Quality Control Scientist

vor 3 Wochen

Neuchatel, Schweiz Randstad Vollzeit
For our client, an international company in Neuchâtel, we are looking for a 
QC Associate Scientist.
  • Start date:ASAP
  • Contract: for 6 months via Randstad 
  • Extension: possible
  • Workplace: Neuchâtel
  • Workload: 100%


    Responsibilities:

    The job holder is accountable for life cycle management activities of analytical assays performed in the QC.
    Laboratories of Neuchâtel â Switzerland with a focus on:

    • Laboratory Investigations
    • Critical Material Qualification
    • Laboratory Method Transfers

      In addition, the job holder also supports daily QC activities following cGMP, and EHS requirements.

      Daily activities:

      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)


            Your 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)
            • Proficiency in all aspects of standard IT tools
            • Excellent collaboration skills and teamwork mindset
            • Good trouble shooting and problem-solving skills
            • Ability to work independently in a fast-paced environment
            • Ability to manage multiple priorities and know when to escalate issues for resolution
            • Effective communicator
            • Demonstrated ability to synthesize information
            • Demonstrated ability to give and receive feedback

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