Evening Quality Technician I (GMP/Lean)

Curio Wellness; Towson (MD); On-site; USD 29,000 - 32,000; Part time

Job summary

Curio Wellness is seeking a Quality Technician I for a part-time evening shift in Towson, MD (Mon-Fri 5:15 PM - 10:15 PM). The role focuses on driving in-process quality within Cultivation and Manufacturing areas and reports to the Site Quality Manager.

Responsibilities include ensuring cGMP/cGAP adherence, participating in audits, root-cause analysis, approving standard work for production cells, inspecting materials and products, and supporting Lean improvements and sanitation practices.

Qualifications

• High School Diploma or GED; or 1+ year of quality experience; or equivalent combination of education and experience.
• Lean mindset with ownership.
• Experience in GMP/regulated manufacturing environments.
• Strong written and verbal communication; ability to follow written procedures.

Responsibilities

• Ensure cGMP or cGAP standards per state regulations are adhered to.
• Collaborate with internal and external audits.
• Participate in root cause analysis for quality outages.
• Approve standard work for cells prior to production, including ATP swabbing.
• Execute daily tasks, projects and objectives.
• Inspect materials and finished products for quality.
• Maintain professionalism and service culture.
• Ensure daily policy compliance including HR, security, dress code and schedules.
• Input to Lean process improvements for manufacturing quality programs.
• Oversee sanitation practices and disposal of non-conforming material.

Skills

Lean

GMP experience

Critical thinking

Written and verbal communication

Procedural adherence

Self-motivated

Analytical/data interpretation

Attention to detail

Computer/office proficiency

ServSafe certification

Responsible Vendor Training

Education

High School Diploma or GED

Job description

Curio Wellness is seeking a Quality Technician I for a part-time evening shift in Towson, MD (Mon-Fri 5:15 PM - 10:15 PM). The role focuses on driving in-process quality within Cultivation and Manufacturing areas and reports to the Site Quality Manager.

Responsibilities include ensuring cGMP/cGAP adherence, participating in audits, root-cause analysis, approving standard work for production cells, inspecting materials and products, and supporting Lean improvements and sanitation practices.