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eCompliance-Specialist

Quindoo - it solutions GmbH

Langkampfen

Hybrid

EUR 40 000 - 60 000

Vollzeit

Heute
Sei unter den ersten Bewerbenden

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Zusammenfassung

A leading IT solutions company in Austria is seeking an individual to support the Quality & Compliance Manager in ensuring the quality of GxP-relevant systems. Ideal candidates should have technical education, experience in quality assurance, and strong communication skills in German and English. The position offers a flexible hybrid work model and a salary starting from €3,950 gross/month.

Leistungen

Attractive salary
Flexible work arrangement
Dynamic team environment

Qualifikationen

  • Experience in the pharmaceutical field, quality assurance, or system validation is an advantage.
  • Understanding of GMP / GxP regulations (EU, FDA, etc.).
  • Structured, analytical, and solution-oriented mindset.

Aufgaben

  • Support the Quality & Compliance Manager in ensuring quality throughout the lifecycle of systems.
  • Contribute to validation activities, change control, and risk assessments.
  • Perform QA reviews and document approvals.

Kenntnisse

Attention to detail
Teamwork
Analytical mindset
Communication skills in German
Communication skills in English

Ausbildung

Technical, scientific, or IT education

Tools

Common Office applications
IT applications
Jobbeschreibung

Are you passionate about quality and smart processes? Bring your energy, take responsibility, and join our team in eCompliance & quality.

Your Mission:
  • Support our Quality & Compliance Manager in ensuring the quality of GxP‑relevant computer systems throughout their entire lifecycle – from implementation to ongoing operation (laboratory, production, and IT systems)
  • Contribute to validation activities, change control, deviation management, CAPA, and risk assessments
  • Perform QA reviews and document approvals Support audits, inspections, and data integrity initiatives
  • Advise teams on establishing simple, secure, and compliant processes
  • Actively contribute to the continuous improvement of our quality processes and standards
What You Bring:
  • Completed technical, scientific, or IT education
  • Experience in the pharmaceutical field, quality assurance, or system validation is an advantage
  • Understanding of GMP / GxP regulations (EU, FDA, etc.)
  • Structured, analytical, and solution-oriented mindset with high attention to detail and strong teamwork skills
  • Confident in using common Office and IT applications
  • Excellent German and English communication skills, with the ability to explain complex topics clearly and appropriately for different audiences
Why Join Quindoo?
  • Meaningful work: You ensure that systems are safe, reliable, and audit-ready
  • Flexible: Hybrid work, modern tools, autonomous tasks – part‑time possible
  • Team spirit: Open, supportive, and dynamic – we learn from each other
  • Fair: Attractive salary, benefits, and transparent development opportunities

Sounds like you? Send us your CV – let’s talk!

Salary: Starting from €3,950 gross/month (IT Collective Agreement, ST2) — higher pay possible depending on qualifications and experience.

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