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Colloids Ltd
liverpool, england, United Kingdom
QUALITY ASSURANCE MANAGER LIVERPOOL | SALARY £43,000 - £49,000 DOE WE ARE COLLOIDS LIMITED We are currently looking to recruit a Quality Assurance Manager to join our Quality team based at our headquarters in Liverpool. This role will be reporting directly to the Senior Quality Manager and will interact with all departments across the business. Th
Job Source: Colloids LtdProtein Works
Runcorn, England, United Kingdom
The Role: Quality Assurance Technician This role is based within our head office in Runcorn and has the following main responsibilities:- Releasing product from the production line, including organoleptic assessment of finished product and compare against gold standards Out quality control checks (e.g. CCP, label verification, weights, shift docu
Job Source: Protein WorksGibbs Hybrid Programme Solutions & Consultancy
Moreton, England, United Kingdom
QA Specialist Moreton, GB (Hybrid) 12 Month Contract – Likely Extensions/ permanency £20 per hour Function PDQ Good Manufacturing Practice (GMP) serves as the Quality Assurance Unit overseeing manufacture, testing and distribution of clinical supplies (investigational products) to assure quality and compliance with Good Manufacturing Practices (GM
Job Source: Gibbs Hybrid Programme Solutions & ConsultancyPIB Insurance Brokers
Liverpool
Quality Assurance Manager The role can be based anywhere in the UK we are flexible on Location and there will be an element of hybrid working The Role: The Quality Assurance Manager will develop, manage, deliver, monitor, and report on Quality Assurance throughout the Speciality Division ensuring that processes are current, accurate and in accor
Job Source: PIB Insurance BrokersDamia Group
Wrexham, Wales, United Kingdom
**Senior QA Engineer – Permanent Role – £42,500 Base + Benefits – North East Wales (hybrid)** A HealthTech company are looking to grow their tech team, by bringing on a senior level QA Engineer to work closely with the project and development teams to ensure timely and quality delivery projects. This position is very hands-on role, you will be tes
Job Source: Damia GroupUnipart Logistics
Chester
Location: Broughton and Filton Contract type: Full time Hours: 08:00 - 16:00 Monday to Friday Salary: £28,000 per annum, plus 30 days holiday, pension, life assurance, employee assistance programme, wellbeing support, and flexible benefits scheme About the Job An exciting opportunity has arisen for a full time Quality Compliance Operator with
Job Source: Unipart LogisticsMarstep Resourcing Solutions
Chester
This is a great opportunity to join a fantastic restaurant business, delivering high quality dining and events, where you will have the opportunity to develop a career and feel part of the friendly team from day one.You will work alongside some great people, and the business is only at the start of its expansion, which will mean career progression
Job Source: Marstep Resourcing SolutionsRealm Recruit
merseyside, england, United Kingdom
4+ PQE Unrivalled progression opportunity Hybrid working model – two/three days from home Family feel and close-knit culture This is an outstanding opportunity to join a highly respected and well-established Merseyside law firm as the Head of Conveyancing. Our client prides itself on providing top-quality legal services including private client, f
Job Source: Realm Recruitellesmere port, england, United Kingdom
Here at SRG, we are proud to be partnering with this innovative healthcare company. They are the UK’s leading supplier of mobile facilities that relieve hospital capacity and support vital clinical research. They partner with NHS trusts and private healthcare companies across the UK and offer a wide variety of services.
Due to company growth, they are looking for a quality and compliance leader to come in as their Head of Quality Assurance to oversee all the operational and clinical quality functions within the company. You will be working closely with the COO and managing and building the quality department.
Key Accountabilities:
Build, manage, lead and motivate an integrated, inclusive and flexible team, ensuring that people with the right range of skills and experience are recruited and retained, and that their skills and professional capabilities are maximised.
Provide effective direction, leadership, and development of the quality team (QA and QC) in support of the business as a whole.
Develop, implement and maintain the Quality Management System (QMS) with the Quality Team and take the lead in presenting it to clients in contractual negotiations.
Responsible for the continuing development and promotion of a proactive quality assurance framework across the company.
Provide governance of, and support to ensure ongoing compliance of the Quality QMS with all applicable standards and guidelines in clinical services and clinical trials.
For clinical trials, develop and implement a risk-based and flexible approach to Quality Assurance (QA) within the company, which will ensure that trial participants and data are safeguarded in compliance with applicable regulatory requirements and best practice.
Work with training and monitoring colleagues, to implement, review and maintain tracking of incidents within the organisation, including those related to clinical trials, advising on Opportunities for Improvement (OFI), CAPAs to be implemented and ensure completion in a timely manner.
Ensure systems are in place to support selection and approval of new suppliers of products, materials, and services.
Ensure the production of regular reports and information to the Senior Executive Team and the Board, in relation to regulatory compliance and the performance of the Quality Management System.
To attend and contribute to operational meetings and support events as required.
Working together with the Quality Team to lead, manage and co-ordinate internal and external audits, including regulatory inspections within the company.
As the ideal candidate, you will be a pragmatic leader with experience managing people and teams, as well as critical clinical trials knowledge. You will be a quality assurance expert and have experience of regulations related to clinical services as well as clinical trial regulations, good clinical practice (GCP) guidelines and other frameworks, and their implications for clinical trials research. You will also have experience supporting third party audits and regulatory inspections.
Head of Quality Assurance - Clincial jobs in ellesmere port, england, United Kingdom
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