QC Associate Scientist.

Job Details

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Job Details

For our client, an international company based in Neuchâtel, we are looking for a QC Associate Scientist

General Information:

  • Workplace: Neuchâtel

  • Contract : Temporary, one year

  • Start date : January 2025

  • Workload: 100%

 

Tasks and responsibilities:

The job holder is accountable for life cycle management activities of analytical assays performed in the QC Laboratories of Neuchâtel – 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, policies and EHS

  • requirements.

 

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, microbiological

  • 1 or 2 years of experience in GMP pharma business activities, preferably in the scope of recombinant therapeutic product in pharmaceutical environment

  • Fluent in French and English (C1 written and spoken)

  • 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

 

Competencies

  • 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

For our client, an international company based in Neuchâtel, we are looking for a QC Associate Scientist

General Information:

  • Workplace: Neuchâtel

  • Contract : Temporary, one year

  • Start date : January 2025

  • Workload: 100%

 

Tasks and responsibilities:

The job holder is accountable for life cycle management activities of analytical assays performed in the QC Laboratories of Neuchâtel – 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, policies and EHS

  • requirements.

 

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, microbiological

  • 1 or 2 years of experience in GMP pharma business activities, preferably in the scope of recombinant therapeutic product in pharmaceutical environment

  • Fluent in French and English (C1 written and spoken)

  • 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

 

Competencies

  • 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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LS

Luciana Sardo

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