Onsite Principal Consultant – Pharmaceutical Quality Assurance / GMP

Posted 4 hours ago

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About the role

  • Principal Consultant focusing on GMP compliance consulting within the pharmaceutical industry. Working with a team on various quality assurance projects worldwide.

Responsibilities

  • General GMP compliance and strategic consulting
  • Preparation for and support during regulatory inspections
  • Conducting audits, gap analyses, and due diligence studies
  • Advising on supply chain strategies (MAH (Marketing Authorisation Holder), MAA (Marketing Authorisation Application) topics)
  • Delivering training, mentoring, and workshops
  • Contributing to the development of internal tools and work materials
  • Active participation in industry association activities, presentations, and technical publications
  • Business development and ongoing client relationship management in consulting projects

Requirements

  • Completed degree in a scientific or technical field, ideally with a PhD
  • At least 10 years of professional experience in GMP compliance consulting
  • 2–3 years of relevant hands-on experience on the manufacturer side
  • Excellent German and English skills, both written and spoken
  • Strong consulting skills and solid technical expertise
  • Willingness to travel for project assignments

Benefits

  • Flexible working hours and location model
  • 30 days holiday
  • Permanent employment contract
  • Open corporate culture with flat hierarchies
  • Attractive benefits package
  • Company car
  • Additional perks

Job title

Principal Consultant – Pharmaceutical Quality Assurance / GMP

Job type

Experience level

Lead

Salary

Not specified

Degree requirement

Postgraduate Degree

Location requirements

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