Michael Page
Director of Quality - Packaging/Consumables - Glassboro, NJ
Michael Page, Glassboro, New Jersey, United States, 08028
Director Quality Packaging Consumables
Join an industry leader with a high performance product portfolio. My client is a global manufacturer and supplier of premium packaging solutions and consumables for the life sciences industry. They have a culture of quality, innovation, and operational excellence, seeking to deliver not only superior products but also integrated services that help customers accelerate scientific discovery and ensure regulatory compliance. Job Description
Develop and oversee execution of quality strategy aligned with company goals and regulatory requirements (e.g., ISO 9001, ISO 13485, FDA, cGMP). Lead and mentor the Quality Assurance, Quality Control, and Regulatory Affairs teams across multiple manufacturing sites. Drive continuous improvement initiatives across production and quality functions using lean, Six Sigma, and other data-driven methodologies. Ensure compliance with all applicable national and international standards and regulations related to life sciences and laboratory product manufacturing. Maintain and enhance the company's Quality Management System (QMS), including audits, CAPAs, document control, and training. Interface with customers and regulatory agencies during audits, inspections, and quality-related discussions. Establish, track, and report key quality performance metrics (e.g., customer complaints, returns, defects, audit findings). Collaborate with R&D, Manufacturing, Supply Chain, and Commercial teams to ensure product quality from design through delivery. Champion a strong quality culture across all levels of the organization. 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
Bachelor's degree in Engineering, Life Sciences, Chemistry, or related field (Master's preferred). 10+ years of progressive quality leadership experience in a GMP/Manufacturing setting. Demonstrated experience managing regulatory compliance and quality systems (e.g., ISO 9001). Proven leadership and change management skills with cross-functional teams in multi-site environments. Certified Quality Auditor (CQA), Six Sigma, or similar certifications are a plus. Strong analytical, communication, and problem-solving skills. What's on Offer
Competitive Base Salary Bonus Potential Strategic Ownership of Quality Organization Competitive Benefits including 401k Company Match
Join an industry leader with a high performance product portfolio. My client is a global manufacturer and supplier of premium packaging solutions and consumables for the life sciences industry. They have a culture of quality, innovation, and operational excellence, seeking to deliver not only superior products but also integrated services that help customers accelerate scientific discovery and ensure regulatory compliance. Job Description
Develop and oversee execution of quality strategy aligned with company goals and regulatory requirements (e.g., ISO 9001, ISO 13485, FDA, cGMP). Lead and mentor the Quality Assurance, Quality Control, and Regulatory Affairs teams across multiple manufacturing sites. Drive continuous improvement initiatives across production and quality functions using lean, Six Sigma, and other data-driven methodologies. Ensure compliance with all applicable national and international standards and regulations related to life sciences and laboratory product manufacturing. Maintain and enhance the company's Quality Management System (QMS), including audits, CAPAs, document control, and training. Interface with customers and regulatory agencies during audits, inspections, and quality-related discussions. Establish, track, and report key quality performance metrics (e.g., customer complaints, returns, defects, audit findings). Collaborate with R&D, Manufacturing, Supply Chain, and Commercial teams to ensure product quality from design through delivery. Champion a strong quality culture across all levels of the organization. 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
Bachelor's degree in Engineering, Life Sciences, Chemistry, or related field (Master's preferred). 10+ years of progressive quality leadership experience in a GMP/Manufacturing setting. Demonstrated experience managing regulatory compliance and quality systems (e.g., ISO 9001). Proven leadership and change management skills with cross-functional teams in multi-site environments. Certified Quality Auditor (CQA), Six Sigma, or similar certifications are a plus. Strong analytical, communication, and problem-solving skills. What's on Offer
Competitive Base Salary Bonus Potential Strategic Ownership of Quality Organization Competitive Benefits including 401k Company Match