1 to 8 of 8 Contract QMS Jobs in England

Manager. Familiarize Yourself with ISO 9001 Project Plan Identify Responsibilities, Policies, and Objectives of the Project Develop Your Project Documentation Up to Launch Quality Management System 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 »

the effective deployment of the Integrated Management System (IMS) through internal audits, lead and complete the annual audit schedule, providing assurance that the Quality Management System meets the required standards. Key Responsibilities: Develop and execute a risk-based internal management system audit program compliant with ISO 9001, ISO 14001, and more »

ina clinical pathology laboratory as a Biomedical Scientist Understanding of health and safety legislation pertaining to clinical laboratories Understand the components of a quality management system 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 management more »

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 quality management system 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 Quality Management system 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 Quality Management System to both reduce risk and drive innovation in clinical trial activities and the overall clinical trials service. To ensure all changes to the Quality more »

/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 »