Quality Control Office Administrator

Benefits

Parental leave

Not verified

Non-birth-parent leave

Not verified

Family-building benefits

• Fertility benefits: Not verified
• Adoption assistance: Not verified
• Surrogacy assistance: Not verified

Mental health support

Not verified

Relocation assistance

Not verified

Childcare support

Not verified

Learning budget

Not verified

Verification

Not verified

Salary

$16-$21/hr not verified - source not recorded; timestamp not recorded

401(k) match

Not verified

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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

38% 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

Not verified

Application

Cover letter

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Assessment

Not verified

Deadline

Not stated

Where they hire

State eligibility is not yet verified.

About this role

Quality Control Office Administrator USA - Corona, 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 QC Office Administrator, you will be responsible for reviewing and auditing documentation received from assigned co-packers, ensuring all data is accurately recorded and maintained as well as assist in other projects and tasks. The Impact You'll Make: - Review production documentation for accuracy, completeness, and compliance with established standards. - Evaluate physical and analytical lab data to determine whether product lots meet specifications for release. - Communicate promptly with co-packers regarding any discrepancies in documentation, gaps in data, missing information, or quality concerns. - Monitor and track all production that is on hold, including follow-up on developments that may impact product release decisions. - Draft and send out professional emails related to production status, documentation requests, and follow-ups with both internal and external teams. Who You Are: - High School Diploma - Additional Experience Desired: Minimum

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