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MP
Michael Page
Regulatory and Quality Specialist - Labware - Millville, NJ
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What they do
A Quality Assurance Specialist specializes in the prevention of faults in manufactured products and solutions.
$69,280 / year median in New Jersey
+1% projected growth
Job Description
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 & Regulatory Specialist will be: Support the maintenance and continuous improvement of the Quality Management System (QMS). Ensure compliance with applicable quality, regulatory, and industry standards, including ISO requirements and Good Manufacturing Practices (GMP), as applicable. Review, create, and maintain quality and regulatory documentation, including procedures, work instructions, specifications, and records. Coordinate document control activities and ensure accurate record retention. Assist with internal, customer, and third-party audits, including preparation, execution, and follow-up of corrective actions. Investigate quality issues, nonconformances, complaints, and deviations; support root cause analysis and corrective/preventive action (CAPA) implementation. Monitor quality metrics and prepare reports to support management review and continuous improvement efforts. Review change controls and assess potential quality and regulatory impacts. Support supplier qualification activities and participate in supplier quality evaluations. Assist with product certifications, declarations of conformity, and customer regulatory inquiries. Collaborate with Manufacturing, Engineering, Operations, and Customer Service teams to resolve quality and compliance-related issues. Participate in risk assessments and validation activities as required. Stay current with evolving regulatory requirements and industry best practices. 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 & Regulatory Specialist will have: Bachelor's degree in Quality Assurance, Chemistry, Biology, Engineering, Regulatory Affairs, or a related scientific discipline. Relevant work experience will also be considered. 1-5 years of experience in quality assurance, regulatory affairs, manufacturing quality, or a related role. Knowledge of Quality Management Systems and relevant ISO standards. Experience with CAPA, root cause analysis, audits, and document control processes. Strong understanding of regulatory compliance requirements within manufacturing, laboratory, medical device, pharmaceutical, or life sciences environments. What's on Offer My client can offer the following for the