Pure Holding AG
Zeiningen
15 hours ago
Quality Manager Pharma and Deputy Qualified Person (m/f/d)
- 02 April 2026
- 100%
- Permanent position
- Zeiningen
About the job
Do you want to take on a responsible role in one of Europe’s most dynamic new industries? Then become part of our team and help shape the future of cannabis with us.
Pure Holding AG is one of the leading corporate groups in the Swiss cannabis industry and has developed since its founding into an integrated provider along the entire cannabis value chain – from research and genetics through production to consumer and medical products. As the parent organization of several specialized subsidiaries, it forms the strategic backbone of the group.
Among our most important companies, besides Pure Production AG, one of the leading providers in the Swiss cannabis recreational market, is Puregene AG, an internationally active plant technology company with an advanced breeding program based on biochemistry, bioinformatics, and genomics. Furthermore, Pure Pharma AG, which specializes in the cannabis pharmaceutical market, complements the group. GreenLee AG, through which the Pure Group is also successfully positioned in the cannabis wholesale sector, further strengthens us. Together, these companies form one of the few cannabis groups in Europe that covers the entire value chain from genetics to the end product.
As Quality Manager Pharma and Deputy Qualified Person (m/f/d), you will take on a central role in building and further developing our quality and compliance structures and ensure that our products and processes meet the highest regulatory and quality requirements.
Quality Manager Pharma and Deputy Qualified Person (m/f/d)
Your responsibilities:
- Operational management, monitoring, and further development of the quality management system
- Deputizing the Qualified Person in the operational context
- Close coordination with the Qualified Person in relevant decision-making processes
- Evaluation and approval of quality processes in daily business
- Ensuring the functionality of narcotics-relevant systems (e.g., MESA, JARE, NDS) as well as checking the narcotics balance
- Preparation and review of regulatory notifications for release by the Qualified Person
- Operational responsibility for audits and inspections
- Coordination of authority communication in coordination with the Qualified Person
- Management reporting as well as evaluation of quality indicators and trends
Your profile:
- Technical, scientific, or pharmaceutical basic training, or studies with further training in the GMP area
- Several years of experience in quality management in the pharmaceutical environment
- Solid GxP knowledge
- Solution-oriented approach, strong communication skills
- High commitment as well as goal- and performance-oriented working style
- Entrepreneurial and communicative personality with strong self-motivation
- Impeccable reputation
- Very good German and English skills, spoken and written
- Confident handling of MS Office
Our offer:
At Pure, people work who want to take responsibility and explore new paths. Our corporate culture is characterized by:
- Pioneering spirit – We operate in a young industry and actively shape its development.
- High quality standards – Quality, compliance, and transparent processes are central components of our work.
- Personal responsibility and scope for design – Short decision-making paths enable taking responsibility and implementing ideas.
- Interdisciplinary collaboration – Research, production, quality, and market work closely together with us.
- Pragmatic entrepreneurship – We are a dynamic company and continuously develop ourselves.