1 to 25 of 242 QMS Jobs in the UK

in line with the QP/ITP schedule and are issued for inclusion in the LTR concurrent to the works completed. Undertake periodic Quality Management System audits both internal and external to ensure that the system and procedures are adhered to. Monitor Vendor Performance and carry out Supplier/Subcontractor more »

bar to make up our datalogger tools. This process requires great attention to detail due to the fine tolerances involved. • Work to all Company QMS policies and procedures as per ISO 9001:2015. • Ensure that a safe working environment is maintained at all times through compliance with Health and safety more »

will be leading the validation function to be able to execute report activities within the framework of GMP - Annex 11 & 15 in compliance with QMS requirements. In addition, they will be supporting multiple validation projects, liaising with the project departments and the associated departments to ensure work is completed in more »

the site Ensure that the HACCP (HACCP/TACCP VACCP) program is maintained and aligned with best practice at all times Ensure that the QMS is effectively implemented and amended to ensure product standards are maintained Ensure the QA and Hygiene teams are run effectively and adequate technical resources are 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 »

the customer portal & specification systems. Working with the Process Lead and the wider business. Attending customer pre-artwork meetings Help support with the sites QMS and Internal audit process by conducting internal audits. Maintain nutritional trackers Advise the site team of any key update on legislation/customer requirements About more »

lab analysis Working closely with other sites for product specifications and documentation. Dealing with external stakeholders for food safety, quality and importing Maintenance of QMS Experience & Skills Required: The business is looking for an individual who has experience within the food industry. You must be able to lead, motivate and more »

in upholding the highest standards of quality! For this role,you must be willing to obtain CTC clearance Key Duties • Active promotion of Quality Management system awareness. • Review and update site quality plan • Produce and review Inspection and Test Plans and monitor compliance • Production of Work Packs • Weld Inspection (only more »

job description carefully before applying, thank you) Primary Objectives: The Quality Assurance Associate is responsible for helping to maintain and improve the DnaNudge Quality Management System as part of the Quality team by identifying potential improvements and efficiencies and helping to develop, revise and implement Quality procedures and policies. The … compliance of all regulatory requirements. Participate in the execution and support of internal and external regulatory audits and inspections. Support the maintenance of DnaNudge QMS program ensuring all processes are compliant to the relevant standards. · Manage some DnaNudge documentation associated with the QMS where required · Perform initial quality reviews of … internal auditor · (Desirable) Has worked in a similar role within the Medical Device/Pharmaceutical industry · (Desirable) Working knowledge and experience with a Quality Management System, such as deviations, investigations, CAPA, and customer complaints. · (Desirable) Experience of ISO certified QMS (ISO13485) Knowledge (Essential) In depth understanding of approaches to quality more »

United Living Group is a collection of four businesses dedicated to creating a connected, sustainable future: United Living Property Services: Revitalizing homes and communities through the regeneration of living spaces. United Living Infrastructure Services: Delivering resilient infrastructure for a stable more »

Atlas Endoscopy Atlas Endoscopy is a game-changing medical device company with the ambition to democratize colonoscopy and increase capacity in the healthcare system by bringing to market the most advanced robotic colonoscopy system. Atlas Endoscopy was founded by an more »

leading pipeline. • Serve as the development and technical contact for customer teams, leading product issue and crisis management efforts to minimise business impact. • Utilise QMS data to monitor and review performance, taking appropriate action for improvement. • Stay ahead of technological developments, optimising systems and processes for a more cost-effective 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 »

the management and scheduling of all GCP supplier and site audits. Ensure a current schedule is maintained for these activities. Provide input into the QMS and at the regular Quality Management Review Meetings on GCP activities and metrics. To chair these in the absence of the Head of Quality. Represent more »

molecular biology techniques Knowledge and experience of recombinant protein purification and analysis methods Strong time management and communication skills Experience in working under a QMS is desirable Knowledge and experience in enzyme biochemistry Experience in Microbiology/Fermentation Why Apply? Salary DOE, plus performance bonus and benefits package This company 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 »

