Qualified Person (QP) – Senior Consultant, Pharma & Cannabis

This is a fully remote position, open to applicants in Germany.

📋 Description

• You will take on the responsibility as Qualified Person in accordance with §15 AMG, ensuring the proper manufacturing and release of medical cannabis.

• You will act as the Responsible Person according to MedCanG, guaranteeing compliance with all relevant regulatory requirements.

• You will provide pragmatic and solution-oriented advice to national and international clients regarding GMP, GDP, and regulatory matters.

• You will serve as the central point of contact for authorities, accompanying inspections and audits.

• You will conduct training sessions for clients and internal teams, clearly and practically conveying regulatory requirements.

• You will assist in establishing, further developing, and optimizing quality management systems.

• You will collaborate closely with internal and external stakeholders, ensuring clear and efficient communication.

⛳️ Requirements

• Qualification as a Qualified Person in accordance with §15 AMG or the formal prerequisites for it.

• Completed university degree in pharmacy, chemistry, biology, or a related field.

• Several years of professional experience in the pharmaceutical industry, ideally in quality assurance, production, or quality control.

• Solid and practical knowledge of EU-GMP regulations.

• Experience in dealing with authorities and accompanying inspections or audits.

• High decision-making security and sense of responsibility in a regulated environment (especially in the context of approvals).

• Structured, independent working style in a remote setup.

• Fluent German and English language skills, both written and spoken.

• Residence and permanent work permit in Germany.

• Willingness to undertake occasional business trips (within Germany and internationally).

• Willingness to accurately track project-specific working hours.

🏝️ Benefits

• 100% remote work within Germany – no office, no attendance requirement.

• Flexible working hours without fixed core times.

• High level of responsibility in shaping your daily work routine.

• Challenging QP responsibilities without traditional corporate structures.

• Focus on technical work – no acquisition or sales obligations.

• Stable workload from existing client projects.

• Permanent position with predictable income (no freelancer risks).

• Opportunity to actively shape quality standards and processes.

• Variety through collaboration with different companies.

• Work in a growing, regulatory demanding market (focus: medical cannabis).

• Flexible starting date – also possible at short notice.

• Lean structures and short decision-making paths.

• 30 days of vacation with flexible usage.

• No systematic overtime expected.

• Option for performance-based profit-sharing with corresponding development.

• High decision-making scope within your professional responsibilities.

• Collaboration on an equal footing without traditional hierarchies or micromanagement.