• Independent multi-sector recruitment specialist

Quality & Compliance Engineer

Role Type: Permanent

Location: Cambridge, Cambridgeshire,

Salary From: £45000

Salary To: £52000

Contact Name: Major Recruitment

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A Quality & Compliance Specialist is needed by a growing engineering company near Cambridge

The role involves responsibility for SOP’s, Documentation and Quality Management Systems and will include the following duties:-

  • Compilation and Issue of all Standard Operating Procedures.
  • Detailed and individualised SOP’s in place for all major work tasks in each department, relevant, specific and approved.
  • Compilation and upkeep of all Policy documents, reviewed and revised annually.
  • Full suite of accurate and reflective policies that protect the company fully.
  • Implementation and upkeep of all documents required for the quality management system.
  • Ensure ISO9001 is in place every year with no lag in accreditation membership.
  • Review all QMS documents of another large company and make sure our policy documentation is in line.
  • Ensuring all ISO requirements are fulfilled during the year, managing the process of ISO9001 and conducting the audit.
  • Attending Supplier manufacturing sites and conducting quality audits following due process and recording via approved documentation.
  • Controlling the Master Project Folder, reviewing each project folder and ensuring all relevant documents have been stored and are filed in the correct location.
  • Review the manufacturing process and support where necessary to document and improve upon this process.
  • Review the design process and ensure that design translates to manufacturing well enough, improve where possible.
  • Inspect all manufactured goods and packaging, ensure that it is fit for purpose and approve for delivery.
  • Influence the creation of the assembly instructions and ensure that these are functional, user friendly, translatable and will not create confusion or gaps in the installation process.* Build and release technical file for the client
  • Compiling and executing snag lists using site audit pro.
  • Sharing with the PM and setting a timeframe for return to review and close out the list.
  • Providing support to rectify contentious issues.
  • Liaising with suppliers, sub-contractors and direct employed resource to outline the snags and ensure rectification and continuous improvement for future jobs.
  • Implement training or build codes of practice documents where required to ensure work is to a consistently high quality.

The successful candidate will have experience of managing Quality Management Systems within the Process Manufacturing sector and ideally come from a Pharmaceutical Background. You will also need an in-depth knowledge of ISO9001 systems Experience of building and executing Commissioning documentation is essential as are good communication and interpersonal skills and the ability to manage stakeholder expectations

This is a varied and interesting role within a growing engineering company. Please call Adam Jones at Major Recruitment or click Apply Now if you would like to know more

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