Quality Assurance Specialist

Requirements

• Auditing all processes to ensure internal and external regulations
• 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
• Ensure 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
• Write batch records for all new processes
• Assist in maintaining the PharmaCann SOP Shared Drive 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

Benefits

• Paid Time Off
• 401k Matching
• Retirement Plan
• Visa Sponsorship
• Four Day Work Week
• Generous Parental Leave
• Tuition Reimbursement
• Relocation Assistance