1 to 25 of 85 QMS Jobs in the UK excluding London

for quality management, quality assurance, and quality auditing tasks related to pharmaceutical products. Ensuring products are fit for purpose before release for use or commercial sale. Maintaining and improving QMS' performance by ensuring items such as deviations, CAPA and change control for which you are the owner are progressed in a compliant and timely manner and all other items are … a timely manner in line with company procedures. Participate and/or host internal and external audits inclusive of customer and regulatory audits. Competent to author and approve routine QMS activities. Performing Root Cause Analysis using problem solving tools such as Fishbone, 5 Whys etc. Authors, reviews, and approves Controlled Documents in accordance with procedures. Will support in delivering the … site GMP training as required. Will conduct the internal audit programme. Will support the maintenance of the site QMS and facilitate reporting of relevant KPIs within department and across site as required. Ensure customer or supplier complaints are satisfactorily investigated and communicated. The Person:- The ideal Candidate will hold a degree in a STEM related subject Experienced in batch review More ❯

At Kindeva we make products that save lives, ensuring better health and well-being for patients around the world. Role Overview: This role is joining our dynamic team in Manufacturing Technology (Process & Manufacturing Engineering) where you will be supporting the More ❯

matters. Assist with third-party and customer audits, including the implementation of corrective actions. Manage the internal audit programme, perform internal audits, and oversee corrective actions. Maintain the Quality Management System, including inspection and test data and quality records. Support resolution of customer complaints in collaboration with the Quality team. Create and maintain Quality Plans to ensure compliance with contract … technical drawings and specifications. Familiarity with Geometric Dimensioning & Tolerancing is a plus. Good understanding of manufacturing processes and quality control systems. Required Experience: Working knowledge of ISO 9001 Quality Management System standards and practices. Familiarity with mechanical inspection equipment; experience with CMM or FARO arm is a plus. Experience managing calibration systems and document control. Competence in developing and applying More ❯

a key role within the Quality team, reporting to the Quality Manager and responsible for leading a team of QA professionals while maintaining and developing the site's Quality Management System in line with customer, legal, and audit requirements. Key Responsibilities: Oversee and improve the Quality Management System, ensuring compliance with customer and legal standards Lead investigations into complaints and … improvement initiatives What We're Looking For: Degree in a food-related discipline or minimum 5 years' QA experience within FMCG Strong knowledge of BRC standards, internal auditing, and QMS implementation Proficient in Microsoft Office, with strong attention to detail and reporting skills Experience in team leadership or coaching is desirable Previous involvement in third-party or customer audits is More ❯

third party surveillance and customer audits, including corrective actions that arise. Manage the internal audit programme, perform internal audits and manage corrective actions that arise. Maintenance of the Quality Management System, including maintaining inspection and test data across local Quality system records. Assist the Quality Director and Quality Manager in resolving customer complaints. Produce Quality Plans to ensure compliance with … others. Ability to read technical drawings and specifications. Geometrical Dimensioning & Tolerancing knowledge is an advantage. Thorough knowledge of fundamental manufacturing processes and control systems. Experience required in: ISO9001 Quality Management System requirements and maintaining a QMS. Mechanical measuring and inspection equipment. CMM or FARO arm experience would be an advantage. Calibration systems and control. Documentation systems and control. Raising and More ❯

all key process personnel are appropriately trained prior to implementation of a new Computerised System procedure. Drive post-implementation reviews and continuous improvement of computerised systems. To support the QMS as a subject matter expert on Computer systems used to store and process pharmaceutical data. Maintain compliance and audit readiness for all electronic systems and documentation . Support the reporting … installations and version upgrades Data migration and system archiving Management of audit trails, user access, and data integrity in Empower Demonstrable success in leading system migrations or large-scale QMS digitalisation projects. Experience in writing and maintaining validation documentation in line with GAMP 5. Good working knowledge of Computer System Validation. Familiar with electronic quality management systems (eQMS). Familiar More ❯

This approach is fully embraced 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 obligations to act responsibly, ethically More ❯

Job Title: Senior QA Specialist Salary: £38,000 - £45,000 Location: Greater Manchester SRG is currently working exclusively with a highly successful & award winning, CDMO based in Greater Manchester. Growing rapidly, the business specialises in taking products from discovery, all More ❯

for purpose management system is in place covering, quality, safety, security, health and environmental issues. Facilitate the implementation of the QSSHE management system. Support the maintenance of the Quality Management System utilised within the office. Provide leadership to the SNS organisation on quality issues. Support SNS QSSHE Team in the delivery of day-to-day activities such as Total Risk More ❯

will support the Head of Quality to lead and coordinate the Quality function across the business, with a primary focus on developing, maintaining, and enhancing our Quality Management System (QMS). You will play a key leadership role in driving Quality Improvement initiatives, building and leading a team of Quality Engineers, ensuring effective regulatory compliance and risk management. Lead the … QMS team, focusing on investigation simplification, robust root cause analysis, and effective CAPAs. Deliver training on investigation techniques, root cause analysis, and CAPA effectiveness. Generate and maintain the site Risk Register and ensure visibility of key risks across stakeholders. Drive continuous Quality Improvement across all UK sites. Lead Quality Improvement initiatives and the generation of key quality metrics. Facilitate and … participate in the Quality Committee. Ensure compliance with current regulatory requirements (e.g., MHRA, HTA, FDA). Support and deputise for the Head of Quality when required. Regularly report on QMS performance and risk-based deficiencies. Ensure quality systems are in place for document control, investigations, and change control. Recruit, coach, and motivate Quality staff to maintain high performance and capability. More ❯

