Quality Assurance Assistant

Salary negotiable DOE


Do you have experience in Biotechnology Quality Assurance? Are you looking to join an organisation during an exciting time of expansion?

Key Information

  • Yorkshire and Humber
  • 07376 380880
  • Fixed Term, Contract
  • 07-08-2020
  • Salary negotiable DOE

Job Description

An expanding Biotechnology and Diagnostics Company are seeking a Quality Assurance Assistant to join the team at their York site. The company are experiencing growth and there is scope for this initial 6 month Fixed Term Contract to become a permanent role, at either the York or Doncaster Site.

Key Points

  • Initially a 6 month contract , with potential for extension into a permanent role.
  • Based in York, potential to be based in Doncaster as the role progresses.
  • This is an excellent time to join this organisation during a period of expansion.

Main Responsibilities

  • Assisting the Quality manager in the maintenance of all appropriate quality standards, in relation to relevant ISOs.
  • Assist in the maintenance and management of the QMS
  • Carrying out of quality based practices and procedures, such as CAPAs , auditing, training and documentation control.

For more information or to apply, please contact Louis Williams on louis.williams@networkscientific.co.uk.

Due to the volume of applications received on a daily basis, we find it incredibly difficult to respond to each and every one. Should you not hear back from us within two weeks, please assume your application was unsuccessful on this occasion.

Please note that all applicants for this biotechnology job should be able to prove that they are legally entitled to work in the UK. Network Scientific Recruitment, part of Network Scientific Ltd. is an Employment Business/Agency.

To be considered...

  • Have experience with relevant ISOs, particularly ISO9001 and ISO13485
  • Be familiar with relevant quality procedures and controls such as CAPAs, conducting internal audits, approval of Certificates of Analysis, calibration and validation documentation.
  • Experience in a GMP environment
  • Ideally experience in a Biotechnology or Medical Device environment

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