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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 WorksPIB 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 BrokersSRG
ellesmere 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
Job Source: SRGUnipart 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 LogisticsImperial Workforce
Liverpool
Quality Representative Imperial Recruitment Group are delighted to announce that we are working in partnership with a Teir 1 Automotive Manufacturer who are recruiting for a Quality Representative on a Permanent basis. Salary: Negotiable Contract Type: Permanent Location: Solihull or Liverpool Hours: Full time Responsibilities: You will work on-sit
Job Source: Imperial WorkforceWabtec Corporation
Birkenhead, England, United Kingdom
Who will you be working with? As a Quality Engineer, you will play a pivotal role in ensuring the quality and compliance of engineering components. You will be responsible for the investigation of customer returns and warranty claims through examination of parts and products to determine if warranty claims are valid. Role: Quality Engineer Salary
Job Source: Wabtec CorporationRRxCo.™
Deeside, WALES, United Kingdom
RRxCo is partnered with a UK-based business established in 2010 focusing on antibody, protein and peptide drug conjugate medicines and technology. The bioconjugation team was formed in 2011 and moved into a state-of-the-art facility in 2018. The facility has been built for containment; with the safety of their people and the environment in mind, an
Job Source: RRxCo.™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 (GMP) and other applicable regulations and internal procedures.
Key responsibilities include drug substance and drug product batch disposition (release/reject decision), product certification and release by the UK/EU Qualified Person, and audit of internal GMP systems/processes and suppliers/third party contractors, as well as assist stakeholders with regulatory advice and preparation for and management of regulatory agency inspections.
Primary Responsibility:
Review and label vendor specifications in accordance with relevant regulatory requirements for assigned projects.
Review and approve vendor generated label proofs/specifications and other related documents.
Utilizes electronic verification software to perform check on label proof. Routes final label for review and approval accordingly.
Work cross-functionally with individuals and project teams.
Other Responsibilities
Performs specific quality related functions such as Quality/GMP training, materials/products releasing, validation, quality incident investigations to ensure compliance with GMP regulations and standards.
Supports in the investigation of non-conformances and quality incidents. Resolves and documents any deviation or problem pertaining to the audit of documents.
Reviews and approves documents related to Quality Systems such as validation protocols/reports, change control, or Procedural Documents to support the release function.
Support internal and/or external audits as required.
Participates in assigned training including GMP and safety training.
Ensures regulatory, GMP, GDP compliance of activities in assigned areas of responsibility. Reports any deviations to the appropriate management.
Liaises with responsible Trial Supplies Manager on aspects of clinical supplies packaging and labelling design and study requirements and resolves issues.
Competencies Required:
Ability to plan, manage and execute multiple projects and to deliver against critical timelines in a fast-paced, rapidly changing environment.
Attention to detail and a strong ability to concentrate
Exceptional project management skills and detail oriented.
Possesses solid oral and written communication skills.
Good decision making and organizational skills.
Ability to effectively communicate ideas and to influence others to achieve results.
Ability to understand and apply regulatory and CGMP principles.
Good understanding of pharmaceutical or medical terminology
Proficiency in standard office technology, including Microsoft Suite (Outlook, PowerPoint, Excel) Additional applications such as Adobe. Willing to learn additional applications as needed.
Experience working on multi-disciplinary teams and projects.
Good knowledge of rigorous pharmaceutical and/or scientific documentation practices and change control processes (e.g., revision control) is preferred.
Experience:
Bachelor's degree or equivalent in pharmacy, engineering, or life sciences.
Relevant experience in the pharmaceutical industry or related healthcare environment.
Labelling experience in the pharmaceutical industry is highly desired.
If you are interested, please do not hesitate to apply! Either apply direct or reach out [email protected]
Quality Assurance Specialist jobs in Moreton, England, United Kingdom
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