QC Inspector
Experis, Temecula, CA, United States
Job Title:
Inspector, QC
Location:
Temecula, CA
Mode:
Long term Contract - 100% Onsite
Pay Range:
$20/hr to $24/hr on W2
What’s the Job?
Perform comprehensive quality assurance reviews of documentation and production activities to verify accuracy and compliance.
Audit materials, components, and line activities through visual checks, sampling, and system verification.
Support reduction of documentation and process errors by thorough review and timely escalation of issues.
Provide daily line support to ensure correct labeling, traceability, and documentation practices during relabeling and addendum operations.
Assist Engineering with technical evaluations, testing, and documentation updates to support continuous improvement initiatives.
What’s Needed?
Strong attention to detail with the ability to perform accurate and compliant documentation reviews in a regulated environment.
Working knowledge of SAP, LHR/eLHR systems, and document control practices.
Ability to understand and apply procedures, material specifications, drawings, and regulatory standards.
Effective communication skills to convey findings and collaborate with cross‑functional teams.
Familiarity with medical device regulatory frameworks such as ISO 13485 and 21 CFR 820 preferred.
Benefits (upon completion of waiting period)
Medical and Prescription Drug Plans
Dental Plan
Vision Plan
Health Savings Account
Health Flexible Spending Account
Dependent Care Flexible Spending Account
Supplemental Life Insurance
Short Term and Long Term Disability Insurance
Business Travel Insurance
401(k), Plus Match
Weekly Pay
If this is a role that interests you and you'd like to learn more, click apply now and a recruiter will be in touch with you to discuss this great opportunity. We look forward to speaking with you!
#J-18808-Ljbffr
Inspector, QC
Location:
Temecula, CA
Mode:
Long term Contract - 100% Onsite
Pay Range:
$20/hr to $24/hr on W2
What’s the Job?
Perform comprehensive quality assurance reviews of documentation and production activities to verify accuracy and compliance.
Audit materials, components, and line activities through visual checks, sampling, and system verification.
Support reduction of documentation and process errors by thorough review and timely escalation of issues.
Provide daily line support to ensure correct labeling, traceability, and documentation practices during relabeling and addendum operations.
Assist Engineering with technical evaluations, testing, and documentation updates to support continuous improvement initiatives.
What’s Needed?
Strong attention to detail with the ability to perform accurate and compliant documentation reviews in a regulated environment.
Working knowledge of SAP, LHR/eLHR systems, and document control practices.
Ability to understand and apply procedures, material specifications, drawings, and regulatory standards.
Effective communication skills to convey findings and collaborate with cross‑functional teams.
Familiarity with medical device regulatory frameworks such as ISO 13485 and 21 CFR 820 preferred.
Benefits (upon completion of waiting period)
Medical and Prescription Drug Plans
Dental Plan
Vision Plan
Health Savings Account
Health Flexible Spending Account
Dependent Care Flexible Spending Account
Supplemental Life Insurance
Short Term and Long Term Disability Insurance
Business Travel Insurance
401(k), Plus Match
Weekly Pay
If this is a role that interests you and you'd like to learn more, click apply now and a recruiter will be in touch with you to discuss this great opportunity. We look forward to speaking with you!
#J-18808-Ljbffr