1 to 25 of 34 QMS Jobs in the East of England

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 »

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 »

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 »

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 »

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 »

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 »

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 »

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 »

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 »

a high profile Wind Farm project. 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 place to reduce the cost of poor quality and non-conformances within the project Duties Maintain quality expert knowledge on best practice and QMS requirements Supports the development and implementation of project quality assurance, management and control strategy Provides Quality support and direction to the Project team for assigned 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 »

machines to manufacture precision components. Technical Adhere to Health and Safety regulations and law. Have knowledge of ISO9001, ISO14001 and Q1. Understand the Quality Management System Quality Brief. Responsible for the production of Company products. Achieve production targets and deadlines. Work from engineering drawings. Check materials for type and quantity. 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 »

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 »

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 »

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 »

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 »

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 »

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 »

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 »

and processes regularly. Maintain and align HACCP (HACCP/TACCPVACCP) program is maintained and aligned with best practice at all times Implement and amend QMS for product standards. Ensure effective QA and Hygiene team management. Implement pest control mechanisms for food safety. Conduct trend analysis of quality issues. Manage internal more »

ready to step up into a Principal role or an established PA looking for a change in their career. The Role: Adherence to the QMS including root cause analysis and communicating with clients on technical matters. Assistance in maintenance programs for the Departments specific analytical instrumentation and any other analytical more »