Quality Manager

Want to make a meaningful difference in peoples’ lives while earning a competitive salary? At Jushi Holdings Inc. ”) (CSE: JUSH) (OTCQX: JUSHF), we are shaping the future of the cannabis industry, the fastest growing jobs sector in the U.S. This role will need to be trained to fulfill Quality Manager duties and requirements as needed for future state redundancy and planning for work related travel and vacation coverage. This will begin the team building for additional trained management level ready personnel as the site continues to grow.

WHAT YOU WILL DO:

• Provide oversight of Quality Assurance and Quality Control activities at the site level, including manufacturing, packaging, labeling, and holding operations.
• Approve or reject procedures, specifications, controls, test methods, validations, and results impacting product quality.
• Conduct internal audits, deviation investigations, root cause analysis, CAPAs, and OOS reviews.
• Serve as the site authority on compliance with FDA 21 CFR Part 111 and 18VAC110-60-10 et seq.
• Supervise document control processes and maintain GMP records as per regulatory standards.
• Review and approve Master Manufacturing Records (MMRs), Batch Production Records (BPRs), and Certificates of Analysis (COAs).
• Monitor calibration and preventive maintenance of laboratory and production equipment.
• Collaborate with cross-functional teams to ensure product quality from raw material receipt to product release.
• Maintain and manage sample retention programs and stability studies.
• Lead risk assessments and change control processes.
• Train and mentor QA team members; act as SME or system owner where applicable.
• Interface with regulatory bodies and lead readiness for inspections.

WHAT WE ARE LOOKING FOR:

• Bachelor’s degree in a technical field (e.g., Chemistry, Biology, Engineering)
• 2–5 years of Quality Assurance or Quality Control experience in a regulated manufacturing environment; experience in cannabis, pharmaceuticals, or dietary supplements preferred
• Demonstrated experience managing GMP compliance, quality systems, and regulatory audits
• Familiarity with FDA 21 CFR 111, ICH Q guidelines, and Virginia Board of Pharmacy regulations
• Experience with CAPA, deviation, and change management systems
• Strong leadership, communication, and problem-solving skills
• Ability to lift 50 lbs. and perform duties in both office and production environments
• Proficiency in Microsoft Office and electronic quality systems (EDMS, QMS software, etc.).

WHAT WE HAVE TO OFFER OUR EMPLOYEES AT JUSHIWe offer benefit packages that may include Medical, Dental, Vision, Life, Short, and Long Term Disability, Flexible Spending Accounts, Paid Time Off, Paid Holidays, and 401(k). BONUS DUTIES YOU SHOULD UNDERSTANDPlease note this job description is not designed to cover or contain a comprehensive listing of activities, duties, or responsibilities that are required of the employee for this job. Duties, responsibilities, and activities may change at any time with or without notice. Jushi is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, sex, sexual orientation, gender identity or expression, religion, national origin or ancestry, age, disability, marital status, pregnancy, protected veteran status, protected genetic information, political affiliation, or any other characteristics protected by local laws, regulations, or ordinances.