Astrix Inc
Our client, a leading biotechnology manufacturer in the therapeutics space, is seeking a QC Specialist with strong LIMS expertise to drive analytical testing, ensure data integrity, and advance digital lab process improvements.
Title: QC Specialist - Biotechnology Pay: $45-52/hr Location: Redwood City, CA Contract to hire
We are seeking a
QC Specialist
with strong
LIMS expertise
to support analytical testing, data integrity, and digital lab process improvements in a biotechnology environment. This role will ensure compliance with quality standards while collaborating with Quality, Manufacturing, and R&D teams to support product release, stability testing, and process improvements.
Key Responsibilities
Perform analytical and functional QC testing of raw materials, in-process, and final product batches
Manage and review data within LIMS to ensure accuracy and traceability
Author and revise SOPs, test methods, and QC documentation in compliance with cGMP / ISO standards
Support OOS investigations, deviations, and change control activities in collaboration with QA
Assist with equipment calibration, troubleshooting, and maintenance
Contribute to method qualifications, process validation, and audit readiness Qualifications
Bachelor's degree in Biology, Chemistry, Biochemistry, or related field
2-4+ years of QC experience in biotech, pharma, or biomanufacturing
Hands-on experience with LIMS and strong knowledge of GMP/GLP/ISO standards Preferred
Experience with HPLC, ELISA, PCR, spectrophotometry, or enzymatic assays
Familiarity with ERP/ELN systems and digital documentation tools
Background in enzyme, protein, or biologics manufacturing
INDBH
Title: QC Specialist - Biotechnology Pay: $45-52/hr Location: Redwood City, CA Contract to hire
We are seeking a
QC Specialist
with strong
LIMS expertise
to support analytical testing, data integrity, and digital lab process improvements in a biotechnology environment. This role will ensure compliance with quality standards while collaborating with Quality, Manufacturing, and R&D teams to support product release, stability testing, and process improvements.
Key Responsibilities
Perform analytical and functional QC testing of raw materials, in-process, and final product batches
Manage and review data within LIMS to ensure accuracy and traceability
Author and revise SOPs, test methods, and QC documentation in compliance with cGMP / ISO standards
Support OOS investigations, deviations, and change control activities in collaboration with QA
Assist with equipment calibration, troubleshooting, and maintenance
Contribute to method qualifications, process validation, and audit readiness Qualifications
Bachelor's degree in Biology, Chemistry, Biochemistry, or related field
2-4+ years of QC experience in biotech, pharma, or biomanufacturing
Hands-on experience with LIMS and strong knowledge of GMP/GLP/ISO standards Preferred
Experience with HPLC, ELISA, PCR, spectrophotometry, or enzymatic assays
Familiarity with ERP/ELN systems and digital documentation tools
Background in enzyme, protein, or biologics manufacturing
INDBH