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Manufacturing
Quality Control Analyst
Alameda, CA
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Spectraforce

QC Specialist

Job Description

Job Title:
QC Specialist Location:
Alameda, CA Contract Duration:
Work Arrangement:
Onsite Position Overview Our client, a medical device organization, is seeking a hands-on QA Technician to support daily quality assurance activities at its Alameda manufacturing facility. This role supports manufacturing cleanrooms and production lines through in-process product inspections, incoming component inspections, and documentation reviews. The technician will also assist with supplier qualification and equipment qualification activities as needed. The selected candidate will help ensure that manufactured products, supplier components, and production records meet established quality requirements. The role may require supporting two production lines based on time-sensitive production needs, workload priorities, or team absences. Key Responsibilities Quality Inspection & Manufacturing Support Perform in-process inspections and product quality checks on manufacturing production lines. Inspect incoming supplier parts and components against established specifications and quality requirements. Provide hands-on quality support across cleanroom manufacturing environments and production lines. Support quality activities across multiple production lines as operational needs change. Documentation & Quality Records Review manufacturing records and inspection documentation for accuracy, completeness, and compliance with established requirements. Maintain accurate quality documentation and inspection records. Help verify that products and manufacturing records meet applicable quality standards. Supplier & Equipment Qualification Support supplier qualification activities and maintain related quality documentation. Assist with new equipment qualification activities as needed. Collaborate with manufacturing and quality teams to support daily production requirements. Required Qualifications & Experience Junior-to-mid-level experience in medical device manufacturing quality assurance. Candidates with fewer than four years of relevant experience may be considered. Hands-on experience working in cleanroom manufacturing environments. Familiarity with in-process inspections and incoming quality inspections. Experience reviewing manufacturing documentation and inspection records. Strong attention to detail and ability to identify quality or documentation discrepancies. Ability to work onsite at the Alameda manufacturing facility. Flexibility to support changing production priorities and multiple manufacturing lines. Preferred Qualifications Experience in supplier quality or supplier qualification activities. Familiarity with document control and quality record management. Experience supporting equipment qualification. Previous experience in a startup or fast-paced medical device manufacturing environment. Ideal Candidate Profile The ideal candidate is a hands-on quality technician with experience supporting medical device manufacturing operations, particularly in cleanroom environments. They should be comfortable performing production-line inspections, checking incoming components, reviewing manufacturing records, and adapting to changing production priorities. Candidates with exposure to supplier quality, equipment qualification, or documentation control would be especially valuable.
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