15 of 15 QMS Jobs in the South East

Quality Management Representative, reporting to senior leadership and ensuring the ongoing effectiveness, compliance, and continuous improvement of the Quality Management System (QMS). They will provide expert guidance across product development, manufacturing, and operational teams to maintain compliance with applicable medical device regulations and quality standards. This hands-on leadership … stakeholders. Required Skills & Experience: Proven experience in Quality Assurance within the medical device industry. Strong knowledge of medical device design, development and Quality Management Systems (QMS). Working knowledge of ISO 13485, FDA 21 CFR Parts 820 & 11, and EU MDR (2017/745). Experience leading internal, external ...

roles in regulated manufacturing environments. Strong knowledge of global regulatory authorities including FDA, GMP, GCP and GLP requirements. Proven expertise in Quality Management Systems (QMS), with a particular focus on GMP compliance and data integrity. Demonstrated experience with regulatory inspections, audits, and quality assurance activities, including supplier quality management. ...

engineering highly desirable. * Min 5 years' experience in aerospace industry or equivalent at engineering, design & development, or quality positions. * Proficiency in ISO9001, AS9100 QMS standards deployment and implementation. * Previous experience working with EASA/CAA part 21J. * Experience in internal and external audit and auditing techniques, lead auditor trained preferred. ...

able to perform well in this role! Measuring and reporting dimensional matters on complex injection-moulded or metallic components as required by quality management system and client specifications In depth and extensive knowledge of GD&T and recognised drawing standards (ISO 1101, ASME Y 14.5, BS 8888) Methodical approach ...

into the new system, helping maintain compliance and supporting the successful delivery of the project. Responsibilities include: Supporting the implementation of a new Quality Management System Uploading, transferring and maintaining quality documentation Copying and migrating documents into the new platform Checking document accuracy, formatting and version control Ensuring records ...

facilities. Undertaking System Administration tasks identified within the System Team Backlog in accordance with the policies and procedures detailed in the Air QMS (Quality Management System). Monitoring and reporting on environment performance. Manage the environment in order to maintain its performance and availability. Ensuring that all data held … backed up and can be restored in the event of any data loss. Work within the boundaries of the AMPA Quality Management System (QMS) and the procedures defined within it i.e.; Starters & Leavers process. Internal equipment moves. Providing Licencing support as required: Obtain Licence quotes for software used ...

complex engineering and data platforms. Key Responsibilities Own the Core: Lead SAP-centered capabilities across ERP, S&OP, IT EAM, WMS (SAP-first), and QMS (SAP-first). Drive Integration: Define and architect seamless integrations between SAP and PLM, MES, and enterprise data platforms. Lifecycle Support: Actively support ...

improvement Requirements Previous Technical Product Owner or Senior Business Analyst experience Hands-on Veeva Vault RegulatoryOne experience Product Lifecycle Management (PLM) Quality Management Systems (QMS) Agile methodologies Computer System Validation (CSV) GxP/FDA regulated environment experience This is a fantastic opportunity to join a global transformation programme delivering innovative ...

Electrical/Electronic formal qualifications * Good IT Skills, experience with excel, word and data retention systems. * Experience of working in accordance with a Quality Management System * Ability to communicate effectively with customers and other members of the team. * Experience and knowledge in one or more electrical safety standards e.g. ...

quality requirements for their approval, marketing and lawful commercialization. The role will lead the implementation of ISO13485 and management of the related Quality Management System, the regulatory strategy across EU (IVDR), UK (UKCA/MHRA) and US (FDA, CLIA, LDT, SaMD) markets, and the regulatory and quality interfaces with biopharma … submissions, and embedding compliance across product, R&D, clinical and commercial teams. Responsibilities Key Responsibilities — Quality Own, maintain and continuously improve PrecisionLife ’s Quality Management System to EN ISO 13485:2016, US FDA QMSR (21 CFR 820 transition), CLIA and applicable LDT requirements. Act as Management Representative in accordance with ...

strong technical knowledge in relevant fields Familiarity with relevant safety procedures and regulations Able to understand the importance and principles of an advanced Quality Management System Experience in maintaining and repairing Machinery and Production equipment Experience with industrial networks and control systems Excellent analytical and critical thinking skills with …/HND/C&G or Degree in Engineering or related field Previous knowledge and understanding of the importance and relevance of a Quality Management System Experience of updating records of tasks/spare parts used from store and work completed, using the CMMS system Service Leavers and EX Forces ...

rigorous quality standards. Change Control Management: Provide expert guidance on validation changes and lead change control activities in accordance with established quality management system (QMS) procedures. General QA Support: Collaborate closely with the wider Quality Assurance team to support audits, risk assessments, and continuous improvement initiatives. What We Are Looking ...

excellent prospects for long-term career development. In this role, the successful Quality Assurance Officer or similar will maintain and improve the Quality Management System, review batch manufacturing documentation prior to release, manage CAPAs, Deviations, Change Controls and investigations, support internal and supplier audits, and work closely with Production … will also be opportunities to become involved in validation activities, supplier quality and wider continuous improvement projects. The Role: Maintaining and improving the Quality Management System within a GMP pharmaceutical manufacturing environment Reviewing batch records, quality documentation and managing CAPAs, Deviations and Change Controls Supporting audits, validation activities and continuous ...

growth biopharma innovators. Serve as a trusted advisor on digital manufacturing trends, GxP compliance, and operational excellence. Drive adoption of cloud-based MES and QMS, AI and Analytics platforms through value-based, consultative selling. Partner with solution engineering, marketing, and customer success teams to deliver compelling business cases … sciences, pharma manufacturing, or regulated industries. Deep understanding of CGT, CDMO, and biologics manufacturing workflows—from process development through commercial scale. Familiarity with MES, QMS, LIMS, and related digital manufacturing systems strongly preferred. Proven track record of closing multi-million-dollar SaaS or digital transformation deals involving long sales cycles ...

Master, facilitating ceremonies and promoting agile maturity across teams. Deliver quality controls and standards on projects in line with the organisations Quality Management System (QMS). Facilitate stakeholder management by developing and maintaining effective relationships with internal and external stakeholders. Monitor project performance using key metrics, analysing trends and providing ...