Junior Computer System Validation Consultant - Life Science

PQE Group; Germany (OH); On-site; USD 51,813 - 63,327; Full time

Job summary

PQE Group is seeking a Junior Computer System Validation (CSV) Consultant to support projects across Germany, Austria and Switzerland. The role requires travel within the DACH area and on-site activity.

You will assist in validation activities, develop IQ/OQ/PQ protocols, and ensure GMP/GxP/SOP compliance while producing lifecycle documentation. A Life Sciences degree plus German fluency and English proficiency are preferred.

Qualifications

• Bachelor's or Master’s degree in a technical-scientific field (Life Sciences preferred).
• Fluent in German and strong English skills (B2+).
• Willingness to travel within the DACH region.

Responsibilities

• Assist in validation, verification, and qualification of equipment and systems.
• Develop and execute IQ/OQ/PQ testing protocols.
• Ensure compliance with GMP/GLP/GCP/QSR and SOPs.
• Prepare project documentation and lifecycle reports.
• Maintain traceability of documents and proper storage.
• Work under supervision of project leaders and meet timelines.

Skills

English (B2)

German (Fluent)

Curiosity/Proactivity

Education

Life Sciences degree

Job description

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 Germany, Austria and Switzerland.

The ideal candidate is comfortable to travel in DACH-Area, depending on the project phase and

on-site activity needs.

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
• Salary starts from 50.000€ gross per year

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.