Quality Assurance Specialist – Trulieve, INC – Quincy, FL

Quality Assurance Specialist

Location: Quincy, FL

Reports to: Quality Assurance Manager

Position Summary

The Quality Assurance Specialist is responsible for ensuring the quality of our company?s products and assisting in the maintenance and continuous improvement of our company?s internal Quality System. This individual will serve as a primary Quality Assurance resource for department supervisors for problem identification, and resolution.

Essential Duties and Responsibilities

The essential functions include, but are not limited to the following:

  • Drive a culture of Quality and Compliance
  • Assist in the development of statistical data and product specifications to determine present standards and establish proposed quality and reliability expectancy of finished product
  • Review test results and confirm compliance with specifications
  • Ensure goods and products comply with company standards, GMP, and PA Department of Health regulations
  • Assist team members in Investigations, Root Cause Analysis procedures and implementation of effective CAPAs through ISOlocity
  • Analyzing regulatory requirements to assess their effect on the internal Quality System
  • Core member of Internal Auditing team
  • Perform inspections at various points in the manufacturing process
  • Develop/maintain/improve inspection data reports
  • Write, update, and maintain quality SOP’s (Standard Operating Procedures) through ISOlocity
  • Investigate and track customer complaints regarding quality
  • Communicate quality and/or compliance concerns with urgency
  • Identify possible areas for improvement in quality control processes
  • Performing other duties as requested

Minimum Qualifications (Knowledge, Skills, and Abilities)

  • Bachelor?s degree with a minimum of 2 years Quality related experience in a manufacturing environment; or Associates degree with 4 years of Quality related experience; or a minimum of 5 years of Quality related experience
  • Pharmaceutical or food manufacturing experience is preferred
  • Strong computer skills with working knowledge of Microsoft Office Suite and manufacturing management systems
  • Familiarity with Quality System Practices, such as Document Control, Auditing, Investigations, and CAPAs
  • Possess solid root cause analysis and problem solving capability.
  • Independent self-starter with decision-making ability
  • Strong attention to detail
  • Excellent oral and written communication skills, with proven ability to share information effectively with all levels
  • Ability to keep calm under pressure
  • Ability to prioritize activities under tight deadlines
  • Understanding of test equipment
  • Excellent organizational skills
  • Desired: Knowledge of GMP requirements and HACCP

Apply Here


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