Quality Director - Personal Care or Cosmetics Products Manufacturing - Dallas/DFW Area
Company: Naturich Labs, Inc.
Location: Garland
Posted on: January 19, 2026
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Job Description:
Job Description Company Description Naturich Labs is a leading
contract manufacturer of natural and organic personal care
products, serving a wide range of clients in skincare, haircare,
bath & body, and wellness categories. Our innovative approach
combines extensive R&D knowledge with modern formulation
science to deliver effective, market-ready products. As we continue
to grow, our commitment to quality and innovation remains at the
heart of everything we do. Naturich is known for its innovative
approach to product development, utilizing cutting-edge research to
blend traditional raw material science with modern science.
Benefits for this position include: Medical, Dental, Vision, Paid
Holidays, Paid Time Off, 401k with match, professional development
in a high-growth organization, work-life balance, a positive work
environment, and much more. Quality Director - Personal Care or
Cosmetics Products Manufacturing - Dallas/DFW Area Position
Summary: We are seeking a seasoned and solutions-oriented Quality
Director to lead the evolution and expansion of our Quality
division during a pivotal period of growth. This high-impact
leadership role requires a tenured professional with a strong
foundation in beauty, personal care, or OTC manufacturing and a
proven ability to manage FDA and client-facing audits. The ideal
candidate is a strategic yet hands-on leader who can drive
operational excellence, implement scalable quality systems, and
inspire teams through change management and continuous improvement.
This individual will play a key role in shaping a best-in-class
quality culture that safeguards product integrity, ensures
regulatory compliance, and supports Naturich’s commitment to
innovation and customer trust. Key Responsibilities: ? Lead,
mentor, and develop the Quality Assurance and Quality Control teams
to build a culture of ownership, accountability, and continuous
improvement. ? Design, implement, and enhance scalable quality
systems aligned with cGMP, FDA 21 CFR Parts 210/211, ISO 22716, and
other applicable standards. ? Champion audit readiness and serve as
the primary contact for FDA, regulatory, and client audits,
ensuring timely and thorough responses to findings and corrective
actions. ? Own the development and execution of validation
processes (equipment, process, cleaning, etc.) and ensure timely
reporting of nonconformances, root cause analyses, and trending of
quality metrics. ? Collaborate cross-functionally with R&D,
Operations, and Project Management to ensure quality integration
throughout new product development, tech transfers, and scale-ups.
? Interpret quality control results and provide clear, actionable
feedback to production teams. ? Supervise the collection and
analysis of production samples to ensure quality standards are met.
? Lead the team through organizational growth and change, balancing
structure with agility to support evolving business needs. ?
Standardize and maintain GMP-compliant SOPs, documentation, and
internal processes to support audit readiness and traceability. ?
Track, analyze, and report on quality performance metrics to drive
transparency and continuous improvement. ? Maintain awareness of
internal and external trends, opportunities for improvement, new
customers, changes in markets, new industry developments, evolution
of standards and industry practices, threats and risk to the
organization. Qualifications & Experience: ? 8–10 years of
progressive experience in quality management within contract
manufacturing, beauty/personal care, or OTC regulated environments
with at least 3 years in a leadership role. ? Proven success
managing FDA, client, and third-party audits, including direct FDA
interaction and remediation leadership. ? Bachelor’s degree in a
scientific or engineering discipline required; advanced degree or
certifications (e.g., ASQ CQE, CQA, or CMQ/OE) preferred . ? Deep
working knowledge of FDA 21 CFR 210/211, OTC monograph system,
cosmetic regulations, and quality standards (ISO 22716, ISO 9001).
? Demonstrated ability to lead through growth and change, establish
new systems, and elevate team performance. ? Strong communication,
documentation, and problem-solving skills with an ability to
influence at all organizational levels. ? Strong attention to
detail and organizational skills, with the ability to manage
multiple projects and deadlines effectively. ? Excellent written
and verbal communication skills, with the ability to communicate
complex quality concepts clearly and effectively. ? Advanced skills
in documentation control, SOP development, and root cause analysis.
? Proficient in ERP systems, QMS platforms, document management
systems, and standard productivity tools (Microsoft Office/Google
Workspace). What We’re Looking For: ? A builder and change agent -
You thrive in scaling environments, building systems and processes
that support growth without compromising quality. ? A hands-on
leader – You’re comfortable operating at both strategic and
operational levels to ensure successful execution. ? A
collaborative communicator – You inspire trust, clarity, and
alignment across departments and leadership levels. ? A champion
for quality - You are deeply committed to delivering products that
meet the highest standards and take pride in building systems that
uphold and enhance the company’s reputation through operational
excellence.
Keywords: Naturich Labs, Inc., Chapel Hill , Quality Director - Personal Care or Cosmetics Products Manufacturing - Dallas/DFW Area, Science, Research & Development , Garland, North Carolina
