Responsibilities include performing and reviewing a variety assays in the Quality Control organization in support of In-Process intermediates, drug substance, drug product and stability sample testing in a cGMP environment.

Specifically, biochemical assays, using analytical techniques and instrumentation, such as high performance liquid chromatography (HPLC) and mass spectroscopy. The QC Technician must be able to interpret data troubleshoot assay failures and equipment issues while adhering to strict guidelines on cGMP documentation. In addition, the individual will support cycle development, performance qualifications, method transfers, discrepancy/out of specification investigations and collaborate with external groups to identify improvement opportunities in technology and business process

Shift: Monday to Thursday or Tuesday to Friday, 4×10’s

Day: 6:00am to 4:30pm

Swing 1:30pm to 12:00am

Contract duration:  12 months with possible extension up to 3 years

Important: Genentech has mandated COVID-19 vaccination for their workforce, effective October 1, 2021. All external personnel providing services to Genentech are required to comply with this requirement.

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