Expert in GLP-QA

SEC Life Sciences; Düsseldorf; Hybrid; EUR 35.000 - 55.000; Teilzeit

Zusammenfassung

A leading organization in life sciences is seeking a part-time GLP Quality Assurance Expert. This contract role involves ensuring compliance and data integrity in preclinical studies, with flexible working arrangements and a defined project timeline. The ideal candidate has a strong GLP background and experience in quality assurance processes.

Qualifikationen

• Proven track record in Good Laboratory Practice (GLP) within a scientific or regulatory setting.
• Strong familiarity with preclinical study workflows.
• Direct experience reviewing regulatory documentation, ideally involving human tissue studies.

Aufgaben

• Conduct independent audits to ensure alignment with GLP principles.
• Review, amend, and approve study plans and documents.
• Provide real-time input on quality standards during preclinical research.

Kenntnisse

Quality Assurance

Regulatory Compliance

Attention to Detail

Jobbeschreibung

Contract GLP Quality Assurance Expert (m/f/d)
Part-time | Hybrid (Munich-based) | Contract until Dec 2025

A leading organisation in the life sciences sector is seeking a GLP Quality Assurance Expert to support ongoing preclinical study work. With a focus on regulatory compliance and data integrity, this contract position plays a critical role in the preparation and review of study documentation for submission. The project has a clear timeline, offering flexibility outside of peak periods, with heavier involvement required from August through October 2025.

This is an ideal opportunity for someone with a strong GLP background, proven experience in quality assurance processes, and a detail-oriented approach to documentation and regulatory standards.

Your role as GLP Quality Assurance Expert:

• Conduct independent audits of scientific studies to ensure alignment with GLP principles and regulatory expectations
• Review, amend, and approve study plans, deviations, and final reports for structure, consistency, and compliance
• Assess raw data and documentation to confirm accuracy, integrity, and adherence to protocols
• Provide real-time input on quality standards during the execution of preclinical research
• Support internal stakeholders with expert guidance on GLP best practices and quality-related queries
• Ensure all study outputs meet the necessary standards for submission, including completeness and traceability

Experience and qualifications for the GLP Quality Assurance Expert role:

• Proven track record in Good Laboratory Practice (GLP) and Quality Assurance within a scientific or regulatory setting
• Hands-on laboratory background, with strong familiarity with preclinical study workflows
• Direct experience reviewing regulatory documentation, ideally involving human tissue studies
• High attention to detail and comfort working independently to tight deadlines
• Availability to be on-site in Munich on short notice during peak study phases (August-September)
• Able to commit to 15-30 hours per week as needed through to project completion

This is a contract-based opportunity offering flexible working arrangements, a defined project timeline, and the chance to contribute to critical regulatory deliverables in a high-impact area of life sciences.

For immediate consideration, apply today. Alternatively, reach out directly to learn about similar contract opportunities in GLP and quality assurance

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