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Astrix Technology Group

QC Associate II

Pay: $30–$35/hr

Posted: 6 weeks ago

Location: Fremont, CA (Onsite)

Last Updated: 2 weeks ago

Hours: Full-Time

Expires: 10/1/2026

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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

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Job Description

QC Associate II Astrix Technology Group - 3.4 Fremont, CA Job Details Contract $30 - $35 an hour 17 hours ago Qualifications Bachelor's degree Full Job Description QC Associate II We are partnering with a multi-product biopharmaceutical manufacturing facility to place a QC Associate II within their Physical-Chemical Testing group. This role is well-suited to a detail-oriented analytical professional who can execute both routine and non-routine testing across bulk drug substance, finished product, and raw material matrices. The ideal candidate brings 3-5 years of relevant industry experience, hands-on analytical instrumentation skills, and a strong compliance mindset.

Type :

6-month contract |

Location :

Onsite in Fremont, CA |

Hours :

M-F 8-5 |

Compensation :

$30-$35/hr What You'll Do Independently perform a range of laboratory testing methods following appropriate qualification, including UV-Vis spectroscopy, qPCR, FTIR, and compendial test methods. Coordinate and execute routine and non-routine analytical testing in support of a multi-product facility. Maintain lab consumables and materials inventory, properly dispose of expired reagents, and flag equipment or process irregularities. Generate accurate, timely analytical results with a "right first time" approach. Document all testing activities in full compliance with cGMP and cGDP standards. Follow site-specific SOPs, quality systems, and applicable regulatory requirements. What We're Looking For Bachelor's degree in Biology, Life Sciences, or a related field required. 3-5 years of relevant industry experience. GMP experience strongly preferred. Hands-on proficiency with UV-Vis absorbance, qPCR, and FTIR preferred. Strong written and verbal communication skills. Demonstrated customer focus with the ability to collaborate across departments and organizational levels. Ability to work both independently and collaboratively to meet team and site goals. Strong attention to detail with a focus on execution accuracy. 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