QC SCIENTIST

Michael Page Switzerland

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  • Publication date:

    26 February 2024
  • Workload:

    100%
  • Contract type:

    Temporary
  • Place of work:

    Switzerland

To be responsible for managing the life cycle of analytical tests carried out in the quality control department

QC SCIENTIST

Our client is one of Switzerland's leading biotech companies

Description

Validation and Qualification Activities
* Author transfer protocols and reports for assays
* Author qualification plans and reports for critical reagents
* Oversee validation and qualification activities executed by analysts, provide training and support
* Execute and documents experiments

Investigation Leads
* Investigate and trouble shoot problems which occur to determine solutions or recommendations for improvements or change
* Conduct/participate in risk assessments, root cause analysis and investigations
* Own Laboratory Investigations and CAPA

Quality Control Support Activities
* Support the application of industry specific compliance standards/regulations to assays life cycle management activities
* Participate to daily activities upon request (provide technical and statistical support)

Profile

* University or engineering degree in analytical chemistry, biotechnology, biochemistry
* 1 or 2 years of experience in GMP pharma business activities, preferably in the scope of recombinant therapeutic product in pharmaceutical environment
* Experience in GMP Laboratory activities
* Good knowledge of method transfer
* Good knowledge of critical reagent qualification
* Experience in problem solving and deviation management
* Good Knowledge of statistical tools
* Fluent in French and English (C1 written and spoken)

Job Offer

* Laboratory Investigations
* Critical Material Qualification
* Laboratory Method Transfers

Contact

  • Michael Page Switzerland

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