Quality Control Analyst m/f/d

Aristo Group; Neuenburg; Presencial; CHF 90.000 - 120.000; Jornada completa

Descripción de la vacante

Aristo Group is seeking a QC Analyst to join its quality control laboratory. You will carry out biochemical analyses and supervisory tasks according to laboratory procedures and cGMP/GDP requirements.

The work is in a close, relaxed team where tasks change quickly, so you will need to stay motivated in a fast-moving environment while delivering high-quality results. The role is payroll-based with tasks spanning validation, documentation, and investigations to ensure GMP compliance and continuous

Formación

• 3+ years in a QC lab within a cGMP pharmaceutical environment.
• Experience with electrophoresis, HPLC, ELISA, or enzyme activity assays.
• Structured, quality-focused way of working with routine tasks.
• Fluent French and technical English.

Responsabilidades

• Perform biochemical analyses (ELISA, PCR, HPLC, Western Blot, enzyme activity assays) according to SOPs and GMP/GDP rules
• Prepare solutions used in laboratory analyses
• Document results in forms, logbooks, and records following GMP and ALCOA+ principles
• Report non-conforming or invalid results to your supervisor the same day and initiate quality events in the quality system on time
• Support laboratory investigations and continuous improvement initiatives
• Execute qualification protocols for reagents and consumables, and validation protocols for methods, systems, and equipment
• Ensure calibration and maintenance of equipment are up to date before analysis
• Manage Kanban and planning requests in real time, and upscale issues proactively
• Maintain the laboratory in line with 5S standards and comply with EHS rules

Conocimientos

microbiology

ELISA

HPLC

French

Educación

EFZ Laborant/in / Lab technician qualification

Biology or related science

Herramientas

Electrophoresis

HPLC equipment

ELISA kits

Descripción del empleo

Our client is looking for a QC Analyst to join its quality control laboratory. You will carry out biochemical analyses and supervisory tasks according to laboratory procedures and cGMP/GDP requirements. The work takes place in a close, relaxed team where tasks change quickly, so you will need to stay motivated in a fast-moving environment while delivering high-quality results.

Type of employment: Payroll

Skills: microbiology, ELISA, HPLC, French

Project start: ASAP

Tasks:

• Perform biochemical analyses (e.g. ELISA, PCR, HPLC, Western Blot, enzyme activity assays) according to SOPs and GMP/GDP rules
• Prepare solutions used in laboratory analyses
• Document results in forms, logbooks, and records following GMP and ALCOA+ principles
• Report non-conforming or invalid results to your supervisor the same day and initiate quality events in the quality system on time
• Support laboratory investigations and continuous improvement initiatives
• Execute qualification protocols for reagents and consumables, and validation protocols for methods, systems, and equipment
• Ensure calibration and maintenance of equipment are up to date before analysis
• Manage Kanban and planning requests in real time, and upscale issues proactively
• Maintain the laboratory in line with 5S standards and comply with EHS rules

Qualifications:

• Vocational training as a laboratory technician (EFZ Laborant/in), biology, or another relevant scientific field
• At least 3 years of experience in a QC laboratory in a cGMP environment (pharmaceutical industry)
• Practical experience with electrophoresis, HPLC, ELISA, or enzyme activity determination
• Experience writing method validation protocols is an advantage
• Structured, quality-focused way of working, with motivation for routine tasks
• Fluent French and technical English
• Swiss or EU citizenship, or a valid Swiss work permit