Scientist - Quality Control

SThree_Germany

Ansprechpartner: Andrey Lobov
Neuchâtel,  Schweiz
Vor OrtArbeitnehmerüberlassungStart 12/2026

Beschreibung

Scientist - Quality Control (French Speaking)

Location: Neuchâtel, Switzerland
Contract Type: Temporary contract
Contract Duration: 9 months
Start Date: 1 December 2026Position Overview

The Scientist is accountable for life cycle management activities relating to analytical assays performed in the Quality Control Laboratories in Neuchâtel, Switzerland, with a particular focus on:
  • Laboratory investigations
  • Critical material qualification
  • Laboratory method transfers


In addition, the Scientist supports daily Quality Control activities in accordance with cGMP requirements, and Environmental, Health and Safety requirements.Key Responsibilities

Validation and Qualification Activities

  • Author transfer protocols and reports for analytical assays.
  • Author qualification plans and reports for critical reagents.
  • Oversee validation and qualification activities executed by analysts.
  • Provide training and support to analysts.
  • Execute and document experiments.
Investigation Leadership

  • Investigate and troubleshoot problems to determine appropriate solutions or provide recommendations for improvements or changes.
  • Conduct and participate in risk assessments, root cause analyses, and investigations.
  • Take ownership of laboratory investigations and Corrective and Preventive Actions.
Quality Control Support Activities

  • Support the application of industry-specific compliance standards and regulations to assay life cycle management activities.
  • Participate in daily Quality Control activities upon request.
  • Provide technical and statistical support.
Education and Professional Experience

  • University or engineering degree in analytical chemistry, biotechnology, or biochemistry.
  • One to two years of experience in GMP pharmaceutical activities, preferably involving recombinant therapeutic products within a pharmaceutical environment.
  • Experience in GMP laboratory activities.
  • Good knowledge of method transfers.
  • Good knowledge of critical reagent qualification.
  • Experience in problem-solving and deviation management.
  • Good knowledge of statistical tools.
  • Fluent French and English, with a minimum C1 level in both written and spoken communication.
  • Proficiency in all aspects of standard IT tools.
Competencies

  • Excellent collaboration skills and a strong teamwork mindset.
  • Good troubleshooting and problem-solving skills.
  • Ability to work independently in a fast-paced environment.
  • Ability to manage multiple priorities and recognise when issues need to be escalated for resolution.
  • Effective communication skills.
  • Demonstrated ability to synthesise information.
  • Demonstrated ability to give and receive feedback.


SThree_Germany is acting as an Employment Business in relation to this vacancy.

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