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Skip to job details? Hercules, CA ? $37/hour ? Monday - Friday | 8:00 AM - 5:00 PM Make Quality Count Our client, a recognized leader in the healthcare and manufacturing industry, is looking for a QC Specialist I to join their growing Quality Control team. This is an exciting opportunity for a recent graduate or early-career professional who is passionate about quality, compliance, and making a meaningful impact in a highly regulated environment. If you thrive on accuracy, collaboration, and continuous improvement, we'd love to hear from you. What You'll Do As a QC Specialist I, you'll play a key role in ensuring materials and processes meet the highest quality standards by: ✅ Performing incoming raw material inspections and reviewing Certificates of Analysis (CoA) and Certificates of Conformance (CoC) ✅ Managing QC sample pulls and retention samples while maintaining accurate documentation and storage records ✅ Creating, maintaining, and distributing Certificates of Analysis to support operational and regulatory requirements ✅ Partnering closely with Manufacturing, Warehouse, Receiving, MSAT, Planning, and QC teams to resolve issues and keep materials moving efficiently ✅ Recording inspection results and quality data in SAP and other systems with a high level of accuracy and compliance •What We're Looking For•
M
ManpowerGroup
Quality Control Specialist I
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Based on California data
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What they do
A Quality Control Analyst, in the biotech and medical device industries, works in laboratories performing biological, microbiological, and chemical tests on products and materials. Responsible for calibrating equipment, inspecting products, processing and testing materials, and reporting results. May work in other production environments to monitor and improve quality and efficiency in production systems and products.
$67,470 / year median in California
-12% projected decline
Job Description
- Quality Control Specialist I
Required Qualifications:
- + Bachelor's degree in Biology, Chemistry, Life Sciences, or a related scientific discipline + 0-2 years of laboratory, manufacturing, or quality control experience + Working knowledge of Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP) + Exceptional attention to detail and strong documentation skills + Proficiency with Microsoft Office applications
- Success in
This Role Looks Like:
- + Strong organizational and time-management skills + Effective communication and collaboration across departments + A proactive mindset with a commitment to quality and compliance + Ability to work independently while contributing to team goals
- Why You'll Love This Opportunity
- ? Gain hands-on experience in a regulated, quality-focused environment ? Work alongside industry professionals who support learning and career growth ? Participate in process improvement initiatives and cross-functional projects ? Contribute to products and processes that uphold the highest standards of safety and compliance ? Build a strong foundation for long-term career advancement
- Benefits Available Upon Eligibility
- + Medical and Prescription Drug Coverage + Dental Insurance + Supplemental Life Insurance + Short-Term Disability Insurance + 401(k) Retirement Savings Plan
- Ready to Take the Next Step?
- If you're looking to launch or grow your career in Quality Control with an industry-leading organization,
- apply today
- . We'd love to connect with you and discuss how this opportunity can support your professional goals.
About ManpowerGroup, Parent Company of:
Manpower, Experis and Talent Solutions.- _Manpower® is a global leader in contingent staffing and permanent resourcing, providing companies with strategic and operational flexibility and creating talent at scale.