QA Manager

SLS Services Limited

Dortmund

Vor Ort

EUR 45.000 - 60.000

Vollzeit

Vor 7 Tagen
Sei unter den ersten Bewerbenden
Bewerbungsgenerator

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Zusammenfassung

SLS Services Limited in Dortmund is seeking a central QA professional to ensure GMP-compliant quality management and continuous improvement across core processes. You will maintain the QMS, oversee documentation, and support audits and CAPA activities.

The role requires a degree in pharmacy or natural sciences (or equivalent vocational training with 3+ years in a regulated pharma environment), plus fluent German and English and strong computer skills. Onsite position.

Qualifikationen

  • Degree in pharmacy or natural sciences, or vocational training with 3+ years in a regulated pharmaceutical environment
  • Strong understanding of quality management under GMP conditions
  • Very good command of German and English, and confident with computer systems

Aufgaben

  • Maintain and improve the quality management system
  • Prepare, review, and oversee QM documentation
  • Manage deviations, changes, and CAPA processes
  • Plan and monitor training, qualification, and validation activities
  • Review analytical tests and support customer/regulatory audits and self-inspections

Kenntnisse

GMP knowledge
Process-oriented
Audits & compliance

Ausbildung

Bachelor degree in Pharmacy or Natural Sciences
Vocational training with 3+ years in regulated pharma

Tools

Quality Management Systems

Jobbeschreibung

With approximately 175 employees worldwide, this organisation offers a modern and supportive working culture, continuous development opportunities, and a strong focus on employee well-being. Regular team events, advanced development programs, and a collegial environment make this a fantastic place to build long-term success. This role is fully onsite.
Responsibilities / Role
In this central QA role, you will ensure compliance and continuous improvement across key processes:
  • Maintain and improve the quality management system
  • Prepare, review, and oversee QM documentation
  • Manage deviations, changes, and CAPA processes
  • Plan and monitor training, qualification, and validation activities
  • Review analytical tests and support customer/regulatory audits and self-inspections
Qualifications & Experience
  • Degree in pharmacy or natural sciences, or vocational training with 3+ years in a regulated pharmaceutical environment
  • Strong understanding of quality management under GMP conditions
  • Very good command of German and English, and confident with computer systems
Additional Skills
  • Comprehensive GMP knowledge
  • Strong process-oriented approach and problem-solving abilities
  • Ability to manage audits and compliance activities effectively
Benefits (where relevant)
  • Experience with electronic Quality Management Systems
  • Background in pharmaceutical production or analytical testing
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