Quality Assurance Specialist

Vireo Health•Palatka, FL

3d•Onsite

About The Position

The Quality Assurance (QA) Specialist serves as a critical guardian of organizational integrity, operational excellence, and regulatory compliance within the Medical Marijuana Treatment Center (MMTC) ecosystem. This role is pivotal in safeguarding product safety, brand reputation, and operational continuity. By spearheading quality oversight, driving rigorous adherence to GMP standards, and championing a culture of continuous improvement, the QA Specialist ensures that all cultivation, processing, and distribution workflows meet or exceed state statutes and industry benchmarks.

Requirements

HS Diploma; foundational understanding of compliance; high aptitude for process adherence. (Level I)
2+ years of QA experience in a regulated (GMP) environment. Proven ability to manage documentation and audit trails. (Level II)
3-5+ years of QA experience in Cannabis/Regulated Manufacturing. GMP Certified. Demonstrated ability to lead complex investigations and influence organizational quality strategy. (Level III)
Advanced knowledge of GMP systems, guidance documents, and state-specific compliance statutes.
Proficient in data-driven decision-making, trend analysis, and metrics tracking to drive continuous improvement.
Exceptional interpersonal skills; ability to negotiate quality standards with stakeholders and provide clear, persuasive technical guidance.
Impeccable attention to detail; expert in document control systems (MS Office/Google Workspace suite).

Responsibilities

Ensure comprehensive alignment with OMMU statutes, state medical marijuana regulations, and FDA guidelines.
Lead the seamless integration of seed-to-sale tracking data (e.g., Metrc/BioTrack), ensuring zero-error reporting.
Oversee chain of custody protocols for third-party lab compliance testing, maintaining end-to-end traceability and security.
Verify that packaging and labeling strategies strictly adhere to regulatory mandates, including potency compliance and mandatory safety warnings.
Architect, implement, and refine robust Quality Management Systems (QMS) that support scalable cultivation and manufacturing operations.
Direct the development and lifecycle management of Standard Operating Procedures (SOPs), ensuring documentation is accurate, actionable, and audit-ready.
Perform rigorous batch record reviews, raw material qualification, and quality control analysis to release products that meet premium quality standards.
Proactively manage and resolve deviations, non-conformances, and CAPA (Corrective and Preventative Actions) to drive long-term process stabilization.
Manage Internal and External Quality Alerts: Proactively investigate, document, report, and implement corrective actions for all quality incidents.
Conduct high-frequency internal audits and vendor assessments to preemptively identify operational risks.
Spearhead periodic mock recall exercises, refining rapid-response protocols to protect patient safety and company assets.
Provide oversight for facility sanitation, pest control, and hygiene protocols, ensuring an impeccable manufacturing environment.
Foster a "Quality-First" mindset throughout laboratory and production teams through targeted training programs and compliance awareness initiatives.
Act as the primary cross-functional liaison, translating complex quality data into actionable insights for leadership and operational partners.
Create and distribute training tools and resources to management teams to facilitate consistent quality training for their respective teams.