Quality Analyst (EN/FR)

Proclinical; Neuenburg; On-site; CHF 90,000 - 120,000; Full time

Job summary

Proclinical is seeking a bilingual Quality Analyst to join our team in Switzerland. The role focuses on quality control within the pharmaceutical industry, with emphasis on cardiovascular therapy, cGMP compliance, and hands-on laboratory methods.

You will perform analyses, support continuous improvement, ensure accurate documentation (ALCOA), and collaborate with cross-functional teams. Fluency in French and English is required, along with a valid Swiss work permit.

Qualifications

• Educational background in biology, biochemistry, or a related scientific field (CFC or equivalent).
• Experience in a QC laboratory environment under cGMP standards.
• Proficiency in techniques such as electrophoresis, HPLC, ELISA, or enzymatic activity determination.
• Swiss/EU nationality or valid Swiss work permit.
• Experience in drafting method validation protocols is a plus.

Responsibilities

• Perform biochemical analyses and supervise activities per GMP/BPD rules.
• Prepare laboratory solutions for analyses.
• Adhere to all current procedures and EHS regulations.
• Accurately complete forms, logbooks, and documentation following ALCOA.
• Notify the supervisor of non-conforming or invalid results promptly and initiate quality system events within deadlines.
• Manage laboratory investigations and troubleshoot minor issues within your expertise.
• Execute protocols for reagent qualification, consumables validation, and equipment/method validation.
• Ensure calibration and maintenance of equipment during analysis.
• Maintain real-time Kanban management and report procedural deviations.
• Organize and maintain the laboratory according to 5S standardization norms.
• Support continuous improvement initiatives.

Skills

French language

English language

Education

Biology / Biochemistry degree (CFC or equivalent)

Tools

HPLC

ELISA

Electrophoresis

Enzymatic activity

Job description

Are you a bilingual Quality Analyst with a passion for laboratory excellence, regulatory compliance, and ensuring the highest standards in pharmaceutical quality control?

Proclinical is seeking a bilingual (English/French) Quality Analyst to join a dynamic team in Switzerland. This role focuses on quality control within the pharmaceutical industry, particularly in the cardiovascular therapy area. The position requires hands‑on experience with biochemical laboratory methods and a strong understanding of cGMP standards. You will play a key role in ensuring compliance, conducting analyses, and supporting continuous improvement initiatives.

Please note that to be considered for this role you must have the right to work in this location or hold an EU passport.

Responsibilities:

• Perform biochemical analyses and supervise activities in accordance with laboratory procedures and GMP/BPD rules.
• Prepare laboratory solutions for analyses.
• Adhere to all current procedures and EHS regulations.
• Accurately complete forms, logbooks, and documentation following Good Manufacturing and Documentation Practices (ALCOA).
• Notify the supervisor of non-conforming or invalid results promptly and initiate quality system events within deadlines.
• Manage laboratory investigations and troubleshoot minor issues within your expertise.
• Execute protocols for reagent qualification, consumables validation, and equipment/method validation.
• Ensure calibration and maintenance of equipment during analysis.
• Maintain real-time Kanban management and report procedural deviations.
• Organize and maintain the laboratory according to 5S standardization norms.
• Support continuous improvement initiatives.

Key Skills and Requirements:

• Educational background in biology, biochemistry, or a related scientific field (CFC or equivalent).
• Experience in a QC laboratory environment under cGMP standards.
• Proficiency in techniques such as electrophoresis, HPLC, ELISA, or enzymatic activity determination.
• Fluency in French and technical proficiency in English.
• Swiss/EU nationality or valid Swiss work permit.
• Experience in drafting method validation protocols is a plus.
  

If you are having difficulty in applying or if you have any questions, please contact Olivier Worch at [e-mail].