Produktionsassistent GMP Produktion (m/w/d)
MedropharmKradolf-Schönenberg, Thurgau, Switzerland
Posted March 3, 2026
Full Time
About the Company
Medropharm is a Swiss-based company specializing in the extraction, manufacturing, and commercialization of pharmaceutical-grade cannabinoids and plant-derived products. Leveraging advanced extraction technologies and stringent quality controls, the firm develops high-potency cannabis medicines and cannabidiol (CBD) formulations for therapeutic use. Its portfolio spans prescription-grade treatments, over-the-counter CBD supplements, and research-grade health science products, positioning Medropharm as a trusted partner for clinicians and researchers worldwide. The company's commitment to scientific rigor, regulatory compliance, and sustainable sourcing distinguishes it in the rapidly evolving cannabinoid market.
Job Description
The Production Assistant (m/w/d) is responsible for the proper execution of assigned tasks within the GMP-classified production areas of Medropharm AG, following EU-GMP guidelines, internal quality specifications, and applicable narcotics regulations.
Requirements
- Execution of all work according to released standard operating procedures (SOPs), manufacturing instructions, and valid reference documents
- Consistent adherence to clothing, hygiene, and contamination control specifications
- Ensuring order and cleanliness in the production area in accordance with EU-GMP requirements
- Responsible handling of materials and production resources
- Acceptance, unpacking, and internal provision of cannabis flowers in accordance with applicable work and safety instructions
- Execution of manual or semi-manual trimming work
- Packaging and repackaging of narcotics under controlled GMP conditions
- Labeling of primary and secondary packaging according to batch documentation
- Inspection of material identity, batch numbers, and labelling specifications before further processing
- Close cooperation with Quality Assurance (QA) in handling deviations, inconsistencies, or quality defects
- Execution of cleaning work on premises, equipment, and tools according to validated cleaning procedures
- Documentation of all cleaning activities according to the principles of good documentation practice (GDP)
- Support for Line-Clearance measures before and after production campaigns
- Proper and prescribed handling of cleaning agents according to SOP
- Timely, complete, and traceable documentation of all activities in manufacturing protocols, logbooks, and forms in accordance with the ALCOA principles
- Ensuring compliance with the principles of good documentation practice (GDP)
- Contribution to material and quantity controls (reconciliation)
- Support for deviation investigations and CAPA measures as prescribed
- Disciplined work in a highly regulated GMP and narcotics environment
- Compliance with access regulations to secure production and storage areas
- Support for inventory controls and secure material handling
- Consistent adherence to all specifications for occupational safety and health
