Senior Manager - Qualitätssicherung – Parenteral (m/w/d)

Eli Lilly UK

Alzey, Germany
Competitive salary; not specified; excellent pensi...
**
5 years leadership experience in pharmaceutical industry
Cgmp regulations and quality management systems knowledge
German and english communication skills
** Eli Lilly UK is seeking a Senior Manager for Quality Assurance in its new parenteral production facility in Alzey, Germany. The ideal candidate will have at least 5 years of experience in the pharmaceutical industry, particularly in quality assurance, with a focus on cGMP regulations, and the role involves leading a QA team to ensure high-quality standards in drug manufacturing. **

Job Summary

  • This role involves leading the operational QA organization for a new high-tech pharmaceutical production site in Alzey, Germany starting in 2027.
  • The successful candidate will support the start-up and routine operation of QA for parenteral products including formulation, aseptic filling, and visual inspection.
  • Lilly offers a competitive salary, excellent pension plan, and access to the Corporate Lilly University for professional development.

Matching Summary

Match Score: 75

** Eli Lilly UK is seeking a Senior Manager for Quality Assurance in its new parenteral production facility in Alzey, Germany. The ideal candidate will have at least 5 years of experience in the pharmaceutical industry, particularly in quality assurance, with a focus on cGMP regulations, and the role involves leading a QA team to ensure high-quality standards in drug manufacturing. **

Salary

Competitive salary; Not specified; Excellent pension plan and individual benefits

Skills & Requirements

Must-have

  • 5 years leadership experience in pharmaceutical industry
  • cGMP regulations and quality management systems knowledge
  • German and English communication skills
  • Parenteral production environment experience
  • C&Q and validation document approval

Nice-to-have

  • Experience with new plant startup or commissioning
  • Knowledge of Trackwise or Veeva systems
  • Background in aseptic process simulation
  • Strong technical writing skills in German and English
  • Experience with Manufacturing Execution Systems

Key Requirements

  • Bachelor's degree in natural sciences, engineering, or related field
  • Minimum 5 years of leadership experience in pharmaceutical QA
  • Proven understanding of cGMP regulations and data integrity
  • Fluency in both German and English required

Work Rights

Not specified

Tailored Resume

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