Part-Time Quality Control Specialist

ZipRecruiter; Sunnyvale (CA); On-site; USD 40,000 - 60,000; Part time

Job summary

A leading recruiting enterprise seeks a QC Technical Specialist to join their Quality team in California. The position involves conducting critical inspections of medical devices, ensuring compliance with strict regulatory standards, and working closely with engineering to enhance product quality. Candidates should possess significant experience in quality control, inspection skills, and a relevant associate degree. This part-time role offers flexibility and the potential for future contracts.

Qualifications

• Minimum of 8 years of experience in medical device quality control.
• Strong understanding of QSR, ISO 13485, and GMP/GDP compliance.
• Ability to read and interpret engineering drawings and product specifications.

Responsibilities

• Perform visual, dimensional, and functional inspections of components.
• Draft and revise inspection and quality-related work instructions.
• Document and investigate non-conformances.

Skills

Inspection Skills

Regulatory Compliance

Organizational Skills

Communication Skills

Education

Associate degree in Mechanical, Industrial, Electrical Engineering

Tools

Calipers

Micrometers

Optical Comparators

MS Excel

Job description

Job Title: QC Technical Specialist

Location: San Jose, CA

Employment Type: Part-Time (Hours to be determined)

6 Month Contract Position with potential extensions

Job Overview:

We are seeking a highly motivated and detail-oriented QC Technical Specialist to join our Quality team. This role supports manufacturing and engineering by inspecting raw materials, in-process subassemblies, and finished products. The ideal candidate will bring strong inspection skills, regulatory compliance experience, and the ability to work in a fast-paced environment.

Key Responsibilities:

• Perform visual, dimensional, and functional inspections of components and finished products using various tools (calipers, micrometers, optical comparators, etc.).
• Conduct inspections across all QC areas: incoming (IQC), in-process, and final.
• Draft and revise inspection and quality-related work instructions to meet regulatory and internal standards.
• Review documentation such as LHRs, DHRs, and sterilization records for accuracy and compliance with GDP.
• Document and investigate non-conformances, ensuring timely resolution.
• Manage calibration and maintenance schedules for inspection equipment.
• Support cleanroom environmental monitoring and data reviews.
• Collaborate with engineering teams to improve inspection processes and product quality.
• Train and support new QC Technicians as needed.

Qualifications:

• Associate degree in Mechanical, Industrial, Electrical Engineering, or related technical field.
• Minimum of 8 years of experience in medical device quality control.
• Strong understanding of QSR, ISO 13485, and GMP/GDP compliance.
• Ability to read and interpret engineering drawings and product specifications.
• Proficient in using inspection and measurement tools and equipment.
• Basic computer skills, including MS Excel; experience with eQMS/ePLM systems is a plus.
• Excellent communication and interpersonal skills.
• Self-starter with strong organizational skills and the ability to work independently.

Company Description: We're a recruiting and staffing enterprise that blends the resources of the world's largest talent company with the local insights of our independent franchise owners. A pioneer in the staffing industry, we’ve been providing companies with workforce solutions for over 75 years while helping people find jobs and build careers where they can thrive.