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Quality Manager

DS Recruitment & HR Services
Job LocationOld Dalby
EducationNot Mentioned
Salary£33,000 - £35,000 per annum
IndustryNot Mentioned
Functional AreaNot Mentioned
Job TypeTemporary, full-time

Job Description

Quality Manager (6 months Interim)Salary c£35k dep on experience and benefitsThe Company: Our client is a leading UK based consumer healthcare provider. They supply UK & European retailers with high quality branded and own branded eye / healthcare products. They are looking to appoint a Quality Manager for an initial 6 month cover at their site near Melton Mowbray.The Role: This role is responsible for the maintenance and co-ordination of the Quality Systems. It supports the business in ensuring that it operates in compliance with all relevant quality and regulatory standards.Products are predominantly Medical Devices and Medicinal Products but can also be cosmetics or general products.Key responsibilities and duties include:

  • Maintains the Quality Management System for the company.
  • Supports company production in maintaining its quality standards and resolving issues.
  • Support Technical Manager in ensuring compliance to GDP.
  • Actively looks to improve the Quality Management System in line with new regulatory guidelines, and industry best practice. Maintains Quality improvement plan on behalf of the Technical Manager.
  • Contributes to Quality Systems for Key Manufacturing sites.
  • Maintains the supplier quality audit plan. Carries out audits of suppliers if required.
  • Maintains and implements an internal audit schedule. Ensures all CAPAs have been followed though.
  • Responsible for the change control process.
  • Maintains all quality critical documents eg Quality manuals, SOPs, Quality Policies, Audit Reports.
  • Responsible for Quality Investigation Reports and deviations including the CAPA plan, both at the company premises and those originating at third party suppliers.
  • Responsible for regular reports to senior managers on Quality Key Performance indicators.
  • Ensures any potential quality risks to the business are communicated to senior management and documented appropriately.
  • Co-ordinates recall activities if necessary.
  • Co-ordinates the training of company personnel on GXP requirements that support their functional activities. Maintains training record matrix.
  • Assist in hosting audits from customers and regulatory authorities.
  • Conducts regular reviews of all quality critical documents, systems and procedures to ensure any required changes are made.
  • From time to time may be required to perform additional/different responsibilities in line with your position.
    • The ideal candidate will have:With a background in pharmaceutical manufacturing and a strong understanding of current GMP and technical processes you will consider yourself to be highly motivated and a natural leader.
  • Science or Life Science Graduate or equivalent level with at least 3 years Quality Management experience within a regulated healthcare environment.
  • Excellent understanding of regulations supporting healthcare product development, ie GMP, GDP, Medical Device, ISO 9001, ISO 13485, BRC, HACCP.
  • Familiar with Product Development Lifecycle and its processes.
  • To be a proactive problem solver.
  • To be able to work as part of a team and develop self and others.
  • To share their knowledge and experience with others.
    • Key phrases: Quality Manager, QA, HACCP, Melton Mowbray Required skills
  • GDP
  • GMP
  • QA
  • HACCP

    • Keyskills :
    GDP GMP QA HACCP

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