Swadlincote, Derbyshire, East Midlands, United Kingdom Hybrid / WFH Options
Omega Leeds
Manager. Familiarize Yourself with ISO 9001 Project Plan Identify Responsibilities, Policies, and Objectives of the Project Develop Your Project Documentation Up to Launch QualityManagementSystem Review Performance Register for Certification Continual Improvement activities Key Responsibilities – Project Manager Quality Systems Promote Health and Safety in the workplace above everything else more »
Bridgwater, Somerset, South West, United Kingdom Hybrid / WFH Options
Mactech Energy Group
the effective deployment of the Integrated ManagementSystem (IMS) through internal audits, lead and complete the annual audit schedule, providing assurance that the QualityManagementSystem meets the required standards. Key Responsibilities: Develop and execute a risk-based internal managementsystem audit program compliant with ISO 9001, ISO 14001, and more »
scope to progress the job eg may entail a small amount of work not immediately inside of the CSV arena. Knowledge of Trackwise electronic QMS would be advantageous. If you are interested in this role, please apply. Please visit our website to find out more about our Key Information Documents. more »
Lancashire Teaching Hospitals NHS Foundation Trust
ina clinical pathology laboratory as a Biomedical Scientist Understanding of health and safety legislation pertaining to clinical laboratories Understand the components of a qualitymanagementsystem Desirable Problem solving ability Understanding of laboratory quality issues Familiar with pathology LIMS Good knowledge of immunological processes in health and disease Qualifications Essential 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 managementmore »
Bolton, Greater Manchester, North West, United Kingdom
Expleo Group
Role Overview : We are seeking a highly motivated and skilled Electronic Design Engineer to join our dynamic team in Bristol. The successful candidate will be responsible for the design, development, and validation of electronic systems and subsystems for our advanced more »
coordinating IMP supply and eventual closure and archiving of the trial To be responsible for ensuring the requirements of the production area's qualitymanagementsystem are maintained and developed as required by the MS(specials), MIA(IMP) licenses and NHS guidance. To deputise for the Senior Production Pharmacist - Clinical … in accordance with data integrity principles to be audit ready at all times. Governance and Quality To ensure that the Clinical Trial Pharmaceutical QualityManagementsystem is maintained and developed in accordance with the MS(Specials) and MIA(IMP) license requirements and in response to changes in regulations and legislation. … quality and final product disposition from a production perspective in liaison with QA and the QP. To support and document change through the QualityManagementSystem to both reduce risk and drive innovation in clinical trial activities and the overall clinical trials service. To ensure all changes to the Qualitymore »
Procedures, Training Instructions and Batch Records. This includes document review and approval. Perform CAPA Coordinator activities; coordination Quality Incidents and Deviations within a QualityManagementSystem (Agile. Proactively contributing to continuous improvement initiatives and other general housekeeping duties. Taking a self-motivated approach to continuous professional development and engaging with more »
Cheltenham, Gloucestershire, South West, United Kingdom
Jefferson Wells
/Warehousing Team in daily Dock to Stock Processing. Receive, verify, process and receipt goods to the business system. Process through the Quality database (QMS) Record supplier C of C's/Pack slips Communicate queries through to appropriate person. Transact, verify and locate Inventory. Comply with Stores Procedures Physical more »
and Qualifications: Demonstrated experience in the design and development of products - Medical industry advantageous Design or Engineering Degree preferred Familiarity with regulatory standards and QMS - ISO13485 advantageous CAD proficient, preferably Solidworks Plastic manufacturing process knowledge If you want to be part of a team dedicated to making a meaningful impact more »
still be able to apply on the basis that you can obtain the tickets before starting. Responsibilities • Support the implementation of the Project QualityManagementSystem (PQMS) on the vessel •As the QC Co-ordinator, you will support Project Quality Manager (PQM) supervising the Quality Control activities on the vessel more »
on a 12-month maternity cover contract. As a Senior Quality Engineer, you will play a pivotal role in maintaining and enhancing the qualitymanagementsystem, ensuring compliance with industry standards and regulations, and driving continuous improvement initiatives across our operations. Key Responsibilities: Lead the implementation and maintenance of the … qualitymanagementsystem in accordance with AS9100 and other relevant standards. Conduct audits and assessments to identify areas for improvement and ensure compliance with regulatory requirements. Develop and implement quality control procedures and protocols to monitor product quality throughout the manufacturing process . If this sounds like something of interest more »