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QC Analystck group • Neuchâtel
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QC Analyst

QC Analyst

ck group • Neuchâtel
Vor 12 Tagen
Stellenbeschreibung

QC Analyst

CK QLS is recruiting four Quality Control Analysts to support a pharmaceutical QC laboratory in Switzerland. This is an opportunity for experienced laboratory professionals who enjoy hands-on biochemical testing and take pride in accurate, well-documented work.

The roleYou will carry out biochemical analyses in a cGMP environment, working to established laboratory procedures and quality standards.

Your responsibilities will include:

  • Performing routine testing using techniques such as ELISA, HPLC, electrophoresis, PCR, Western blotting or enzyme activity assays.
  • Preparing laboratory solutions and checking that equipment calibration and maintenance are up to date before use.
  • Recording results accurately in forms and logbooks in line with Good Documentation Practice and ALCOA+ principles.
  • Escalating invalid or out-of-specification results promptly and supporting laboratory investigations.
  • Executing reagent and consumable qualification protocols and supporting method, system and equipment validation.
  • Maintaining an organised laboratory in line with 5S standards and contributing to continuous improvement.

About you

  • A CFC in laboratory science or biology, or another relevant scientific qualification.
  • At least three years’ experience in a pharmaceutical QC laboratory working under cGMP.
  • Practical experience with biochemical analytical methods. Experience in electrophoresis, HPLC, ELISA or enzyme activity testing is particularly relevant.
  • A structured, careful approach to laboratory work, with a strong focus on data accuracy, documentation and compliance.
  • The ability to stay engaged and maintain high standards when carrying out routine analyses.
  • Confidence working in a busy laboratory where priorities can change quickly, along with the judgement to flag issues promptly.
  • Fluent French and sufficient technical English to understand laboratory procedures and documentation.
  • Experience writing method validation protocols would be an advantage.

Applicants must be Swiss or EU citizens, or hold a valid Swiss work permit.

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QC Analyst • Neuchâtel