Job Description
Job Overview
We are seeking an experienced and hands-on Quality Manager to oversee the quality systems and continuous improvement initiatives within a regulated manufacturing environment. This position will lead the quality assurance, quality control, lab testing, document control, and validation teams while ensuring compliance with FDA, cGMP, and ISO 9001 standards. The ideal candidate will be a strategic thinker who can also operate in a highly detailed, hands-on capacity.
Key Responsibilities
Ensure the quality management system complies with customer, regulatory, and internal standards including FDA, cGMP, and ISO 9001
Evaluate and monitor supplier quality systems
Oversee inspections and testing of incoming raw materials and finished products
Lead the quality assurance, quality control, lab, validation, and documentation teams
Manage internal audits and external regulatory inspections
Analyze quality data, lead investigations, and drive corrective and preventive actions
Coordinate and report performance metrics to executive leadership
Implement and improve processes in alignment with operational excellence goals
Supervise product hold procedures and recall protocols
Ensure accurate calibration and use of monitoring and measuring equipment
Stay up to date with evolving regulatory and industry requirements
Qualifications
Bachelor's degree in chemistry is required
Certified Manager of Quality or equivalent certification is required
Minimum fifteen years of experience in regulated industry quality roles
At least five years of direct experience with 21 CFR 210 and 211 and ISO 22716
Experience in cosmetics or personal care manufacturing is highly preferred
Lean Six Sigma green belt or similar experience is desired
Proficiency with LIMS is a plus
MBA or other advanced degree is a plus
Core Skills and Competencies
Strong leadership and team development abilities
Excellent written and verbal communication skills
Hands-on approach to managing compliance and process improvement
Strong analytical thinking and data-driven decision-making
Experience managing internal audits, document control, and product testing
Advanced knowledge of Microsoft Office and quality management systems
Work Environment
Full-time onsite role in a manufacturing environment
Typical work schedule is Monday through Friday
Requires occasional standing, walking, or lifting up to 25 pounds
How to Apply
Send your resume to Description
All About Personnel was founded with the goal of providing high quality management consulting, and staffing services to small, medium, and large sized companies. Our primary objective in our consulting and staffing engagement is to improve our client’s profitability by increasing productivity, improving quality and competitiveness and reducing turnover by finding the right talent in your industry. During the past twenty years, staffing along with the talent has changed significantly and it is our goal to assist our clients by helping them improve their profitability by increasing their efficiency rate and reducing turnover. Our client scope is leading companies in consumer manufacturing, food manufacturing, wholesale, distribution, transportation, government, and commercial printing.
Full-time