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

• 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.

• 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.