Quality Supervisor

• Be Part of a Growing Health & Wellness Industry
• Hands-On Impact in a Fast-Paced Manufacturing Environment

About Our Client

Our client is a growing dietary supplement manufacturer focused on producing high-quality health and wellness products in a GMP-regulated environment.

Job Description

Quality Systems & Compliance

• Supervise daily Quality Assurance and Quality Control operations across manufacturing, packaging, warehousing, and sanitation functions.
• Ensure compliance with current Good Manufacturing Practices (cGMP), FDA regulations, SOPs, and internal quality standards.
• Maintain and improve quality management systems, procedures, and documentation.
• Support customer, regulatory, and third-party audits and inspections.
• Monitor quality metrics and implement corrective actions when necessary.
• Ensure proper completion and review of batch records, production documentation, and quality records.

Product Quality Oversight

• Conduct and supervise incoming material, in-process, and finished product inspections.
• Review product specifications and ensure compliance with established quality requirements.
• Investigate product deviations, non-conformances, customer complaints, and quality incidents.
• Support root cause investigations and implement corrective and preventive actions (CAPAs).
• Monitor environmental, sanitation, and quality control programmes to ensure product safety and quality.

Team Leadership & Development

• Lead, coach, and develop quality technicians and inspectors.
• Conduct training on quality procedures, GMP requirements, documentation practices, and food safety principles.
• Manage employee performance, scheduling, and workload distribution.
• Promote a culture of quality, accountability, and continuous improvement throughout the facility.
• Collaborate with cross-functional teams to resolve quality concerns and improve processes.

Audit & Regulatory Support

• Participate in internal audits and prepare documentation for external inspections.
• Assist in maintaining audit readiness at all times.
• Ensure compliance with FDA regulations, GMP requirements, and applicable industry standards.
• Support supplier qualification and vendor quality management activities as needed.
• Review quality trends and recommend improvements to minimise risks and improve compliance.

Continuous Improvement

• Identify opportunities to improve product quality, process efficiency, and overall compliance.
• Analyse quality data and performance metrics to support strategic decision-making.
• Assist with validation, verification, and change control initiatives.
• Support implementation of new quality systems, programmes, and operational improvements.
• Partner with Manufacturing, Operations, Maintenance, and Supply Chain teams to drive quality excellence.

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. the company will consider for employment qualified applicants with criminal histories in a manner consistent with the Los Angeles Fair Chance Initiative for Hiring Ordinance. 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.


The Successful Applicant

A successful Quality Supervisor should have:

• High school diploma or equivalent.
• 3+ years of quality assurance, quality control, or quality supervision experience in a regulated manufacturing environment.
• Prior leadership or supervisory experience.
• Working knowledge of cGMP regulations and quality systems.
• Experience investigating deviations, non-conformances, and CAPAs.
• Strong understanding of quality documentation and record-keeping requirements.
• Excellent organisational, communication, and problem-solving skills.
• Proficiency with Microsoft Office and quality management software.
• Bachelor's degree in Quality, Food Science, Biology, Chemistry, Engineering, or a related field.
• Experience within dietary supplements, nutraceuticals, pharmaceuticals, food manufacturing, or consumer packaged goods.
• Knowledge of FDA requirements, supplier quality programmes, and audit management.
• Experience with Lean Manufacturing, Six Sigma, or other continuous improvement methodologies.
• Bilingual English/Spanish.

What's on Offer

• Competitive annual salary ranging from $90,000 to $110,000.
• Comprehensive benefits package.
• Permanent position with opportunities for professional growth.
• Make a significant impact on product quality, regulatory compliance, and customer satisfaction within a growing health and wellness manufacturing organisation.
• Join a collaborative team committed to quality excellence, continuous improvement, and professional development.
• Gain exposure to a dynamic, highly regulated industry with strong long-term growth opportunities.
• Play a key leadership role in ensuring products meet the highest standards of safety, quality, and compliance.

Interested? Apply today.

Contact

Brinn Borowsky

Quote job ref

JN-092026-7102482