Scientific
Scientific

Quality Administrator

Liverpool

Scope

This is a fantastic opportunity to join an established pharmaceutical company as part of the Quality Assurance team at their impressive site just outside of Liverpool. As a quality administrator, you will be responsible for administrating document control activities to support the QA function.

The QA function is to design, implement and monitor Quality systems for pharmaceutical GMP, manufacturing, quality control and batch review and release. In this role, you will have the opportunity to develop your experience within QA document control in a flexible and dynamic working environment.

Responsibilities

Implement Quality systems in line with company requirements:

  • QA Team participation.
  • GMP document control and administration
  • Provide document creation support ensure all documents are formatted to company procedures by assisting the document owner with reformatting where required.
  • Generation and management of documents and SOPs within the quality Management Systems
  • Assist in the creation and generation of quality documentation as required.
  • Control and issue of document and logbook numbers and document the return and destruction of controlled documents and logbooks

About You

To apply, you must have prior experience with GMP documentation, ideally in a pharmaceutical setting, in addition to the following:

  • Experience of GMP pharmaceutical quality systems
  • Ideally prior experience with electronic document systems
  • Good attention to detail and literate
  • Good communication skills
If you are interested in the above role then please apply or get in touch to discuss further.
Ed Curl Managed by Ed Curl
highlights
North West
Contract
Office
apply Posted - 08.02.2021

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Consult will endeavour to contact candidates within 14 days of application. However, if you do not hear back after 2 weeks then please assume on this occasion, unfortunately, you have not been successful.