Junior Computer System Validation Consultant - Life Science

PQE Group; Schweiz; Vor Ort; EUR 64.000 - 97.000; Vollzeit

Zusammenfassung

PQE Group in Switzerland is seeking a Junior Computer System Validation (CSV) Consultant to support projects in Switzerland, with possible assignments in Germany and Austria. You will assist in validation, verification and qualification activities for equipment and systems, and help develop testing protocols (IQ/OQ/PQ) while ensuring GMP/GLP/GCP/QSR compliance.

Travel within the DACH region is expected. The role requires a technical-scientific degree, fluent German, strong English, and a

Qualifikationen

• Bachelor's or Master's degree in a technical-scientific discipline (preferably Life Sciences).
• Fluent German and good knowledge of English (minimum B2).
• Willingness to travel in the DACH region.

Aufgaben

• Assist in validation, verification, and qualification processes for equipment and systems.
• Develop and execute testing protocols including IQ, OQ, and PQ.
• Ensure compliance with GMP, GLP, GCP, and QSR and with SOPs.

Kenntnisse

German language

English language

Willingness to travel

Ausbildung

Bachelor's or Master's degree in Life Sciences

Jobbeschreibung

Are you ready to join a world leader in the exciting and dynamic fields of the Pharmaceutical and Medical Device industries? PQE Group has been at the forefront of these industries since 1998, with 40 subsidiaries and more than 2000 employees in Europe, Asia and the Americas.

Following a new opportunity, we are currently looking for a Junior Computer System Validation (CSV) Consultant to support our projects in Switzerland (possible also in Germany and Austria).

You will be responsible for:

• Assist in validation, verification, and, when appropriate, qualification processes for equipment and systems.
• Participate in the development and execution of testing protocols, including Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ).
• Demonstrate adherence to pharmaceutical industry standards by applying a foundational understanding of regulatory requirements such as GMP, GLP, GCP, and QSR.
• Ensure all activities comply with applicable Standard Operating Procedures (SOPs).
• Prepare project and system lifecycle documentation and reports.
• Maintain traceability of documents and ensure proper storage according to company policies.
• Efficiently execute assigned project tasks under the direct supervision of project leaders.
• Adhere to project timelines and quality standards while maintaining attention to detail

About you:

• A Bachelor's or Master's degree in a technical-scientific discipline (preferably Life Sciences)
• Good knowledge of English (minimum B2 level)
• Fluent in German
• Curiosity, initiative, and a proactive mindset
• Willingness to travel in DACH
• Nice to have: previous experience or basic knowledge in Validation
• Located in Switzerland

Working at PQE Group

As a member of the PQE team, you will be part of a challenging, multicultural company that values collaboration and innovation. PQE Group gives you the opportunity to work on international projects, improve your skills and interact with colleagues from all corners of the world.

If you are looking for a rewarding and exciting career, PQE Group is the perfect place for you.