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.
  • 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 (Involvement in Lab Investigations Reports)

Job requirements;

  • BSc. Degree in science or a related discipline with at least a years’ experience working within a pharmaceutical lab.
  • Must be familiar cGLP and have experience working with HPLC.
  • The QC analyst will have excellent attention to detail and have experience with troubleshooting and corrective actions.

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