Quality Control Analyst - GMP, Biochemistry

Project overview

Job opening for Quality Control Analyst - GMP, French, Biochemistry for our client based in Neuchâtel in the Pharma sector.

Responsibilities

You bring solid laboratory experience, including biochemical methods such as ELISA, PCR, enzymatic activity, Western Blot, HPLC, or others.

In particular, we expect:

Your experience/knowledge:

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• You work in a structured manner and with a focus on quality.
• You find satisfaction and motivation in routine tasks.
• You have experience with Good Manufacturing Practices (cGMP) and laboratory practices.
• Quality control in the pharmaceutical industry.
• We favor a close-knit and relaxed environment. The work is carried out within a team where tasks change very rapidly. We therefore expect you to be motivated by a rapidly evolving environment while being able to deliver high-level results.
• Main missions:
• - Perform biochemical analysis activities and supervision according to current procedures in the laboratory, respecting GMP/GDP rules and/or projects related to the activities of the Quality Control department.
• - Prepare solutions used for our laboratory analyses.
• - Respect all current procedures.
• Respect and apply EHS rules.
• Fill in various forms, logbooks, and documents in compliance with Good Manufacturing and Documentation Practices and ALCOA+.
• Inform the Supervisor immediately of any non-conforming and/or invalid results, orally and/or in writing, and initiate the event in the quality system within the given deadlines.
• Manage laboratory investigations.
• Apply planning requests and proactively report any issues.
• Execute qualification protocols for reagents/consumables and validation (method, system, equipment).
• Ensure that equipment calibration and maintenance are in order during analysis.
• Respect real-time Kanban management.
• Report deviations from procedures to the method/equipment manager and the Supervisor/delegate/Expert.
• Be able to identify and resolve minor issues related to your area of expertise (Troubleshooting).
• Prepare or approve solutions in the laboratory.
• Manage and organize the laboratory in general, respect 5S standardization norms.
• Support continuous improvement initiatives.
• Training such as a CFC in laboratory technology in biology or another relevant scientific field.
• Minimum 3 years of experience in a quality control laboratory in a cGMP environment.
• Desired experience in electrophoresis, HPLC, ELISA, and/or determination of enzymatic activity.
• Good understanding of laboratory practices, quality requirements, and EHS standards.
• Language skills: French, English

Project details

Neuchâtel, Switzerland

Work mode: On-site

Sector: Pharma

As soon as possible

9+ months

100%

Ref. No.: BH 24744

If you wish to apply, please send us your CV along with a phone number where we can reach you during the day.

Due to work permit restrictions in Switzerland, we can only consider applications from Swiss nationals, EU citizens, and current holders of a Swiss work permit.

We accept applications from people of all genders, ages, sexual orientations, personal expressions, ethnic origins, and religious beliefs. Therefore, it is not necessary to provide information about your gender or a photo in your application.

In accordance with client requirements, we need information about your marital status, nationality, date of birth, and a valid Swiss work permit. For candidates with disabilities, we are happy to explore potential solutions with our end client.

• Start: 2026-10
• Remote: onsite
• Location: Neuchâtel, Schweiz, CH
• Languages: French