GVB Biopharma is an industry-leading, vertically integrated global leader in the ever-growing hemp industry. We prioritize cannabinoid research, industry innovation, and traceable quality control. GVB operates two state-of-the-art facilities: a 30,000-square-foot food-grade hemp processing facility in Central Oregon and a 40,000-square-foot white-label consumer product manufacturing facility in Las Vegas.
JOB SUMMARY:
This position requires the ability to lead and train Quality professionals in the
appropriate application of standards including ISO 9001:2015 and cGMP and support both internal and external customers.
ESSENTIAL DUTIES AND RESPONSIBILITIES.
*Other assignments, projects, and duties may be required:
Primary responsibilities include:
- Leads in the development of a climate of quality and safety, seeking continuous
improvement, providing sound vision and guidance in the application of Quality standards
- Administrate and manage the Quality Management System, driving to completion events such as corrective actions, change control, deviations, nonconforming product, and audit reports
- Aid in determining root cause for nonconforming events and evaluate corrective and preventive actions for lifecycle effectiveness
- Author or approve key Quality System documents
- Author, approve and defend as applicable corrective actions
- Effectiveness monitoring of site Quality Systems, presenting during the management review cycle
- Assist and support Audit Program to evaluate compliance requirements and identify areas requiring corrective action or opportunities for improvement
- Assure timely completion of corrective and preventive actions
- Maintain and support procedures to ensure the compliance of all products and packaging
- Support supplier approval program, setting requirements for raw material and component products and tracking supplier compliance
- Oversee product development procedures to identify deviations from quality standards
- Product stability study coordination
- Supervise direct reports, providing guidance and feedback
- Execute and manage processes to ensure effective documentation control
- Recall and mock recall coordination
PREFERRED QUALIFICATIONS:
- Bachelor’s degree in chemistry, biology, or related field with seven years of professional experience in the pharmaceutical, dietary supplement, or food industry, preferably with five years in a Quality role
- Supervisory or management experience
- ASQ certified CMQ/OE, CQE, CQA, or CFSQA
- Proficient skills in, G Suite, Video Conferencing, Excel, and Word
- Strong organizational skills and the ability to work effectively with a team
Job Type: Full-time
Pay: $75,000.00 - $85,000.00 per year
Benefits:
- Dental insurance
- Employee discount
- Health insurance
- Paid time off
- Vision insurance
Schedule:
Supplemental Pay:
COVID-19 considerations:
GVB has measures and regulations in place to ensure the health and wellbeing of our employees. We have established social distancing and mask requirements and have been following all state and local regulations.
Application Question(s):
- Please list any relevant certifications as required by the Job Description.
- Our facility is located in Grass Valley, OR. Are you willing and or able to commute/relocate to Grass Valley?
Education:
Experience:
- Quality Assurance: 5 years (Preferred)
Work Location:
Work Remotely: