21/03/2024 | Fulltime | Morpeth | Piramal Pharma SolutionsAnd stakeholders on IT quality principles, practices, and regulations.* Review and approve changes to IT data processes, and documentation to ensure data integrity and compliance with regulatory requirements.* Manage IT projects, ensuring compliance with GMP guidelines, regulatory requirements, and industry
Save for later24/04/2024 | Parttime | Cambridge | CV-LibraryOf new creative practices to enable efficient application and adoption of safety processes. Deliver high-quality documentation, i.e., reports and work products, according to industry standards, groundbreaking methodologies, tools, and templates. Keep up to date with Functional Safety Standards
Save for laterRegister your CV24/04/2024 | Fulltime | Cheshire | CV-Library | £15 / Hour Medical Devices/ Pharmaceutical Industry is preferred. Understanding of compliance with FDA and European regulations relating to Quality Systems (ISO134852016, ISO90012000, FDA 21 CFR part 820) and GMP Guidelines and Regulation. Good working knowledge of Microsoft Office, specifically Word and Excel
Save for laterRegister your CV24/04/2024 | Fulltime | Bristol | CV-LibraryOf any risks or issues that could impact the outcome of the project, to prevent potential customer or business impacts. - Undertake and oversee User Acceptance Testing to ensure accuracy of system changes made during a project. - Produce detailed project documentation. Also, carry out analysis to create
Save for laterRegister your CV24/04/2024 | Fulltime | Staffordshire | CV-Library | £90,000 - £100,000 / Year For distribution, ensuring compliance with all relevant regulations and guidelines. 3. As the Qualified Person you will participating in internal and external audits of the manufacturing facilities and quality systems. Providing expertise and guidance on regulatory requirements and quality standards to internal
Save for laterRegister your CV24/04/2024 | Fulltime | Ipswich | CV-Library | £13 / Hour In the manufacturing process according to the standard required in SOP documents, meeting targets for cycle time and quality and ensuring safety guidelines are followed at all times. Operating a variety of different types of Fab - Test Equipment - optical vision systems, manual and automated devices as well as the use
Save for laterRegister your CV24/04/2024 | Fulltime | South Yorkshire | CV-Library | £90,000 - £100,000 / Year For distribution, ensuring compliance with all relevant regulations and guidelines. 3. As the Qualified Person you will participating in internal and external audits of the manufacturing facilities and quality systems. Providing expertise and guidance on regulatory requirements and quality standards to internal
Save for laterRegister your CV24/04/2024 | Fulltime | Preston (Lancashire) | CV-Library | £48,000 - £56,000 / Year Commitment to Kanban and Kaizen management systems. Production control with KPI's reported and ownership of the Production department. Utilising your strong leadership qualities and providing motivation, support, mentoring and guidance to all employees whilst being a confident and approachable leader
Save for laterRegister your CV24/04/2024 | Fulltime | Norwich | CV-LibraryEnsure the proper and accurate use of all systems to search and order parts Complete all required documentation accurately and promptly Deal with all cash and credit card transactions in line with TPS Guidelines in the Operations Manual What are we looking for? A self-starter with a proven track record
Save for laterRegister your CV24/04/2024 | Fulltime | Golborne | CV-LibraryDeveloping further within the role of project management. Duties and Responsibilities Ability to work collaboratively within a team and assist with all aspects of project delivery; Assist with preparing and maintaining project documentation, including Risk Register, Issue Register, Daily Log, Project
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