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GLP Auditor

Job in 4040, Basel, Kanton Basel-Landschaft, Switzerland
Listing for: Adryan
Full Time position
Listed on 2026-07-07
Job specializations:
  • Quality Assurance - QA/QC
  • Healthcare
Salary/Wage Range or Industry Benchmark: 80000 - 100000 CHF Yearly CHF 80000.00 100000.00 YEAR
Job Description & How to Apply Below

Adryan is an internationally operating services group with offices in The Netherlands and Switzerland. We specialize in providing a full range of services for the life sciences industry, focusing on Project Management, Technical Operations, CQV, and Compliance. Our teams work with top clients in the life sciences sector, ensuring the highest quality and commitment.

Position Summary

We are seeking a quality-oriented GLP Auditor / Data Reviewer (m/f/d). In this role, you will be responsible for reviewing and verifying scientific raw data and paper-based study documentation in accordance with Good Laboratory Practice (GLP).

This role serves as a central interface between the operational laboratory and study departments and Quality Assurance. You will ensure that all data is documented in a complete, consistent, traceable, and regulatory-compliant manner before it is incorporated into reports and regulatory submissions.

Main Responsibilities
  • Reviewing paper-based study documentation, raw data, laboratory records, and related documents for completeness, consistency, and GLP compliance
  • Reconciling data from internal databases with the corresponding original documents (paper records)
  • Identifying, documenting, and tracking deviations, discrepancies, or missing information
  • Conducting data reviews in accordance with internal QA processes and GLP requirements
  • Assisting with internal audits and inspections
  • Creating and maintaining audit trail documentation, review reports, and quality records
  • Working closely with study directors, scientists, and operational teams to resolve data-related issues
Requirements
  • Experience on Swiss Ordinance on Good Laboratory Practice of 18 May 2005 and the relevant OECD GLP guidelines
  • QC/QA experience is also considered
  • Demonstrated proficiency in GLP audit procedures and documentation.
  • Knowledge of routine analytical methodologies, with an emphasis on chromatography
  • Knowledge of computerized system validation
  • Good interpersonal skills with demonstrable tact and diplomacy
  • Good computer skills including Microsoft Word and Excel. Knowledge of MS-Access and SQL would be a plus
  • With your openness and understanding of mutuality, your active communication and continuous value assessment you foster and encourage our team mentality. You communicate and work effectively with scientific staff at all levels within the Testing Facility and you see yourself as a creative problem solver.
  • Good oral and written communication skills in German and English
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