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Job Requirements of Quality Engineer:
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Employment Type:
Contractor
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Location:
Cortland, NY (Onsite)
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Quality Engineer
Job Title: Quality Engineer
Location: Onsite Cortland, NY 13045
Duration: 3-month contract (W2) with high potential for extension based on performance and business needs
Pay: $53.33/hour (W2)
Job Summary:
We are seeking a Quality Engineer to support our client s onsite operations in Cortland, NY. This role focuses on developing, implementing, and maintaining quality engineering methodologies and systems to meet internal, customer, and regulatory requirements. The ideal candidate will bring experience in supplier quality, process control, and quality systems, preferably within the medical device industry.
Key Responsibilities:
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Develop and implement effective process control systems to support product development, qualification, and ongoing manufacturing.
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Lead efforts to implement quality assurance, process controls, and CAPA systems that meet or exceed internal and external requirements.
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Act as a leader or key team member supporting quality disciplines and decisions.
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Use systematic problem-solving methodologies to identify, prioritize, and resolve quality issues.
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Drive the development and execution of streamlined business systems to proactively address quality issues.
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Promote quality awareness and ensure compliance with all applicable requirements throughout the organization.
Quality Systems Duties:
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Build quality into all aspects of work through strict adherence to quality requirements and standards.
Supplier Quality Responsibilities:
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Improve supplier performance through implementation and review of Part Quality Plans (PQP).
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Communicate and facilitate PQP submissions and approvals for purchased products.
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Support supplier selection through qualification processes, including audits.
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Ensure supplier compliance with Quality Management System (QMS) and applicable regulatory standards.
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Manage Corrective and Preventive Action (CAPA) processes for assigned suppliers.
Required Qualifications:
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Bachelor s degree in engineering or a technical discipline (non-technical degree considered with 7+ years relevant experience).
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5+ years of experience in manufacturing, engineering design, quality assurance, or regulatory assurance.
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Strong analytical and problem-solving skills with the ability to lead and influence cross-functional teams.
Preferred Qualifications:
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ASQ Certified Quality Engineer (CQE) or Certified Quality Auditor (CQA).
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Experience with QMS tools and continuous improvement methodologies.
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Previous supplier quality experience in the medical device industry.