Quality Engineer II

JBL Resources
  • Covington, GA
  • Instant Apply
11 days ago

Job Description

Quality Engineer II
Location: Greater Atlanta Area
About Our Client:
Our client is a highly respected organization within the manufacturing industry, recognized for delivering innovative, high-quality solutions to a global customer base. They are committed to operational excellence and continuous improvement, leveraging advanced technologies to remain competitive and forward-thinking. With a collaborative, performance-driven culture, the company empowers employees to take ownership of their work while supporting professional growth and long-term career development. This is an excellent opportunity to join a stable, reputable organization that values integrity, quality, and its people.
Key Responsibilities:
  • Serving as the Quality representative on product development and process change project teams to ensure seamless collaboration and adherence to quality standards.
  • Ensuring Design Control requirements are appropriately applied to new product development and product or process changes through diligent review and implementation.
  • Supporting design transfer and product lifecycle activities by collaborating with cross-functional teams to facilitate smooth transitions and continuous improvement.
  • Creating, reviewing, and maintaining documentation required for Design History Files (DHF) to ensure accurate record-keeping and regulatory compliance.
  • Creating, reviewing, and maintaining Quality System documentation, including procedures, work instructions, and records, to uphold quality standards.
  • Developing and reviewing product documentation to support regulatory and quality requirements, ensuring clarity and compliance.
  • Generating and supporting quality documentation such as Requests for Service (RFS), Engineering Change Requests (ECR), Product Quality Reports (PQR), and related records to facilitate quality tracking and improvements.
  • Ensuring compliance with corporate, divisional, and departmental procedures through ongoing review and adherence.
  • Creating and reviewing validation documentation including Process Validation Protocols, Product Validation Protocols, Stability Protocols, Test Methods, and Validation Reports to confirm product integrity.
Qualifications:
  • Bachelor’s degree in Engineering, Technology, Science, or related field.
  • Minimum 3 years of relevant industry experience, with 2+ years supporting product development or quality engineering functions.
  • Proven expertise in Design Controls, validation, risk management, and quality systems
  • Strong technical documentation skills.
  • Knowledge of Quality Management Systems and regulatory requirements.
  • Support experience in product development programs
  • Familiarity with Design History Files (DHF), Engineering Change Requests (ECR), and product change management.
  • Experience conducting internal and supplier audits.
  • Industry-specific experience in medical devices.
  • ASQ certifications such as CQE, CQA, or CMQ/OE.
  • NO C2C CANDIDATES

Interested Candidates please apply on our website at https://jobs.jblresources.com.
For more information about our services and great opportunities at JBL Resources, please visit our website: https://www.jblresources.com.
JBL Resources is proud to have earned the reputation of being a premier provider of top talent professionals in the fields of engineering, human resources, logistics, operations, and supply chain management. As specialists in both permanent placement and contract services, our mission is to help companies and individuals become all they were created to be.
**JBL is an Equal Opportunity Employer and E-Verify Company

Numbers & Facts

LocationCovington, GA

Skills

  • American Society for Quality (ASQ)unmatched
  • Certified Quality Engineer (CQE)unmatched
  • Change Managementunmatched
  • Continuous Improvementunmatched
  • Corporate Complianceunmatched
  • Cross-Functionalunmatched
  • Documentationunmatched
  • Engineering Change Orderunmatched
  • Human Resourcesunmatched
  • Internal Auditunmatched
  • Logisticsunmatched
  • Maintain Complianceunmatched
  • Manufacturingunmatched
  • Medical Equipmentunmatched
  • Process Validationunmatched
  • Product Designunmatched
  • Product Developmentunmatched
  • Product Documentationunmatched
  • Product Lifecycleunmatched
  • Product Managementunmatched
  • Product Reviewsunmatched
  • Product Supportunmatched
  • Product Testingunmatched
  • Quality Assurance Methodologyunmatched
  • Quality Engineeringunmatched
  • Quality Managementunmatched
  • Quality Metricsunmatched
  • Record Keepingunmatched
  • Regulationsunmatched
  • Regulatory Complianceunmatched
  • Regulatory Requirementsunmatched
  • Risk Managementunmatched
  • Supply Chain Managementunmatched
  • Supply Chain Operationsunmatched
  • Support Documentationunmatched
  • Systems Maintenanceunmatched
  • Team Playerunmatched
  • Technical Writingunmatched
  • Validation Documentationunmatched
  • Validation Planunmatched
  • Validation Testingunmatched
  • Vendor/Supplier Evaluationunmatched

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