About the role

  • Quality Manager ensuring compliant clinical trial processes at TFS HealthScience. Advising on quality and compliance requirements and conducting audits and inspections.

Responsibilities

  • Advise project teams and internal functions on quality and compliance requirements, including applicable GxP standards, international guidelines, and regulatory expectations
  • Plan, coordinate, and support internal and external audits and inspections, including preparation, execution, documentation, and follow-up of findings
  • Conduct risk analyses across processes and studies, assess quality and compliance risks, and derive appropriate improvement measures
  • Support CAPA management activities, including root cause analysis, definition of corrective and preventive actions, and effectiveness checks
  • Develop and deliver targeted quality training and support the creation, maintenance, and review of SOPs, work instructions, and other quality-relevant documentation

Requirements

  • Scientific or medical degree, or comparable background, combined with several years of experience in quality management within clinical research or life sciences
  • Strong understanding of regulatory and quality requirements in clinical research, including GxP principles and end-to-end research processes
  • Experience with audits, inspections, risk management, and CAPA processes, with the ability to identify process dependencies and improvement opportunities
  • Fluent German and English language skills, both written and spoken, with willingness to travel nationally and internationally as needed

Benefits

  • Opportunities for personal and professional growth in a rewarding environment
  • Team that values collaboration, quality, and making a difference in the lives of patients

Job title

Quality Manager

Job type

Experience level

Mid levelSenior

Salary

Not specified

Degree requirement

Bachelor's Degree

Location requirements

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