Onsite Consultant GMP Compliance, Quality Assurance

Posted 2 days ago

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About the role

  • Consultant for GMP compliance and quality assurance in Life Sciences. Engage in validation projects and assist in compliance documentation.

Responsibilities

  • Participation in the development of optimized qualification and validation concepts
  • Performing qualifications of high‑tech equipment and systems in the pharmaceutical and biopharmaceutical industry
  • Participation in risk analyses
  • Support in validation projects (e.g., cleaning, process and method validations)
  • Preparation of GMP‑compliant documentation, including Standard Operating Procedures (SOPs)
  • Review of technical documents and drawings, as well as changes and deviations

Requirements

  • Degree in Process Engineering, Pharmaceutical Engineering, Biotechnology, Chemical Engineering, Life Sciences Engineering, or a comparable engineering or natural sciences degree
  • Strong technical understanding and the ability to quickly familiarize yourself with different areas of responsibility
  • Experience in a GMP environment is an advantage
  • Independent and solution‑oriented working style
  • Willingness to travel for on‑site qualification activities; valid driving licence (Class B) required
  • Very good German and good English language skills

Benefits

  • Exciting and varied projects
  • A collegial team and an assigned mentor
  • Flexible location and working‑time model, and permanent employment contracts
  • Internal and external training and development opportunities
  • Open company culture with short decision‑making paths

Job title

Consultant GMP Compliance, Quality Assurance

Job type

Experience level

Mid levelSenior

Salary

Not specified

Degree requirement

Bachelor's Degree

Location requirements

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