for a Quality Assurance Manager to join an industry leading baker of a variety of delicious treats and cakes. You will be accountable for the implementation of the Quality Management system site policies and procedures. Driving for compliance to site standards and continuous improvement of food safety/product quality/legality and food safety culture. Key accountabilities as Quality More ❯

requirements for Quality activities. Stay up to date with the latest advancements in Quality management technologies, methodologies and best practices. Qualifications & Requirements - Quality Systems Engineer Minimum 3 years Quality Management System experience in a complex ISO9001/AS9100 certified manufacturing environment. Skilled in documentation management and configuration control Proficient auditor of management systems and processes Experienced in the use of More ❯

requirements for Quality activities. Stay up to date with the latest advancements in Quality management technologies, methodologies and best practices. Qualifications & Requirements - Quality Systems Engineer Minimum 3 years Quality Management System experience in a complex ISO9001/AS9100 certified manufacturing environment. Skilled in documentation management and configuration control Proficient auditor of management systems and processes Experienced in the use of More ❯

that arise; communicate and escalate as required Deliver the quality message around site through team training, presentations and tool box talks Support the monitoring and compliance of the Quality Management System as it applies to site Operations Plan, conduct and review inspections for all areas as per the inspection plan. Communicate findings and work with areas leads to implement corrective More ❯

This approach is fully embraced 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 obligations to act responsibly, ethically More ❯

appropriate. Pro-actively ensure that Digital changes are delivered to best practice with respect to organisational, NHS and legislative requirements and guidelines including information governance and security. Implementing quality management system, undertaking audits designed to improve IT systems and services. Ensure there is a proactive and comprehensive approach to risk management and be responsible for service continuity for own area More ❯

experience with deep understanding of GxP regulations, FDA 21 CFR Part 11 compliance, and validation methodologies •? Design and develop complex integration flows connecting S/4HANA with LIMS, MES, QMS, and regulatory reporting systems using REST, SOAP, OData, IDoc, RFC protocols •? Lead and mentor team of 6-10 integration developers while collaborating with functional consultants and business stakeholders •? Ensure regulatory More ❯

root cause analysis investigations for internal non-conformances. Support continuous improvement teams for quality improvement and waste reduction. Support the QC manager in ensuring standards defined within the quality management system are maintained and reflect the correct standards to match customer expectation. To highlight inconsistencies and errors within QC documentation and processes Ensure these are recorded in an appropriate manner More ❯

We are seeking a Quality Assurance Specialist to join a leading pharmaceutica logistics company. This role focuses on supporting the implementation and maintenance of the Quality Management System (QMS) in line with ISO 9001 and ISO 13485 standards, and ensuring compliance with EU GDP guidelines. Key Responsibilities: Maintaining and enhancing the QMS to meet regulatory, ISO, and client requirements. Supporting More ❯

We are seeking a Quality Assurance Specialist to join a leading pharmaceutica logistics company. This role focuses on supporting the implementation and maintenance of the Quality Management System (QMS) in line with ISO 9001 and ISO 13485 standards, and ensuring compliance with EU GDP guidelines. Key Responsibilities: Maintaining and enhancing the QMS to meet regulatory, ISO, and client requirements. Supporting More ❯

Regulatory Affairs Specialist to join their QA/RA team on a 12-month maternity cover contract. Key Responsibilities: Lead and support continuous improvements within the Quality Management System (QMS) Collaborate with all departments and external stakeholders to maintain regulatory compliance Provide QA/RA expertise throughout product development and change control processes Guide risk management and post-market surveillance … Review SOPs, software development documents, and regulatory submissions Deliver training to ensure quality and regulatory understanding across the business Perform internal and supplier audits and support external inspections Validate QMS-related software and manage eQMS platforms Assist in compiling and maintaining technical and regulatory documentation Benefits At Genedrive, youll be part of a passionate and expert team, making a tangible More ❯

quality system to ISO 13485 standards and associated product certification. As a Quality Systems Engineer, you will: Support the maintenance and continuous improvement of our ISO 13485 compliant Quality Management System with activities including document control, training management and change management. Draft and update procedures, work instructions, and quality documentation. Collaborate closely with Engineering (Software and Hardware) and Customer Support More ❯

consider 4 days/week and partially remote arrangements for the right candidate. Key Responsibilities - Lead the quality and compliance functions of the organization - Manage and own the quality management system - Support development of organizational strategies by aligning quality and compliance with company goals - Sign off on deliverables as per the approval matrix - Support and guide the team in ongoing More ❯

to identify areas for reliability and quality improvement; initiating and facilitating actions to implement improvements effectively using problem-solving techniques (8D, 5Why, etc.). Responsibility for the maintenance of QMS, ensuring compliance with all regulatory requirements and standards adopted by the company. Formulate, develop, and promote policies, processes, procedures, objectives, and measures for the continued operation of QMS (e.g., Quality … instructions for company processes and procedures. Organise and conduct internal and external audits to ensure adherence to regulations and standards. Collate and deliver performance data as part of the QMS review to senior management. Identify training needs and implement company-wide compliance training. Train and coach staff regarding quality and environment functions. Establish quality contracts with customers and suppliers. Act More ❯

progress, co-ordination and feedback Responsible for the production, review and monitoring of construction methodology documentation including RAMS and ITP's to ensuring compliance with the company's quality management system and the employers requirements. Responsible for production of as-built documentation from site. Responsible for materials forecast, procurement and reconciliation. Help collate and site data for inclusion in Daily More ❯