Cannabis jobs at Green Rock Hemp Holdings, LLC

This individual is responsible for supporting quality-related GMP activities occurring at manufacturing, and supply chain. This position will report to Quality Assurance Manager and work closely with Supply Chain representatives to support disposition activities for GMP materials (e.g. quality control workflows). This position will support the Quality Assurance Manager in ensuring products are being produced in a manner that meets all specifications. You will also support efforts to identify potential quality risks and working with manufacturing operations personnel to develop improvement opportunities. The Quality Assurance Associate will also provide quality support for related functions, including product manufacturing and quality system support. The successful candidate is self-motivated, independent, highly organized, able to work in a small team environment and adjust direction based on changing project/corporate priorities.

CORE JOB DUTIES

· Provide QA support for the review of analytical protocol, report and method review

· Support review for disposition of GMP materials, reviewing master and executed batch records, quality documents and other related paperwork

· Support release and disposition for Finished Product

· Review various documents such as batch records, technical reports, data, stability protocols and other GxP documents as needed

· Maintain logs for Quality systems, such as CAPA, Deviations, Investigations and Release Records

· Support the identification and investigation of quality related complaints or deviations, identifying and resolving root causes

· Support external/internal audits and inspections

REQUIRED EXPERIENCE, EDUCATION, SKILLS

· Bachelor’s Degree, minimum 1 years’ experience in Pharmaceutical Industry in a related quality assurance role, or the equivalent combination of education, training and experience.

· Experience with reviewing and dispositioning GxP materials

· Ability to identify technical problems and suggest resolution of the issues

• Ability to follow written procedures and monitor others for adherence to written procedures

• Ability to create or update written procedures with site operations personnel

ADDITIONAL REQUIREMENTS

• Must be 21 years of age or older to apply

• Must comply with all legal or company regulations for working in the industry

Job Type: Full-time

Pay: $15.00 - $20.00 per hour

Benefits:

• Paid Time Off

Experience:

• Quality Assurance/Quality Control: 1 year (Preferred)
• pharaceutical industry: 1 year (Preferred)

Education:

• Bachelor's (Required)

Work authorization:

• United States (Required)

Work Location:

• One location

This Job Is Ideal for Someone Who Is:

• Dependable -- more reliable than spontaneous
• Detail-oriented -- would rather focus on the details of work than the bigger picture

This Company Describes Its Culture as:

• Detail-oriented -- quality and precision-focused
• Innovative -- innovative and risk-taking
• Team-oriented -- cooperative and collaborative

Schedule:

• Monday to Friday
• Day shift

Company's website:

• https://www.greenrockhempholdings.com/

Benefit Conditions:

• Only full-time employees eligible

Work Remotely:

• No

Apply for this job with Green Rock Hemp Holdings, LLC

Apply now →

By clicking the "Apply now" button, you'll be leaving Fazow and going to an external job application page for this company. Please research all companies before applying. When applying for jobs, you should NOT have to pay to apply. Fazow accepts no liability or responsibility as a consequence of any reliance upon information on external sites or in jobs listed on fazow.com.