Onsite Quality Control Specialist — Moab, UT

The-Synergy-Company-of; Moab (UT); On-site; USD 39,000 - 52,000; Full time

Job summary

The Synergy Company is seeking a Quality Control Specialist to join our Moab, Utah quality team. This hands-on role supports quality systems, investigations, regulatory activities, production, and laboratory operations to ensure our products meet high internal and industry standards.

You will perform internal audits, document findings, and help maintain CAPA/deviation programs while coordinating with lab personnel and production teams in a 40-hour onsite schedule.

Qualifications

• High school diploma not explicitly required (see preferred)
• Bachelor’s degree in a scientific field preferred
• Experience with food production processes and systems is a plus
• Familiarity with cGMP, HARPC, FSMA, Kosher, and Certified Organic guidelines is preferred

Responsibilities

• Perform internal audits and regular inspections in production areas
• Document audit findings and communicate quality concerns to leadership
• Maintain CAPA and deviation programs with tracking and closure
• Investigate temperature/humidity readings, returns, defects, and nonconforming materials
• Support QA activities for wholesale customers and ingredients including regulatory documentation
• Assist with finished-goods stability studies and data analyses
• Coordinate with laboratory personnel and send samples to third-party labs
• Develop and improve laboratory methods and equipment
• Participate in continuous quality improvement efforts

Skills

Attention to detail

Critical thinking

Organization

Judgement

Communication

Math & computing

Prioritization

Team collaboration

Quality improvement

Education

Bachelor’s degree in a scientific field

Job description

The Synergy Company is seeking a Quality Control Specialist to join our Moab, Utah quality team. This hands-on role supports quality systems, investigations, regulatory activities, production, and laboratory operations to ensure our products meet high internal and industry standards.

You will perform internal audits, document findings, and help maintain CAPA/deviation programs while coordinating with lab personnel and production teams in a 40-hour onsite schedule.