QC Professional (£13.11 – £18.89 per hour)

Our client a High tech, dynamic Biotech company, based in Speke is looking for a QC Professional from a Pharmaceutical background to join their Quality team.

This role is to start as soon as possible and to last for 3 months (possible longer). There is also a possibility of other opportunities arising from the position for the right candidate.

The role is paying between £13.11 – £18.89 dependant on experience.

****Please do not apply for this role unless you are available immediately/on a 1 weeks notice AND are able to commit to shift work ****

Working patterns will vary dependent on the area but will be a mix of:
Days (Monday - Thursday 8am - 4.45pm, Friday 8am - 1pm) paying between £13.11 - £14.20 per hour
Shift 1 - Days 2 on 2 off (hours depend on area) the rate will range from £16.00 - £17.32 per hour
Shift 2 - 2 days 2 nights, 2 on 2 off - £17.44 - 18.89 per hour.

Key Responsibilities

  • Perform raw material and components inspection (quality receipt) and sampling.
  • Communicate their findings as a result of testing promptly, to the QC Analytical leadership team (Team Coordinators and Manager).
  • Highlight deviations (either out of specification results or compliance gaps) to a leadership team member immediately as they are recognised.
  • Instrument Maintenance and Calibration
  • Sampling booth cleaning and monitoring
  • Reagent and Standard Qualification
  • Initiation of deviations
  • Initiation, and completion, of CAPAs
  • Completion of Change Control actions
  • Updates and reviews of SOPs
  • Participation in quality risk assessments
  • HSE risk assessment completion, review and adherence
  • Archiving of laboratory documentation,
  • Ordering of reagents and consumables
  • Maintenance of QC sample and reagent stores
  • Ensuring a clean and safe workplace for all associates
  • Proactively maintain their own training records, and to only perform tasks that they have confirmed themselves to be compliantly trained in, in accordance with local SOPs
  • Communicate professionally and effectively with their fellow team members and the QC Analytical leadership team.

Key Skills/Experience:

  • Must be fluent in English as the primary operating and reporting language used within the industry
  • Have experience in QC testing techniques appropriate to their role
  • Have experience in cGMP application
  • Have an awareness of the requirements for equipment and method validation
  • Have awareness of root cause analysis
  • Be computer literate and be able to demonstrate an understanding of electronic systems
  • Must be educated to NVQ level 2 or equivalent in a relevant scientific discipline
  • Must have experience in the relevant testing discipline, ideally within the pharmaceutical industry having worked to cGMP standard

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