Scientist - Quality Control
SThree_Germany
Ansprechpartner: Andrey Lobov
Neuchâtel, Schweiz
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:
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
SThree_Germany is acting as an Employment Business in relation to this vacancy.
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.
- 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.
- 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.
- 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.
- 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.