Specialist (m/w/d) Qa Audit Management

Simtra BioPharma Solutions

Halle, Germany
Tariff-based compensation; includes 13th salary + ...
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Gmp knowledge and application
Customer audit management
Trackwise global audit module
** Simtra BioPharma Solutions is seeking a Specialist (m/w/d) for QA Audit Management at their Halle, Germany location. The role involves managing customer audits and regulatory inspections, requiring a background in chemistry, pharmacy, or biology, along with experience in the pharmaceutical environment. **

Job Summary

  • The role ensures the smooth operation of customer audits and regulatory inspections at the Halle/Westfalen facility.
  • Candidates will manage the complete lifecycle of audits including preparation, execution, follow-up, and data entry in TrackWise.
  • The company offers a comprehensive benefits package including 30 days of vacation, a 13th salary, and free parking.

Matching Summary

Match Score: 75

** Simtra BioPharma Solutions is seeking a Specialist (m/w/d) for QA Audit Management at their Halle, Germany location. The role involves managing customer audits and regulatory inspections, requiring a background in chemistry, pharmacy, or biology, along with experience in the pharmaceutical environment. **

Salary

Tariff-based compensation; Includes 13th salary and vacation pay; Benefits: Company pension, care insurance, subsidized canteen

Skills & Requirements

Must-have

  • GMP knowledge and application
  • Customer audit management
  • TrackWise global audit module
  • Fluent German and English communication

Nice-to-have

  • Aseptic or sterile manufacturing experience
  • Third party audit execution
  • Diplomatic communication skills
  • Structured and responsible work style

Key Requirements

  • Degree in Chemistry, Pharmacy, or Biology
  • Approximately 2 years of pharmaceutical industry experience
  • Strong understanding of GMP guidelines

Work Rights

Not specified

Tailored Resume

Cover Letter