GLP Auditor

Das ist der Job

Position Summary We are seeking a quality-oriented GLP Auditor / Data Reviewer (m/f/d).

Darum lohnt es sich

Adryan is an internationally operating services group with offices in The Netherlands and Switzerland. Our teams work with top clients in the life sciences sector, ensuring the highest quality and commitment.

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 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.

We specialize in providing a full range of services for the life sciences industry, focusing on Project Management, Technical Operations, CQV, and Compliance. 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.

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.

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 #J-18808-Ljbffr