QUALITY ASSURANCE SPECIALIST
: Job Details :


QUALITY ASSURANCE SPECIALIST

PharmaCann

Location: all cities,NY, USA

Date: 2024-11-02T07:18:22Z

Job Description:

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.

Pay for this role starts at $24/hour

Duties and responsibilities or (Essential Functions)

  • Auditing all processes to ensure both internal and external regulations (New York State Office of Cannabis Management) 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.
  • Performing label approvals on all batches.
  • Coordinate third party testing with the processing and flower pack teams and fill out the third-party necessary documentation for testing.
  • Ensure all required third party compliance testing is completed for each batch of product produced to ensure all batches meet or exceed state mandated requirements before being handed off to the proper packaging department.
  • Enter batches into NAV to when samples are taken from our facility or moved to a new designation and releasing the product to the vault for sale.
  • 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 Pharmacann SOP SharedDrive system
  • Write batch records for all new processes send them out for review then
  • Assist in maintaining the PharmaCann SOP Shared Drive system
  • Inspect raw materials coming on site to provide assurance that all raw materials used in the manufacturing process meet the specifications for quality, safety, and effectiveness before they are used in 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
  • Travel to Pennsylvania
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