• Adhering to the principles of GMP including good documentation practices.
  • Performing laboratory write-ups.
  • Ensure all raw data is archived according to established procedures.
  • Writing, updating and reviewing methods, specifications, protocols, certificates of analysis and reports.
  • Ensuring laboratory equipment is calibrated and maintained and data are backed-up according to established procedures.
  • Performing analysis using HPLC and GC mainly and other techniques such as UV, IR and wet chemistry.
  • Will have a BSc or equivalent in a Chemistry degree.
  • Must have previous experience with HPLC, GC, wet chemistry techniques, UV and IR.
  • Must have experience testing pharmaceutical products in a GMP environment.

JD for QC Analyst Recruitment Agency in London, Pharmaceutical Recruitment Agency in London