Head of Quality (EU-GMP Transition) – Medical Cannabis
Company: WeGROW Cannabis Lesotho
Location: Teyateyaneng, Lesotho
Reports To: Chief Executive Officer (CEO) / Managing Director
Position: Full-Time
Company Description
WeGROW Cannabis Lesotho is a premium cannabis cultivation and processing company located 1,600 meters above sea level in the mountains of Lesotho. Operating under strict CUMCS-GAP and GACP compliance, and in collaboration with an EU-GMP certified processing facility, WeGROW specializes in supplying high-quality medical cannabis for the European pharmaceutical market. The company focuses on sustainability, excellence, and production of diverse cannabis strains aligned with global patient needs — while maintaining rigorous international quality standards.
Role Description
The Head of Quality will lead the establishment and continual improvement of the Quality Management System (QMS) as the company transitions from GACP-compliant cultivation to EU-GMP certified post-harvest processing.
This role holds responsibility for regulatory compliance, product quality, batch readiness, process validation, internal audits, documentation governance, and EU-GMP inspection readiness. Oversight covers all stages of post-harvest: drying on branches, debudding, trimming, curing, and packaging.
Key Responsibilities
1. Quality Leadership & Compliance
• Lead implementation and maintenance of the EU-GMP QMS
• Ensure compliance with GACP, EU-GMP Parts I & II, and national regulations
• Act as authority for post-harvest quality (drying, debudding, trimming, curing, packaging)
• Serve as main contact for regulators, auditors, and certification bodies
2. EU-GMP Transition & Inspection Readiness
• Develop and execute the EU-GMP transition roadmap
• Lead equipment and facility qualification (URS, DQ, IQ, OQ, PQ)
• Lead validation of drying, debudding, trimming, curing, and packaging processes
• Prepare site and team for EU-GMP audits
3. Batch Release & Documentation
• Review and approve MBRs, BPRs, and traceability documentation
• Approve deviations, change controls, and CAPAs
• Ensure documentation follows ALCOA+ standards
4. Quality Control Oversight
• Manage internal and external QC testing (cannabinoids, terpenes, microbiology, pesticides, heavy metals, residual solvents, water activity)
• Maintain sampling and retain programs
• Ensure stability programs are implemented
5. Quality Assurance Systems
• Maintain SOPs, quality manuals, policies
• Implement internal audits and supplier qualification
• Ensure staff GMP training compliance and records
6. Post-Harvest Workflow Compliance
• Approve cleanroom classification, zoning, and environmental monitoring
• Approve sanitation, personnel and material flow procedures
7. Leadership & Team Development
• Build and manage the Quality Unit (QA, QC, Documentation)
• Develop quality culture throughout operations
Required Qualifications
Education
• Bachelor’s or Master’s degree in Life Sciences, Biotechnology, Chemistry, Pharmacy, Agronomy, or related field
• Advanced pharmaceutical/GMP training is an advantage
Experience
• Minimum 5+ years in GMP-regulated Quality roles (pharma, biotech, medical cannabis, food supplements)
• EU-GMP implementation or inspection preparation experience preferred
• GACP or cannabis industry exposure is an asset
Competencies
• Strong EU-GMP regulatory knowledge
• Expertise in deviations, CAPA, risk management, batch review, and audits
• Project leadership and stakeholder communication
Key Performance Indicators (KPIs)
• Successful EU-GMP certification
• Zero major audit findings
• Timely CAPA and change control closure
• Full documentation compliance (ALCOA+)
• Measurable reduction in operational quality risk
Remuneration
• Market competitive (based on experience)
How to Apply
Submit:
• Detailed CV
• Certified ID/Passport
• Certified academic transcripts
• Two reference letters (including one from most recent supervisor)
Email: [email protected]
Deadline: 08 December 2025
Late applications will not be considered.