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
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