Quality Coordinator

Lakeville, MA
Full Time
GP
Experienced
QUALITY COORDINATOR:
Founded in 2018 and headquartered in Boca Raton, Florida, Jushi is a vertically integrated, multi-state cannabis company that develops and operates high-end retail locations, premium brands, state-of-the-art cultivation, processing, manufacturing facilities, along with a cutting-edge online platform that is setting a new standard for a sophisticated, data-driven, modern cannabis experience. 

Since its founding in 2018, Jushi has grown from just a handful of people with an idea to more than 900 employees strong. The Company has scaled its operations in seven states, including Pennsylvania, Virginia, Massachusetts, Illinois, California, Nevada, and Ohio, and has been named one of the top five cannabis companies to work for by Cannabis Business Times.

The Company operates more than two dozen retail locations across the country under the retail brand, BEYOND / HELLO™ as well as under the recently acquired brand, Nature’s Remedy. The Company provides unparalleled in-store experience, coupled with online reservations and in-store express pickup.


Each day, Jushi team members continue to grow, cultivate, process and manufacture a comprehensive suite of cannabis brands under the names: The Bank, The Lab, Tasteology, Nira + Medicinals and Sèche, which are addressing a wide variety of consumer and patient needs across multiple states.

THE OPPORTUNITY:
The Quality coordinator will be responsible for coordinating all quality aspects of the production site and ensure all products are manufactured in compliance with 21CFR111 and cGMP requirements. This role will schedule, forecast, and track tasks from the Jushi Quality Management System (QMS). This opportunity must portray managerial skills like KPIs, Interdepartmental communications, Regulatory and In-house audit, and Managing a QMS designed for the Cannabis Industry.
  • Participate in the overall review and audit of the Quality Assurance Program to promote continual improvement.
  • Create and manage quality documents, including Standard Operating Procedures, Batch Production Records, Process Flows, and associated records.
  • Coordinate Quality trainings and coaching site-wide and provide guidance with compliance and regulatory topics.
  • Work cross-departmentally with Supply Chain to ensure the quality of incoming raw materials.
  • Collaborate with Production to achieve overall company objectives while ensuring quality standards are maintained.
  • Implement and enforce cGMP principles, at all stages of the production process.
  • Lead and initiate the troubleshooting of existing systems, equipment, and processes to improve overall product quality and food safety.
  • Support audit preparation, conduct audit and compliance activities and obtain and maintain the facility and regulatory certifications.
  • Support technical and production staff for investigations, product returns, R&D and Quality Events.
  • Provide quality guidance to employees.
  • Responsible for executing the internal audit program.
  • Develop processes and procedures to implement the quality management system.
  • Responsible for effectively communicating and escalating product quality problems to management
  • Responsible for ensuring a state of cGMP readiness for the site that ensures successful regulatory inspections.
  • Independent review and approval of batch record documentation, including validation protocols, master batch records, analytical test results, packaging, and labeling documentation.
  • Lead, coordinate and monitor the Quality Control program.
EDUCATION & EXPERIENCE:
  • Bachelor degree of Science in any field required, Master of Science degree preferred.  
  • Minimum of 5 years Quality Assurance experience
  • Experience working with regulatory policies and procedures.
  • Experience working in a regulated environment or on a team with ISO 9001 certification desired.
  • Experience with cGMP, 21CFR111, and 21CFR 110/117 desired.
OTHER DUTIES: 
Please 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.

Pennsylvania Medical Solutions, LLC 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.
 
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