1 to 25 of 31 QMS Jobs in the East of England

and SME for all compliance platforms, responsible for training users and leading continuous improvement efforts. Lead and represent in validation efforts, ensuring consistency with QMS and corporate policies. Qualifications Bachelor's or Master's degree in Occupational Health and Safety, Construction Management, Engineering, or a related field. Minimum of more »

team Facilitate project progress meetings with the project team Lead communications with suppliers and clients Contribute to sales activities, marketing materials and the Quality Management System as required What skills and knowledge can I bring? Experience managing the development of firmware for embedded products and systems (user interfaces, sensors, wireless more »

and SME for all compliance platforms, responsible for training users and leading continuous improvement efforts. Lead and represent in validation efforts, ensuring consistency with QMS and corporate policies. Qualifications Bachelor's or Master's degree in Occupational Health and Safety, Construction Management, Engineering, or a related field. Minimum of more »

burr components. - Running and checking “1st” off and random batch inspection. - Observe machine operation to verify accuracy of machine settings. Technical Understand the Quality Management System Quality Brief. Responsible for the production of Company products. Achieve production targets and deadlines. Work from engineering drawings. To clock in/out and more »

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 »

Hobson Prior is seeking a Quality Assurance Specialist on a permanent basis. This role focuses on maintaining and improving the Quality Management System (QMS) whilst developing diagnostic capabilities. This includes supporting internal audits, assisting with client audits, and providing support for quality department initiatives. Responsibilities: - Work alongside the team to … maintain all aspects of the QMS, including Change Controls, Non-Conformities, CAPAs, and Customer Complaints. - Support continuous improvements in the QMS and maintain compliance of Quality processes by conducting internal audits. - Assist with audits, both internally and externally, including desk-based, remote, and on-site audits of subcontractors and suppliers. more »

clinical study and FDA approval. Implement verification and validation test plans and protocols for the system/product, documenting all activities within the Quality Management System (eQMS). Contribute to the development of Work Instructions and Standard Operating Procedures (SOPs). Collaborate with the Engineering, Manufacturing and Biology teams working more »

lyophilisation and quality control and production of small-medium scale batches. Handling receipt of reagents and chemicals -including aliquoting, storage and uploading onto the QMS as necessary. Working alongside CMO’s and in-house specialists to support the production scaling activities. Create and implement QC and validation protocols, ensuring that more »

Main Duties (but not limited to): Completing technical checks in the factory (quality checks, carcase inspections, pH testing, steriliser checks etc) Reviewing and filing QMS paperwork from various production departments. Liasing with production teams in relation to paperwork completion, where necessary. Collating and registering all samples and results for microbiological more »

The British flower market is worth £1.2bn and MM Flowers supplies fresh cut flowers and bouquets to the U.K.s and Europes leading flower retailers. We grow and source the highest quality and most beautiful blooms across the world, delivering colour more »

ensure a safe working environment for all employees. Key Accountability The engineer will ensure that we meet the requirements set out in our Quality Management System while ensuring that health and safety is a priority. Ensure that documentation (service reports etc) are completed and stored in the appropriate area within … the QMS and available for audit inspection. - Repairing Anprolene/EOGas sterilisers and purge probes both in-house and on-site - Annual servicing of Anprolene and EOGas Sterilisers in UK and Ireland - Installation of sterilisers in UK and Ireland Servicing and inspections of buildings and grounds are completed on time. more »

Are you an experienced QMS Administrator looking for a part time role? If so, this interesting and flexible role could be just what you are looking for. The Client Established in the UK in 2000, but originally developed in California, USA, our client designs and manufactures a range of PH … renowned companies who are leaders in their specialised field. The Role They are now looking for an experienced QMS Administrator to ensure the Quality Management System processes are established, implemented and maintained. Key Accountabilities Implement and maintain the companys quality management system (QMS) to ensure compliance with ISO 9001 and more »

Responsibilities: This position is responsible for supporting the broad, overall technical operations and customer technical Focus for the company This function includes internal quality management system and external customer technical requirements It is achieved by supporting the head of technical in a broad remit of tasks planned and reviewed across 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 »

join the company. Permanent role with a competitive starting salary and extensive benefits package. Job Overview: Maintenance and improvement of the Quality Management System (QMS). Assure the compliance of all activities with Good Distribution Practice (GDP) and Good Manufacturing practice (GMP) requirements. Responding to medical information enquiries from healthcare 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 »

Key Tasks and Accountabilities Work with the Program/Project Managers and their teams to maintain all aspects of the QMS as we develop our diagnostic capability e.g. Change Controls, Non-Conformities, CAPAs, Customer Complaint Support continuous improvements in the Quality Management System (QMS) and maintain compliance of Quality processes … QA staff, provide support to departments, e.g. reporting on Quality Metrics as well as assisting in training of personnel on matters relating to the QMS and Induction of new starters on Quality aspects. Support Quality department initiatives as required, as part of a multi-disciplinary team Competencies & Requirements for the more »

and prepare comprehensive reports in accordance with design control standards. Background in the medical device sector to understand regulatory requirements and quality management systems (QMS) essential for successful product development. (ISO13485) Knowledge in mechanical engineering with a focus on testing equipment and innovation in product development. Requirements: Bachelor's degree 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 »

support the execution and integrity management. You will be accountable for all Quality activities within assigned work packages, ensuring compliance with contractual requirements, project QMS, regulatory and legal requirements. The Quality advisor promotes and provides professional expert knowledge and guidance to managers, supervisors, and employees on quality practices, safety standards … in focus amongst all contractors, as well as internally in rsted, to achieve this you will: Maintain quality expert knowledge on best practice and QMS requirements Secure quality conformity using agreed processes and registers Support and promote development and use of Orsted management systems Proactive approach to quality risk management more »

and validation processes to prepare the system for clinical studies and FDA approval. Implement test plans and protocols, documenting all activities within the Quality Management System (eQMS). Develop Work Instructions and Standard Operating Procedures (SOPs). Collaborate with Engineering, Manufacturing, and Biology teams to achieve regulatory submission and product more »

burr components. - Running and checking “1st” off and random batch inspection. - Observe machine operation to verify accuracy of machine settings. Technical Understand the Quality Management System Quality Brief. Responsible for the production of Company products. Achieve production targets and deadlines. Work from engineering drawings. To clock in/out and more »

Responsibilities: This position is responsible for supporting the broad, overall technical operations and customer technical Focus for the company This function includes internal quality management system and external customer technical requirements It is achieved by supporting the head of technical in a broad remit of tasks planned and reviewed across more »

of the job About our Pathology Service Specialist Biomedical Scientist Job Information You will enjoy a varied range of responsibilities from maintaining the quality management system and UKAS accreditation, training of less experienced members of staff, validating and authorizing results and most importantly providing safe quality service for our patients. 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 »