QC Scientist

QC Scientist - Analytical Methods Transfer & Life Cycle (m/f/x)

Location: Neuchâtel, Switzerland

Contract type: Temporary assignment via Randstad (approx. 9 months with possibility to extend, starting December 2026)

Work rate: 100% (40 h / week)

Sector: Pharmaceutical Industry / Biotechnology

Job Description

For a leading biopharmaceutical production site located in the canton of Neuchâtel, we are looking for a QC Scientist.

Reporting to the Quality Control laboratory, you will be responsible for activities related to the life cycle of analytical methods, with a strong focus on method transfers, qualification of critical reagents and laboratory investigations, in strict compliance with GMP / cGMP.

Main tasks

• Validation and Qualification:
• Write protocols and reports for analytical method transfers.
• Develop qualification plans and reports for critical reagents.
• Supervise qualification and validation tests carried out by technicians/analysts; provide technical support and training.
• Perform and document experiments in compliance with data integrity rules.

• Investigation management and problem resolution:
• Lead and participate in laboratory investigations (OOS / OOT), risk analyses and root cause investigations.
• Define, open and follow up corrective and preventive action plans (CAPA).
• Resolve technical malfunctions encountered on methods and propose continuous improvement actions.

• Technical support to the quality control laboratory:
• Ensure compliance of activities with current regulatory requirements (Pharmacopoeias, cGMP) and site EHS standards.
• Provide technical and statistical assistance to routine teams as needed.

Profile sought

• Education: University degree or engineering diploma (Master / MSc) in analytical chemistry, biotechnology, biochemistry or related discipline.
• Experience:
• 1 to 2 years of experience in a pharmaceutical/biotechnological GMP environment (preferably on recombinant proteins / therapeutic products).
• Practical experience in QC laboratory activities, analytical method transfers and qualification of critical reagents.
• Proven experience in managing analytical deviations and using problem-solving tools.
• Technical skills: Good command of statistical tools applied to analysis and ease with common IT tools.
• Languages: Fluent in French and English (C1 level written and spoken essential).

Required qualities

• Strong team spirit and excellent interpersonal communication skills.
• Scientific rigour, pragmatism and proven problem-solving ability.
• Autonomy, sense of priorities and adaptability in a dynamic environment.
• Ability to summarise and openness to constructive feedback.