QC Analyst

Job description

Job responsibilities;

  • The QC analyst will be working as directed by the Area Supervisor, in accordance with Company safety policies, cGMP and cGLP.
  • Receiving and logging samples into the Laboratory.
  • The QC Analyst will be responsible for analysing raw material, in-process, finished product and stability samples according to specifications, primarily HPLC and dissolution.
  • Analysing validation samples according to validation protocols and investigational samples as directed.
  • Recording results in a timely and accurate fashion.
  • Ensuring the Right First Time KPI with respect to Quality Control Analyst’s documentation are achieved.
  • Reviewing co-workers/analyst documentation
  • Ensuring that all Quality Systems within the department are adhered to on a daily basis.
  • The QC Analyst will be responsible for troubleshooting any OOS analytical data obtained and assisting with laboratory investigations
  • Helping to ensure laboratory SOPs and specifications are kept up to date and in a state of compliance.
  • Training other laboratory staff as requested and appropriate.  

Job requirements;

  • A BSc Degre in conjunction with at least 18 months' work experience working within a pharmaceutical cGLP environment.
  • A minimum of 12 months working experience of HPLC & GC testing methods.
  • Possessing excellent attention to detail is a must with ability to critically review analytical data.
  • Ability to troubleshoot, identify analytical issues and follow up with corrective actions
  • Knowledge of validation and tech transfers is desirable

Following your application for this specific role, Sigmar may contact you regarding other positions that we feel you may be suitable for. If you do not wish to be contacted about other opportunities please let us know. For further information please refer to the Privacy Statement on our website.