Qureos Mentor

United Pharma Technologies Inc

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 Job Title: Quality Engineer &ndash; Medical Device Industry
 
 
 
 
 Location:
 
 Illinois, USA
 
 
 
 Job Type:
 
 Long-Term Contract
 
 
 
 
 
 
 
 Job Summary
 
 
 
 We are seeking a motivated and detail-oriented Quality Engineer to support quality assurance and compliance activities within a medical device manufacturing environment in Illinois. This opportunity is ideal for recent graduates or early-career professionals looking to gain hands-on experience in a highly regulated industry. The Quality Engineer will assist with quality systems, investigations, documentation review, and process improvement initiatives to ensure compliance with FDA and ISO standards.
 
 
 
 
 
 
 Key Responsibilities
 
 
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 Support quality assurance activities for medical device manufacturing operations.
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 Assist with non-conformance reports (NCRs), CAPA, deviations, and investigations.
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 Review manufacturing and quality documentation for compliance and accuracy.
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 Participate in root cause analysis and corrective/preventive action implementation.
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 Support internal audits and regulatory compliance activities.
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 Assist with equipment, process, and validation documentation (IQ/OQ/PQ).
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 Collaborate with manufacturing, engineering, and operations teams to improve product quality and processes.
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 Ensure compliance with FDA regulations, GMP, and ISO 13485 standards.
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 Maintain quality records and documentation in accordance with company procedures.
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 Required Qualifications
 
 
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 Bachelor&rsquo;s degree in Engineering, Biomedical Engineering, Mechanical Engineering, Life Sciences, or related field.
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 0&ndash;2 years of experience in Quality Engineering, Quality Assurance, or manufacturing environment.
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 Basic understanding of GMP, FDA regulations, and ISO 13485 standards.
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 Strong communication, analytical, and documentation skills.
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 Proficiency with Microsoft Office applications.
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 </ul>
 
 
 
 
 
 Preferred Qualifications
 
 
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 Internship or co-op experience in medical device or pharmaceutical manufacturing.
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 Familiarity with CAPA, deviations, and validation activities.
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 Understanding of quality systems and continuous improvement methodologies.
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 Required Skills
 
 
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 Attention to detail
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 Problem-solving and analytical skills
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 Documentation and reporting
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 Team collaboration
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 Time management
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 Communication skills
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 Work Environment
 
 
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 Onsite role in a regulated medical device manufacturing facility in Illinois.
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 Opportunity to work closely with cross-functional engineering and quality teams.
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 </ul>
 
 
</div>

Quality Engineer (Medical Device)

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United Pharma Technologies Inc

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Quality Engineer (Medical Device)