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Quality Control Coordinator

Monster Beverage - USA - Norwalk, CA

Posted Jun 11, 2026

Benefits

Parental leave
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Non-birth-parent leave
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Family-building benefits
  • Fertility benefits: Not verified
  • Adoption assistance: Not verified
  • Surrogacy assistance: Not verified
Mental health support
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Relocation assistance
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Childcare support
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Learning budget
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Verification
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Salary
$18-$25/hr not verified - source not recorded; timestamp not recorded
401(k) match
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Market context

U.S. role benchmark (BLS OEWS)
$61,842 U.S. median for this role
Projected growth (BLS Employment Projections)
+1.9% - Slower

28% below the BLS role benchmark for operations aggregate.

Matched to SOC 11-1021 - Operations aggregate by role bucket.

Source: U.S. Bureau of Labor Statistics, OEWS, May 2024 and Employment Projections, 2024-2034.

Schedule

Shift type
Not verified
Weekend work
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Application

Cover letter
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Assessment
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Deadline
Not stated

Where they hire

State eligibility is not yet verified.

About this role

Quality Control Coordinator USA - Norwalk, CA About Monster Energy: Forget about blending in. That's not our style. We're the risk takers, the trailblazers, the gamechangers. We're not perfect and we don't pretend to be. We're raw, unfiltered, and a bit unconventional. Our drive is just like our athletes, unrivaled. The power is in your hands to define what success looks like and where you want to take your career. It's not just about what we do, but about who we become on along the way. We are much more than a brand here. We are a way of life, a mindset. Join us. A Day in the Life: In the position of Coordinator, QC you will be responsible for managing and maintaining programs that ensure Monster Energy is compliant with all federal, state and local requirements. The Impact You'll Make: - Responsible for managing and maintaining programs that ensure Monster Energy is compliant with all federal, state and local requirements. Work is centered in the support of the QC leadership team and Testers. - Assist in the remediation of all deviations, non-conforming material and complaints. Coordinate 3rd party lab testing submissions for complaint investigations, country submissions, and validation efforts. - Oversee the shelf-life extension program for raw materials. Participate in technical reviews necessary to ensure Good Manufacturing Practices (GMP) compliance, including; raw material and finished good specifications, label approval, master manufacturing records, etc. - Conducts internal GMP/Hazard Analysis and Critical Control Points (HACCP)/Standard Operating Procedures (SOP) training as required.

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