Skip to main content
Tallo logoTallo logo
Apply for this opportunity

This job application is on an outside website. Be sure to review the job posting there to verify it's the same.

Apply Offsite

QC Lab Associate

Job

Astrix Technology Group

Newark, CA (In Person)

$61,360 Salary, Full-Time

Posted 3 days ago (Updated 1 day ago) • Actively hiring

Expires 8/4/2026

Review key factors to help you decide if the role fits your goals.
How is this calculated?
Pay Growth
?
out of 5
Not enough data
Not enough info to score pay or growth
Job Security
?
out of 5
Not enough data
Calculating job security score...
Total Score
52
out of 100
Average of individual scores

Were these scores useful?

Skill Insights

Compare your current skills to what this opportunity needs—we'll show you what you already have and what could strengthen your application.

Job Description

QC Lab Associate Astrix Technology Group - 3.4 Newark, CA Job Details Contract $28 - $31 an hour 3 hours ago Qualifications Computer operation Microsoft Outlook GMP High school diploma or GED Full Job Description QC Lab Associate About the
Opportunity:
Our client, a clinical-stage biotechnology company focused on innovative cell therapy development, is seeking a QC Lab Associate to support essential laboratory operations. This is a great opportunity for someone early in their laboratory career to gain hands-on experience within a GMP-regulated biotech/pharma environment.
Location :
Newark, CA (on-site) | 1-year contract |
Shift :
M-F 9-5 |
Compensation :
$28-31/hour
Responsibilities:
Order laboratory reagents, consumables, and office supplies in SAP; restock workstation consumables; organize reagents by expiration date using a first-in, first-out approach. Maintain cleanliness of laboratory equipment and perform daily, monthly, semi-annual, and annual cleaning activities as needed. Assist with receipt and documentation of incoming samples, reagents, and chemicals. Perform laboratory activities in accordance with applicable SOPs and cGMP requirements. Follow good documentation practices when recording activities in laboratory equipment logbooks. Handle liquid nitrogen-frozen samples and chemicals as needed. ]Support archival of Quality Control data, including preparing binders and scanning documents. Review test method data and supporting documentation as needed. Perform equipment maintenance testing as needed.
Requirements:
Minimum 1-2 years of laboratory experience Knowledge of GMP Good communication skills QC experience is a plus Basic computer skills (Word, Excel, Outlook) High School Diploma or GED required; some college or degree preferred Biotech/pharma industry background preferred This job description is a complete list of all desired skills, but not all are required. We strongly encourage candidates who have some of the skills to apply. We look forward to a conversation to learn more about you! #INDBH #LI-DNI