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Junior QC Analyst (M/F/D)
Tasks:
Perform and approve analytical results in the QC laboratory according to SOPs, cGMP, and applicable standards.
Ensure compliance with Good Documentation Practices and accurately complete forms, logbooks, and electronic systems.
Identify and report non-conforming or invalid results immediately, initiating quality system events as required.
Execute reagent/consumable qualifications, method, system, and equipment validation protocols.
Maintain laboratory organization, adhere to 5S standards, and ensure proper equipment calibration and maintenance.
Support continuous improvement initiatives, GEMBAs, HOP, and troubleshooting of minor issues.
Train analysts on equipment and procedures, acting as a backup GMP trainer when needed.
Manage and review equipment logbooks, and support vendor maintenance or unplanned interventions.
Participate in deviation management, risk analyses, trend reports, and inspections/audits.
Act as subject matter expert (SME) for projects, regulatory submissions, and corrective/preventive actions.
Qualification:
Minimum CFC in microbiology or equivalent experience in the pharmaceutical/biotech industry.
2–5 years of experience in a cGMP laboratory or at least 2 years as Analyst I.
Minimum 5 years in a cGMP laboratory or 5 years as Analyst II.
Good to very good knowledge of laboratory methods.
Good knowledge of cGMP.
Knowledge of Data Integrity principles, with advanced knowledge preferred.
Proficient in standard IT tools (MS Office).
Fluent in French and English (technical).
English level B2 minimum.
Requirements:
Start: 22.09.2025
Duration: 5 months
Capacity: 5 days per week
Location: Neuchatel, Switzerland
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