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Sombra Cosmetics

Quality Director

Career Insights for Director of Quality Assurance

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Based on New Mexico data

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What they do

A Director of Quality Assurance oversees and directs the overall operations of quality assurance within a company to ensure continuous improvement and compliance.

$149,987 / year median in New Mexico

+3% projected growth

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Job Description

Quality Director Sombra Cosmetics Albuquerque, NM Job Details Full-time From $35 an hour 18 hours ago Benefits Health insurance Dental insurance Paid time off Vision insurance Qualifications Teamwork Manufacturing facility experience Productivity software Quality audits Training & development FDA regulations Full Job Description Company Overview Sombra Cosmetics is dedicated to producing high-quality, OTC pain-relieving products that prioritize quality and reliability. With over 50 years of experience, our commitment to our high standards makes us a trusted leader in the industry among health care providers and their patients. Director of Quality Full-time | On-site | Small OTC Manufacturing Company We are seeking an experienced and driven Quality Director to lead our quality assurance and compliance efforts at our FDA-registered, cGMP-compliant facility. This is a hands-on leadership role responsible for ensuring that all products—from raw materials to finished goods—adhere to Sombra's high standards of safety, integrity, and effectiveness. Ideal candidates will have a deep understanding of cGMP requirements in the cosmetic or OTC topical space and thrive in a dynamic, collaborative manufacturing environment.
What You'll Do:
Oversee all quality operations, from raw materials to finished product. Lead a small quality team and make sure we're staying on track with regulations (FDA, cGMP, OSHA, etc.). Review and approve documentation like batch records, lab reports, and test results. Monitor production processes and make sure everything meets internal standards. Handle inspections, audits, and compliance reporting. Work closely with production and leadership to troubleshoot and improve processes. Train team members on quality and compliance practices. Maintain and enhance quality systems (CAPA, deviation, non-conformance, change control, SOP development and revision, training, documentation, etc.).
What We're Looking For:
A solid understanding of quality systems and FDA/cGMP regulations. Someone who's organized, detail-oriented, and great at solving problems. A natural leader who's comfortable managing a team and making decisions. Strong communication skills—you'll work closely with everyone from the production floor to the executive team.
Qualifications:
Bachelor's degree in Chemistry, Engineering, or a related field. 5+ years of experience in a quality role, preferably in an FDA-regulated setting. Experience in OTC or pharmaceutical manufacturing is a big plus. Comfortable using Microsoft Office and working with quality documentation systems.
Bonus Points If You:
Like being part of a small, tight-knit team. Enjoy improving processes and finding better ways to do things. Can switch between strategy and day-to-day tasks with ease.
Perks:
Flexible work environment with a collaborative team. Opportunity to make a big impact in a small company. Room to grow as the company grows.
Pay:
From $35.00 per hour Expected hours: 40.0 per week
Benefits:
Dental insurance Health insurance Paid time off Vision insurance
Work Location:
In person