QC INSPECTOR

Manufacturing & production Qc inspector

QC INSPECTOR.

san jose, california Posted 4 days ago Closes 7/26/2026 Job details Summary Spherion $30.00 - $35.00 per hour Temporary 5:30 AM - 1:00 PM Industry manufacturing & production (Production Occupations) Reference number S_177383 Ensure product traceability is maintained through the inspection process Generate incoming inspection reports using Good Documentation Practices (GDP) and adhere to internal Record Retention policies. Initiate NCMR (Non-Conforming Material Reports) upon identification of discrepant material Work with Supplier Quality and Manufacturing to investigate and resolve nonconformities Utilize first-in-first-out methodology and be able to reprioritize inspections based on production needs ? Perform product release transactions in the ERP system and communicate with the material handling team ? Provide inspection feedback to the R D team during the development of new components and subassemblies ? Participate in Measurement System Analysis (MSA) ? Prepare quality documentation and reports by collecting, analyzing, and summarizing information and trends regarding inspection results ? Maintain trained status for, and comply with, all relevant aspects of the PROCEPT BioRobotics Quality Management System to ensure product and support regulatory compliance ? Updates job knowledge by studying trends in and developments in quality management; participating in ... educational opportunities; reading professional

Responsibilities:

nspection &

Documentation:

Perform incoming inspections and maintain meticulous product traceability; generate detailed quality reports adhering to Good Documentation Practices (GDP) and internal retention policies.

Defect Management:

Identify discrepant materials and initiate Non-Conforming Material Reports (NCMR); collaborate directly with Supplier Quality and Manufacturing to investigate and resolve nonconformities.

Workflow Optimization:

Prioritize daily inspections utilizing the first-in-first-out (FIFO) methodology, adapting quickly to changing production schedules and requirements.

System Execution & Collaboration:

Execute product release transactions within the ERP system, coordinate with the material handling team, and provide actionable inspection feedback to R D during new component development.

Continuous Improvement:

Participate in Measurement System Analysis (MSA) and summarize inspection trends to actively support and maintain compliance with the Quality Management System (QMS).

Working hours:

5:30 AM - 1:00

PM Skills:

ndustry

Experience:

Background working in a regulated medical device manufacturing environment (ISO 13485 / FDA 21 CFR Part 820 compliance).

Technical Proficiency:

Competency reading blueprints/schematics and utilizing precision measurement tools (e.g., calipers, micrometers, CMM, or optical comparators).

System Knowledge:

Familiarity with ERP systems (such as SAP, Oracle, or Arena) for inventory and product release transactions.

Problem Solving:

Foundational knowledge of root cause analysis and implementing corrective actions for non-conforming materials.

Documentation:

Track record of applying Good Documentation Practices (GDP) within a fast-paced production setting

Education:

No Degree Required Experience:

1-4 years

Qualifications:

Inspection Competency:

Ability to interpret engineering drawings, blueprints, and technical specifications to perform accurate dimensional and visual inspections.

Equipment Operation:

Proficiency in operating standard inspection tools, including calipers, micrometers, height gauges, and thread gauges.

Documentation Literacy:

Accuracy in recording inspection data, completing logs, and processing quality records in alignment with standard operating procedures.

Computer Skills:

Basic proficiency with computer systems, including data entry into inventory, ERP, or quality databases and using standard office software. Attention to

Detail:

Precision in identifying component defects, surface flaws, and deviations fro Spherion has helped thousands of people just like you find work happiness! Our experienced staff will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. Whether you're looking for temporary, temp-to-perm or direct hire opportunities, no one works harder for you than Spherion.

Equal Opportunity Employer:

Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. At Spherion, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact Callcenter@spherion.com. Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Spherion offers a comprehensive benefits package, including: medical, prescription, dental, vision, AD&D, and life insurance offerings, short-term disability, and a 401K plan (all benefits are based on eligibility). Qualified applicants in San Francisco with criminal histories will be considered for employment in accordance with the San Francisco Fair Chance Ordinance. Qualified applicants with arrest or conviction records will be considered for employment in accordance with the Los Angeles County Fair Chance Ordinance for Employers and the California Fair Chance Act. We will consider for employment all qualified Applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles' Fair Chance Initiative for Hiring Ordinance. Show more key responsibilities nspection &

Documentation:

Perform incoming inspections and maintain meticulous product traceability; generate detailed quality reports adhering to Good Documentation Practices (GDP) and internal retention policies.

Defect Management:

Identify discrepant materials and initiate Non-Conforming Material Reports (NCMR); collaborate directly with Supplier Quality and Manufacturing to investigate and resolve nonconformities.

Workflow Optimization:

Prioritize daily inspections utilizing the first-in-first-out (FIFO) methodology, adapting quickly to changing production schedules and requirements.

System Execution & Collaboration:

Execute product release transactions within the ERP system, coordinate with the material handling team, and provide actionable inspection feedback to R D during new component development.

Continuous Improvement:

Participate in Measurement System Analysis (MSA) and summarize inspection trends to actively support and maintain compliance with the Quality Management System (QMS). experience 1-4 years skills ndustry

Experience:

Background working in a regulated medical device manufacturing environment (ISO 13485 / FDA 21 CFR Part 820 compliance).

Technical Proficiency:

Competency reading blueprints/schematics and utilizing precision measurement tools (e.g., calipers, micrometers, CMM, or optical comparators).

System Knowledge:

Familiarity with ERP systems (such as SAP, Oracle, or Arena) for inventory and product release transactions.

Problem Solving:

Foundational knowledge of root cause analysis and implementing corrective actions for non-conforming materials.

Documentation:

Track record of applying Good Documentation Practices (GDP) within a fast-paced production setting qualifications

Inspection Competency:

Ability to interpret engineering drawings, blueprints, and technical specifications to perform accurate dimensional and visual inspections.

Equipment Operation:

Proficiency in operating standard inspection tools, including calipers, micrometers, height gauges, and thread gauges.

Documentation Literacy:

Accuracy in recording inspection data, completing logs, and processing quality records in alignment with standard operating procedures.

Computer Skills:

Basic proficiency with computer systems, including data entry into inventory, ERP, or quality databases and using standard office software.

Attention to

Detail:

Precision in identifying component defects, surface flaws, and deviations from established quality standards education No Degree Required share this job. send via e-mail print it Get in touch. We are here to help you with your questions. AD Arceo, Daryl darylarceo@spherion.com