Quality Manager

Comprehensive range of labware for scientific research and technical application
Excellent growth opportunity within the organization

About Our Client

My client is a global leader in precision labware, scientific glass, and life sciences packaging. With a legacy spanning over 100 years, they are committed to enabling scientific discovery and innovation through high-quality products, robust quality systems, and customer-focused solutions.

Job Description

The key responsibilities of the Quality Manager will be:

Supervise, train, and mentor quality assurance technicians and inspectors across shifts.
Monitor daily quality control activities to ensure compliance with SOPs, specifications, and regulatory guidelines
Investigate non-conformances and customer complaints; perform root cause analysis and lead corrective/preventive actions (CAPAs).
Collaborate with manufacturing, engineering, and supply chain teams to ensure quality issues are resolved effectively and timely.
Conduct internal audits and assist in customer or regulatory audits.
Analyze quality data, generate reports, and identify trends to drive continuous improvement.
Support implementation of quality system enhancements and training initiatives.
Ensure adherence to safety and environmental regulations within the QA area.

If interested, please apply using the link below. Qualified applicants will be contacted 24-48 hours upon submittal. 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

The successful Quality Manager will have:

3+ years of experience in quality assurance within a regulated manufacturing environment.
1-2 years of leadership or supervisory experience preferred.
Working knowledge of ISO standards and GMP/GLP practices.
Strong analytical, problem-solving, and organizational skills.
Proficiency with quality tools (e.g., CAPA, 8D, 5 Whys, FMEA).
Excellent communication and interpersonal skills.
Familiarity with QMS software and MS Office Suite.