COMPANY OVERVIEW
We are a medical cannabis cultivation, manufacturing and retail company dedicated to providing consistent, quality cannabis to patients across the country. Our highly-controlled, adaptive operation provides a broad range of products to variant consumers. 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.
MISSION STATEMENT
Cresco aims to lead the nation’s cannabis industry with a focus on regulatory compliance, patient safety, and satisfaction. Our 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 medical cannabis. As Cresco grows, we will operate with the same level of consideration and precision in each market they move into.
JOB SUMMARY
Cresco Labs is seeking QA/QC Supervisors to join our manufacturing facilities in Joliet, IL and Brookville, PA. 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.
CORE JOB DUTIES
- 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.
REQUIRED EXPERIENCE, EDUCATION AND SKILLS
- 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
- Detail-oriented
ADDITIONAL REQUIREMENTS
- No criminal history
- Must pass all required background checks
- Must remain compliant with all legal and company regulations for the industry