Quality Systems Specialist
Listed on 2026-07-01
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Quality Assurance - QA/QC
Quality Control - QC Analysts/Managers, Production QC/QA, QA Specialist - Analyst/Manager, Regulatory Compliance Specialist
Quality Systems Specialist I
Kelly Engineering is seeking a Quality Systems Specialist I to support a leading organization within the life sciences and diagnostic manufacturing industry.
Responsibilities:
• Review manufacturing and batch records for completeness and compliance
• Verify documentation accuracy, signatures, dates, and required approvals
• Support quality systems and document control activities
• Organize and archive quality documentation in accordance with company procedures
• Maintain accurate records and filing systems
• Follow SOPs and quality procedures
• Assist with records retention and document management activities
• Collaborate with Quality team members to support compliance initiatives
Requirements:
• High School Diploma or equivalent required
• Minimum 2 years of experience in a manufacturing environment
• Strong attention to detail
• Proficiency with Microsoft Excel
• Strong organizational and communication skills
• Ability to work onsite in Bothell, WA
Preferred Qualifications:
• Medical device experience
• Biotechnology or pharmaceutical manufacturing experience
• Quality Systems experience
• Document Control experience
• Batch record review experience
• GMP-regulated manufacturing experience
• Experience following SOPs and quality procedures
This position offers valuable exposure to quality systems, compliance processes, and regulated manufacturing environments.
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