971 quality risk management principles. Self-motivated and team more »

and knowledge. Manage HSE policy and system framework in coordination with Group Health and Safety and client EHS representatives. Oversee the Quality Management System (QMS) in line with contract and scope of QMS requirements. Ideal Candidate: Location: Based in either UK, Ireland, Spain, Belgium, Switzerland, or Netherlands. Experience: Solid background more »

required corrective actions Ensure products and ingredients are evaluated against specification Support the promotion of a quality culture and help to develop the quality management system Coordinate QA requirements for product launches e.g. update of required documentation/systems, liaison with Process team/line support to ensure product is … manufactured to correct standard Plan and co-ordinate work of the QA team to meet requirements of the quality management system and the needs of the business About you. Ideally you will have a good practical working knowledge of food safety legislation and quality requirements. A strong QA background is more »

Job summary We have an exciting opportunity for an enthusiastic and motivated person to lead our mechanical engineering team in Radiotherapy Technology Services (RTS) at Bexley Wing, St. James's Hospital, Leeds . Working collaboratively with clinical and scientific staff more »

Job summary Are you looking for an exciting new challenge in a place to take your career to the next level? Would you like to join a friendly, progressive, innovative team and play a part in the transformation of pathology more »

and administration of the Quality Management System (QMS). As Document Controller , your important role will include: Managing documentation control processes within the Quality Management System Coordinating documentation change requests Formatting and reviewing documentation Ensuring reports are distributed from the Quality Management System Supporting departments with requests for documentation For more »

conformance reports (NCRs). Final review of all fabrication and assembly documentation. Collate and update SQEP files. Conduct audits on the Quality Management System (QMS). Requirements: CSWIP 3.1 certified is essential. Experience within Nuclear or MOD highly advantageous. Experience with Life-Time Quality Records (LTQRs) Pay Rate: circa more »

laboratory tests with the production team. Implement suitable product and process changes to satisfy Customer Specific Requirements and that of the Quality Management System (QMS). Perform Root-Cause Analysis with process and test data to implement sustainable corrective actions. Understand risk management and the process-based approach to quality more »

The Quality Manager will be a key member of the SYBP Quality, Risk and Governance Team, responsible for ensuring that the Laboratory's Quality Management System functions correctly. The Quality Manager is accountable for: Ensuring the laboratory Quality Management System is designed, implemented and maintained becoming progressively more effective and … relationships with a wide range of stakeholders in order to engage with them. Experience of training and assessing staff competencies relating to the Quality Management System functions e.g. Audit, Non-Conformances, Document Control etc. Experience in administration, managing and review/approval of electronic errors and incidence records e.g. Datix more »

and spoken Ability to interact at all levels Customer facing experience AS9100, BSEN ISO9001 experience Are you familiar with ISO 9001:2015 and AS9100 QMS standard … requirements? As the Quality Assurance Supervisor for the companys Avonmouth operation, you will be required to flow down the requirements of the company Quality Management System & AS9120 to site employees and advise on any relating queries. This is a new role for the company where you will: Monitor and measure more »

completed on time. Support the Quality Manager as required. Training production staff in in-process control and coaching staff in BMRs. Promotion of the QMS through coaching staff in the correct use of SOPs, documentation and working practices. Support staff during investigations through the use of problem-solving techniques. Support … with our audit plan. Gather data for the preparation of quality metrics . Provide QA support to all departments to ensure compliance with our QMS, customer and Regulatory requirements. Assist in the management of change through the correct use of change controls, information and training. Skills & Experience Required: Interpersonal skills more »

Quality Management System Lead Permanent Reading MBNL is owned equally by EE and Three, two of the UK’s most recognisable and innovative mobile operators. They are our shareholders, but to us they are also our customers. Continuing to manage, maintain and enhance the best network in the UK, and … relevant standards, specifically ISO9001 and ISO45001. What you will do: responsible for the implementation and ongoing management of an integrated health, safety and quality management system aligned to ISO45001:2018 and ISO9001:2015 requirements, potentially widening to other management system standards over time (e.g. ISO14001:2018, the creation and delivery … metrics and KPIs required by MBNL. as the primary point of contact with external bodies with responsibility for management system certification. The successful Quality Management System Lead will have: knowledge of quality, health, safety, and environmental management systems of developing and implementing quality, health, safety, and environmental systems. knowledge of more »

The role of the QA TL (Compliance) is to ensure governance and compliance of the Pharmaceutical Quality Management System (PQS) and maintain Regulatory Registrations/Licenses/Certifications at Piramal Grangemouth. The position holder will have responsibility to coordinate, maintain and promote compliance, leading continuous improvement of quality and regulatory … implementation of risk mitigation plans. Working with the wider site functions to drive down out of compliance events, identify and implement quality improvements Coordinate QMS training for site employees and ensure this adheres to current regulatory requirements Maintain responsibility as the site system owner for the Trackwise electronic QMS Support more »

grade AA* facility. Overview: To ensure that all the products produced are assessed in accordance with the companys and customers requirements, the site Quality Management System and HACCP System, in order that the quality, safety and legality can be assured and that all the necessary information is accurately recorded and … all members of staff in food hygiene, health & safety, manual handling, fire safety, chemical safety, and allergen awareness training. To assist in writing site QMS in accordance with BRC policies and procedures. To support the Technical and broader factory team during customer and compliance officer visits. To work as an more »

reviews with each Account Manager. Offer suggestions for continuous improvement to project management software and procedures. Report to Management on the performance of the QMS; on opportunities for improvement; on change requirements; on innovations Ensure the promotion of customer focus Ensure the integrity of the QMS is maintained - Comply with more »

Role Overview : We are seeking a highly motivated and skilled Electronic Design Engineer to join our dynamic team in Bristol. The successful candidate will be responsible for the design, development, and validation of electronic systems and subsystems for our advanced more »

Position : Production Engineer Sector : Manufacturing/Engineering Location : Sheffield Salary : £43,000 Shifts : Days/Early finish on Friday The Production Engineer will be responsible for providing front line support for all manufacturing processes. This will be inclusive of CNC more »

Are you a Test & Commissioning Engineer looking for a new challenge? Do you have a background in manufacturing and production? We are looking for a Test & Commissioning Engineer to join our growing CMS2 team in Portsmouth. This is a fantastic more »