Quality Compliance Manager

Quality Compliance Manager at Flextronics International USA, Inc Quality Compliance Manager at Flextronics International USA, Inc in Buffalo Grove, Illinois Posted in 5 days ago.

Type:

Full-Time Job Description:

Job Posting Start Date 04-23-2026 Job Posting End Date 07-06-2026 Flex is the diversified manufacturing partner of choice that helps market-leading brands design, build and deliver innovative products that improve the world. A career at Flex offers the opportunity to make a difference and invest in your growth in a respectful, inclusive, and collaborative environment. If you are excited about a role but don't meet every bullet point, we encourage you to apply and join us to create the extraordinary. Job Summary The Quality Compliance Manager will be based in Buffalo Grove, IL , reporting to Sr. Quality Manager . The Quality Compliance Manager will be responsible for leading and maintaining a compliant analytical laboratory that supports medical device manufacturing, product release, validation, and laboratory investigations. This role ensures laboratory operations meet FDA Quality Management System Regulation (21 CFR Part 820), ISO 13485:2016, and applicable international regulatory requirements. The manager provides technical and people leadership, ensures data integrity, and drives continuous improvement while always maintaining inspection readiness. What a typical day looks like: Laboratory Leadership & Operations Lead day‑to‑day analytical laboratory operations supporting incoming inspection, in‑process controls, final product release, validation, and complaint investigations Ensure analytical testing is accurate, timely, and aligned with product and regulatory requirements Review and approve analytical test results, reports, and data packages prior to product disposition Establish priorities and resource allocation to support production and quality needs Regulatory Compliance & Quality Systems Ensure laboratory compliance with

FDA QMSR

(21 CFR 820) , ISO 13485 , and applicable ISO testing standards Author, review, approve, and maintain laboratory SOPs, work instructions, test methods, and validation protocols Maintain inspection readiness and support FDA, notified body, customer, and internal audits Lead or support laboratory investigations including OOS/OOT, nonconformances, deviations, CAPAs, and change controls Ensure ALCOA+ data integrity principles are implemented and sustained within the laboratory Analytical Methods & Equipment Oversee development, validation, verification, and lifecycle management of analytical methods Ensure laboratory equipment is properly qualified, calibrated, maintained, and documented Manage equipment obsolescence, upgrades, and new technology introduction Evaluate and select external test laboratories when internal testing is not available People Management & Development Directly manage laboratory analysts, technicians, and/or supervisors Ensure personnel training, qualification, and competency assessments are completed and maintained Mentor staff on technical skills, GMP compliance, documentation, and root cause analysis Promote a culture of accountability, quality, and continuous improvement Safety & Environmental Compliance Ensure laboratory compliance with EHS requirements, chemical hygiene plans, and waste disposal regulations Promote safe laboratory practices and respond to safety incidents or near misses Continuous Improvement & Cross‑Functional Support Drive continuous improvement initiatives to enhance laboratory efficiency, compliance, and cost effectiveness Partner with Manufacturing, Engineering, Supplier Quality, R D, and Regulatory Affairs to resolve quality and technical issues Support process validation, design verification/validation (DV/PV), and technology transfers The experience we're looking to add to our team: Bachelor's degree in chemistry, Analytical Chemistry, Materials Science, Engineering, or related scientific discipline Minimum 7+ years of analytical laboratory experience in a regulated medical device or life sciences environment At least 2 years of people leadership or technical leadership experience Strong working knowledge of analytical techniques such as

HPLC, GC, FTIR, UV

‑Vis and wet chemistry Solid understanding of

FDA QSR, ISO

13485, and medical device quality systems Experience with Laboratory Information Management Systems (LIMS) (preferred) Six Sigma, Lean, or formal root cause analysis training (preferred) What you'll receive for the great work you provide: Full range of medical, dental, and vision plans Life Insurance Short-term and Long-term Disability Matching 401(k) Contributions Vacation and Paid Sick Time Tuition Reimbursement Pay Range (Applicable to Illinois) $136,200.00 USD - $187,300.00 USD Annual Job Category Quality Is Sponsorship Available? No Flex is an Equal Opportunity Employer and employment selection decisions are based on merit, qualifications, and abilities. We do not discriminate based on: age, race, religion, color, sex, national origin, marital status, sexual orientation, gender identity, veteran status, disability, pregnancy status, or any other status protected by law. We're happy to provide reasonable accommodations to those with a disability for assistance in the application process. Please email accessibility@flex.com and we'll discuss your specific situation and next steps (

NOTE:

this email does not accept or consider resumes or applications. This is only for disability assistance. To be considered for a position at Flex, you must complete the application process first).