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Director of QA/QC Cosmetics

Michael Page Ventura, CA (Onsite) Full-Time
$150,000 - $185,000/Year

We are seeking an experienced and strategic Director of Quality to lead our quality assurance and quality control functions across all aspects of our cosmetic manufacturing operations. This role will be responsible for ensuring our products meet the highest standards of quality, safety, regulatory compliance, and customer expectations. You will work cross-functionally with R&D, Operations, Regulatory, and Supply Chain to build and scale quality systems that support growth.

Client Details

My client is a leading innovator in cosmetic manufacturing, committed to delivering high-quality beauty and personal care products to global brands. With a passion for excellence, innovation, and sustainability, we partner with our clients to bring their visions to life through cutting-edge formulation, precision manufacturing, and strict regulatory compliance.

Description

  • Lead and oversee all Quality Assurance (QA) and Quality Control (QC) operations across manufacturing facilities.
  • Develop, implement, and manage comprehensive quality systems in accordance with FDA, ISO 22716 (GMP for cosmetics), and other applicable regulations and standards.
  • Drive continuous improvement initiatives to enhance product quality, reduce non-conformances, and improve manufacturing efficiency.
  • Partner with R&D and Regulatory Affairs to ensure new product introductions meet quality and compliance requirements.
  • Serve as the primary point of contact for internal and external audits, including client inspections and regulatory bodies.
  • Lead root cause analysis and CAPA investigations for product or process deviations.
  • Implement robust supplier quality programs and ensure incoming materials meet specifications.
  • Build and mentor a high-performing quality team, fostering a culture of accountability, training, and operational excellence.
  • Establish and report on key quality metrics and KPIs to leadership, identifying trends and recommending corrective actions.
  • Maintain documentation systems for batch records, specifications, SOPs, and testing protocols.

Profile

  • Bachelor's degree in Chemistry, Biology, Engineering, or related field (Master's or advanced degree preferred).
  • 8-12+ years of quality experience in cosmetic, personal care, pharmaceutical, or regulated CPG manufacturing, with at least 3-5 years in a leadership role.
  • Deep knowledge of FDA regulations, ISO 22716, GMP, and other quality and regulatory standards relevant to cosmetics.
  • Proven experience with quality systems implementation, audit management, CAPA processes, and product testing protocols.
  • Strong leadership and team-building skills with the ability to drive cross-functional collaboration.
  • Excellent problem-solving, organizational, and communication skills.
  • Experience working in fast-paced, growth-oriented environments and scaling systems effectively.

Job Offer

  • 3 weeks of vacation plus Holiday Break
  • Bonus
  • 401k match

MPI does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity or expression, national origin, age, disability, veteran status, marital status, or based on an individual's status in any group or class protected by applicable federal, state or local law. MPI encourages applications from minorities, women, the disabled, protected veterans and all other qualified applicants.

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Salary Details

This salary was provided in the Job Posting.
$150,000-$185,000
Yearly Salary

Job Snapshot

Employee Type

Full-Time

Location

Ventura, CA (Onsite)

Job Type

Engineering, Manufacturing, QA - Quality Control

Experience

Not Specified

Date Posted

04/08/2025

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