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QC Stability Co-ordinator

  1. London
Liverpool
  1. Contract
Competitive
  1. CAPEX Projects
34361
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QC Stability Co-ordinator - 6-month contract initially - Liverpool 

Our client is a global biopharmaceutical company manufacturing plasma-derived, and recombination therapeutic products, who in turn deliver high-quality medicines that treat people with rare and serious diseases, and we are now searching on an exclusive basis with the client to appoint a QC Stability Co-ordinator to join their busy and rewarding team on a contractual basis for a period of 6-Months.


Key responsibilities:
  • To author stability protocols, interim reports, and reports for stability studies. This includes routine campaign stability studies and non-routine project stability studies.
  • Management of stability studies in accordance with internal procedures, ensuring studies are set up per the protocol. Will liaise with relevant QC laboratories to ensure stability samples are tested within their specified time frame.
  • Trending of stability data through data table management and trend analysis utilising specialist software. To escalate any trends to the QC Stability Team Coordinator and support any investigations as required. Will support the business in requests relating to stability data (including, but not limited to temperature excursion assessments, regulatory requests and investigational work).
  • To own and support stability related Deviations, CAPAs and Change Controls, and progress department improvements as appropriate.


Experience required:
  • Science related degree
  • Proven GMP background in the pharmaceutical industry
  • Experience of Quality Control testing techniques and industry practices
  • Proven time management skills for planning and schedule of work
  • Proven communication skills both written and verbal
  • Strong Microsoft excel skills
  • Analytical Mindset
  • Science related degree
  • Exp in data trending / software packages (JMP) desirable

If this role is of interest to you, please apply now! 

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