Quality Assurance Specialist
2 weeks ago
Location: Lincolnshire, IL area
Hire Type: Direct Hire
Overview:
Sterling has helped build careers for thousands of professionals like yourself. Our expert recruiters support you at every step in the process and as a Best of Staffing company, Sterling provides exciting work with exceptional employers across the U.S.
Job Summary:
The Quality Engineer ensures continuous quality compliance and improvement within a medical device manufacturing environment. This person will monitor ongoing manufacturing operations to ensure that quality issues are quickly addressed. Will create and maintain quality documentation, as required.
Key Responsibilities:
- Ensure compliance of customer requirements, industry standards, and safety in the workplace.
- Educate operators and production associations on quality and compliance procedures.
- Interface with customers on quality-related matters and improve incoming customer inquiries to reduce Return Material Authorizations (RMAs).
- Support customer audits.
- Understand and follow company quality policy guidelines, customer specifications, and adhere to regulatory compliance.
- Focus on eliminating scrap. Keep supervisors informed and escalate issues when needed.
- Drive Proactive Continuous Improvement on Yield & Quality Metrics by designing templates for documents, file types, and document databases.
- Drive cross-functional teams to deliver continuous improvement activities for internal processes and deliverables.
- Provide supervision and guidance to Quality Assurance Inspectors and Technicians.
- Guide Quality Assurance operators, group leaders, and technicians in ongoing quality improvement activities.
Requirements:
- Bachelor's Degree is required, preferably in an Engineering field.
- Relevant previous work experience in Quality Engineering within a manufacturing environment is required.
- Understanding and experience with manufacturing quality tools and processes (e.g., CAPA, FMEA, PPAP, etc.)
- Ability to work well in a fast-paced manufacturing environment.
- Strong ability to identify and solve problems proactively using structured problem-solving tools, including making timely and effective decisions.
- Ability to design and conduct experiments, as well as to analyze, interpret, validate, and communicate data to key stakeholders.
- Any Quality Certifications are a plus (e.g., Six Sigma, CQE, etc.).
- Experience working in a highly-regulated industry is preferred (e.g., medical device, automotive, aerospace, defense, etc.)
Equal Employment Opportunity:
Qualified applicants will receive consideration for employment without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, disability, protected veteran status, or genetic information.
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