Quality Assurance Specialist
Company
PharmaCann
Location
Detroit, MI
Type
Full Time
Job Description
PharmaCann, Inc. owns and operates best-in-class production facilities and retail dispensaries for cannabis-based products. We currently operate in the States of Illinois, New York, Massachusetts, Ohio, Pennsylvania, Maryland, Colorado and Michigan as a medical and/or adult use cannabis provider to patients and customers. We are looking for energetic, results-driven individuals to join our rapidly growing team and industry.
Job Summary
With guidance and supervision from the QA Regional Director, this position supports the Quality Assurance organization and is responsible for the daily execution of all medical cannabis quality processes as assigned for both operations. The incumbent will work within company standards and the applicable state regulations.
Duties and responsibilities or (Essential Functions)
- Auditing all processes to ensure both internal and external regulations standards are being adhered to.
- Floor presence throughout the day in all manufacturing areas.
- Oversee cleaning procedure, inspecting equipment and work area, ATP surface testing of the addition processes now in production.
- Ensuring auditing and manufacturing documentation is kept up to date.
- Review of cGMP documents to ensure company processes comply and maintain Quality Assurance documentation.
- Develop the standard measurements for processes to be compared against then inspect and test processes and procedures.
- Write Standard Operating Procedures (SOPs) for the new manufacturing process, send them out for review then approval finally entering them into the QMS Veeva system
- Write batch records for all new processes send them out for review then approval finally entering them into the QMS Veeva system
- Assist in maintaining the QMS Veeva System.
- Increase raw materials entering the site where Quality will need to do inspection of and release the materials to manufacturing.
- Assist in training production staff on quality all new procedures, protocols, and documentation
- Coordinate investigation of quality issues with manufacturing and customer complaints
- Review, approve and communicate all investigation root cause and follow up with corrective action with stakeholders.
- Drive continuous improvement of core processes to ensure manufacturing quality is maintained while efficiency is optimized.
- Initiate annual reviews of SOPs and batch records.
- Assist the QA in Pennsylvania when needed.
- Projects a positive image of the organization to employees, customers, industry, and community
- Embodies the culture, values, and tenets of PharmaCann and full support of our purpose, goal, and key objectives
- All other duties as assigned
Qualifications
- Education/Experience:
- High School required, plus 5 years related work experience or Associate’s degree, plus three years related work experience
- Experience having worked in a cannabis and/or manufacturing environment strongly preferred
- Age: State law requires that applicants be 21 years old to work for a cultivation center
- Certifications: None
Working conditions
Work in a manufacturing environment.
Notice: To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed above are representative of the knowledge, skill, and/or ability required and are not intended to be an exhaustive list of all duties, responsibilities or qualifications associated with this job.
We are an Equal Employment Opportunity Employer. Qualified applicants will receive consideration for employment without regard to race color, religion, sex, national origin, sexual orientation, gender identity, disability, protected veteran status or any other status protected by applicable law.
Date Posted
03/16/2024
Views
9
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