Quality Control Supervisor

Recently named one of Entrepreneur magazine's Top 100 Cannabis Leaders, Cresco Labs is among the largest cultivation, manufacturing and retail cannabis operators in the U.S. We provide a full suite of consistently dosed products catering to all consumers, from the novice to the connoisseur, from the medically treated to the recreational user. The company's core values emphasize educating consumers while seeking to eliminate social stigmas associated with marijuana. We have developed strong partnerships with dispensaries, law-makers, physicians, and local communities - putting Cresco in a unique position to establish a national operation in the complex and developing cannabis industry.
Cresco aims to lead the nation's cannabis industry with a focus on regulatory compliance, product consistency, and customer satisfaction. Their operations bring legitimacy to the cannabis industry by acting with the highest level of integrity, strictly adhering to regulations, and promoting the clinical efficacy of cannabis. As Cresco grows, they will operate with the same level of professionalism and precision in each new market they move in to.
Cresco Labs is seeking QA/QC Supervisors to join our manufacturing facility in Mendota, CA. As a QA/QC Supervisor, you will be responsible for performing sampling and inspection of in-process materials and finished products, and inspection of packaged orders prior to shipment. This position will also be responsible for ensuring products are being produced in a manner that meets all specifications. The ideal candidate must possess a strong attention to detail and experience working within a highly regulated industry.
Performs in-process and finished product sampling and inspection.
Inspects packaged orders to ensure correct content and quantities.
Inspects retain samples and customer return samples, as deemed necessary.
Reviews in-process batch documentation to ensure real-time compliance to product specifications, good documentation practices and written policies/procedures.
Reviews logbooks for accuracy and completion.
Performs equipment and product line clearances before and after production runs.
Discusses errors directly with line personnel and management so any corrections can be made in a timely manner.
Provide real-time feedback to operations personnel by monitoring documentation practices and overall adherence to written policies/procedures.
Performs audits as assigned by Vice President of Operations or QMS Manager. Collaborates with operational functions to troubleshoot manufacturing and production defects, CAPA, and customer complaints. Provides advice with process improvements to eliminate errors and reduce risk.
Conducts all duties in compliance with safety rules, applicable SOPs, and other applicable guidelines.
Responsible for management of site QA/QC staff.
Associate Degree preferred, 2-5 years' experience
Prior experience in highly regulated industry. Highly desirable: healthcare, medical devices, pharmaceutical, cannabis.
Prior experience in Quality Assurance or Quality Control function
Prior experience with ANSI/ASQ sampling and inspection procedures
Ability to follow written procedures and monitor others for adherence to written procedures
Strong written and verbal communication skills
Must be 21 years of age or older to apply
State and Federal Background check
No criminal history

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