Quality Assurance Specialist Pharma (m/f/d) 60-100%
Laufenburg
Key information
- Publication date:12 November 2025
- Workload:60 – 100%
- Contract type:Permanent position
- Place of work:Laufenburg
Job summary
Pure Holding AG leads the Swiss cannabis industry, comprising six subsidiaries. Join us to shape the future of medical cannabis!
Tasks
- Ensure products meet high quality and compliance standards.
- Support development of quality management systems per GMP/GDP.
- Assist with audits, inspections, and supplier qualifications.
Skills
- Technical or pharmaceutical education with GMP experience required.
- Strong knowledge of GMP, GDP, and GACP standards.
- Excellent communication and teamwork skills essential.
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Pure Holding AG is the market leader in the Swiss cannabis industry and consists of six subsidiaries covering different areas of the cannabis value chain. Pure Pharma AG, a part of Pure Holding AG based in Laufenburg, focuses on the distribution of medical cannabis products. With a consistent quality standard and a deep understanding of regulatory requirements, Pure Pharma contributes to establishing medical cannabis. To actively shape this exciting growth phase, we are looking for a committed individual to help us shape the future of medical cannabis.
Quality Assurance Specialist Pharma (m/f/d) 60-100%
Your responsibilities:
As a member of our quality management team, you report directly to the Quality Manager and ensure that our products meet the highest quality and compliance requirements.
- Participation in the establishment, maintenance, and further development of the quality management system according to GMP/GDP/GACP
- Creation, revision, and approval of quality-relevant documents (SOPs, work instructions, forms)
- Support in handling deviations, CAPA, and change control processes
- Preparation, accompaniment, and follow-up of internal and external audits as well as regulatory inspections
- Collaboration in supplier qualifications and document reviews
- Support in GMP training for employees
- Documentation and follow-up of hygiene, safety, and training measures
- Participation in batch release and implementation of regulatory requirements
- Ensuring compliance with internal guidelines and legal quality standards
Your profile:
- Completed technical or pharmaceutical basic training (e.g., laboratory technician, pharmaceutical technologist, druggist, or comparable)
- Initial professional experience or further training in the GMP/GDP environment
- Good knowledge of GMP, GDP, ideally also GACP
- Structured, solution-oriented, and responsible working style
- Enjoyment of teamwork, communication, and process optimization
- Very good German skills in spoken and written form, good English skills; additional languages are an advantage
- High independence, initiative, and flexibility with changing priorities
- Willingness to participate in additional areas of responsibility as needed
Our offer:
- Varied, responsible activity in an international, innovative company
- High personal responsibility and scope for design
- Collegial, motivated team with a hands-on mentality
- 5 weeks of vacation, permanent employment contract, 100% continued salary payment during maternity/paternity leave, accident supplementary insurance
- Opportunity to contribute your own ideas and actively contribute to the company's success
- Work in a future-oriented market segment with clear growth prospects
- Short decision-making paths and a dynamic environment
- Flexible working hours for individual needs
- Very good development opportunities and self-organized work