CBD VAPE -Quality Assurance Specialist (Product Development) (Boca, FL) Job at Heartland Works LLC
CBD VAPE QUALITY ASSURANCE SPECIALIST (Product Development)
ABOUT THE JOB
Heartland Works LLC (“HL” and “Company”) is currently seeking a highly motivated and forward-thinking Quality Assurance Specialist to join our team! You will be a key contributor to our enterprise-wide initiative.
The Quality Assurance Specialist is responsible for developing SOP and monitoring the quality processes of our production facilities to ensure the quality assurance of our product regarding filling, packaging, shipping and compliance with CBD safety standards and regulations.
We are looking for someone with a proven track record and hunger for success in the e- cigarette and cannabis industry. This position will conduct internal audits, establish verification steps for CBD safety processes and all required record-keeping for Company QA development.
The QA Specialist will work closely with production managers at contracted facilities, establishing specifications and monitoring the production processes to ensure they meet quality, standards and requirements of HW and the CBD safety regulations.
RESPONSIBILITIES
- 3+ years of QA experience.
- Deep knowledge of the cannabis industry.
- Ensure incoming and outgoing products adhere to set quality standards.
- Review and ensure accuracy of submitted batch records.
- Prepares reports by summarizing data.
- Crafts and reviews standard operating procedures based on safety and regulatory
- requirements.
- Leads regular audits of quality and safety standards.
- Review in-house and vendor calibrations for accuracy and adherence to company and
- industry guidelines.
- Initiates investigations into quality issues and sees them through to closure.
- Act as a subject matter expert in all aspects of quality and regulatory concerns or
- questions
PREFERRED QUALIFICATIONS
- 5+ years of QA experience.
Deep knowledge of the cannabis industry.- Excellent reading, written and oral communication skills.
- Ability to write detailed specs, standards and operating procedures.
- Strong time and project management skills.
- Stellar attention to detail.
- Familiar with cGMP and industry guidelines.
- Outstanding organizational skills.
- Familiarity with Google Sheets and/or Excel
NONE PHYSICAL REQUIREMENTS:
- Standing for long periods of time.
- Bending, stooping, climbing ladders.
- Lift up to 60lbs at a time.
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