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 »

collect information for the client handover pack to all company policies, procedures and business ethics codes including anti-bribery policy and Environmental and Quality Management System, compliant with ISO standards For more information please reach out to s.bishop@progressivege.com 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 »

hunt for a brand-new QSM Contractor to join the team on a hybrid, contract basis. The Role: Support the maintenance of the Quality Management System, act as Business Administrator for Veeva eQMS, oversee quality associated records and ensure these activities conform to regulatory requirements. Manage the controlled document scheme … system during regulatory and client audits/inspections. Management of the training matrix and Veeva Training to ensure fit for purpose. Provide support and QMS data for internal and external meetings, including the Quality/Metrics Strategic Working Group (SWG). Maintain reports and dashboards in Veeva. Provide eQMS training more »

is responsible for managing all internal and external Quality Management aspects of a contract/project, ensuring implementation, maintenance, and improvement of the Quality Management System throughout the Tender, Project implementation, and After Sales support. Benefits: Remuneration: Competitive salary, an excellent package and hybrid working Professional Development: Opportunities for growth … equivalent qualification. Minimum 2 years of experience in a Quality Assurance role. Minimum 2 years of experience in customer-facing roles. Proficiency in quality management system requirements such as ISO9001/TL9000 (QMS). Desirable skills include Project Management, Basic Commercial Skills, and/or Lead Auditor training. How to more »

point of contact for their laboratories engaged in exploratory analysis of patient samples. You will be responsible for: Implementation of the company's quality management system relevant to GCP, including laboratory analysis of clinical samples, external vendor oversight, and training on quality procedures Acting liaison and support for Immunomonitoring and … assisting in quality assurance aspects of the company's Clinical Trials Act as the system administrator for the eQMS, write and/or review QMS documents, including SOPs, deliver training to laboratory teams and eQMS users Plan and conduct of audits, including internal, vendors, clinical sites, and external laboratories Provide more »

work on a cutting-edge Battery Energy Storage System (BESS) project connecting to the national grid. Responsibilities: Develop and implement a Quality Management System (QMS) pack according to ISO 9001:2015 standards Oversee the achievement of technical standards on the ground Compile quality documentation including Quality Plans, Inspection Test Plans more »

for a Senior Clinical Quality Assurance Specialist to join a well established QA function. KEY RESPONSIBILITIES: Coordinating the implementation of the company's quality management system pertaining to Good Clinical Practice (GCP), including oversight of external vendors, training on quality procedures, and performance monitoring against established standards. Serving as the … and Clinical Plans. Writing and/or reviewing Quality Management System (QMS) documents, including SOPs. Acting as the system administrator for the electronic Quality Management System (eQMS) and managing documents within the system on a day-to-day basis. Generating and monitoring quality metrics, including those derived from the eQMS. … practices related to GCP and GCLP, with an understanding of considerations for Advanced Therapy Medicinal Products (ATMPs). Skilled in maintaining and monitoring a QMS, preferably in a small/start-up organization environment. Educational Requirements: Bachelor's Degree in Life Sciences, Pharmacy, or Regulatory. Understanding of immunology is desirable. more »

successes and ambitions to grow further. We are looking for someone who has ideally gained experience within a manufacturing environment and has knowledge of QMS and Supplier approval processes. THE ROLE: Management of all raw material and packaging supplier approval processes to ensure compliance with the Technical and Quality Assurance … new product launches by ensuring all supplier and raw material documentation is obtained prior to product trials Completing internal audits of site systems and QMS procedures. Member of the sites product defence team. THE PERSON: Previous experience in a Food manufacturing environment ideally. HND or Degree educated - in a technical … discipline. Knowledge of QMS & Supplier approval processes. Good understanding of food legislation. Great communication skills and a good attention to detail is paramount. BENEFITS: £28,000 + 25 days + Bank Holidays, Flexible working, Flexible working, Referral scheme, Sick pay Please contact Brandon Hewitt-Hunt for more opportunities in Engineering more »