Master/Sr Manufacturing Associate, Upstream, ONSITE, Fremont CA- Night Shift

Boehringer Ingelheim - Fremont, CA

Hiring: Master/Sr Manufacturing Associate, Upstream, ONSITE, Fremont CA- Night Shift Company: Boehringer Ingelheim Location: Fremont, CA Job Posted Time: 2026-09-12 13:03:53 Target Skills & Keywords : Accessibility, Manufacturing Execution Systems About the job Required Skills: •The shift for this role is: Wed - Sat, 8:00pm - 6:30am PST •Independently executes complex unit operations including, but not limited to, batching and inoculation of bioreactors, operation of bioreactors, process monitoring, and harvest operations. May contribute to equipment and process troubleshooting, as needed. Implements continuous improvement projects of low complexity in the production areas. •CIP/SIP of bioreactors, tanks, and harvest equipment •Media preparation and transfer into tanks and disposables •Daily analytics and maintenance of analytical equipment •May be required to support parts cleaning and weigh and dispense operations •Performs internal support duties including stocking consumables/materials, updating controlled SOP binders, appropriately discarding expired reagents, recognizing and reporting process and equipment anomalies •Documents work according to cGMP and cGDP Qualifications: •High school degree plus minimum four (4) year’s work experience in GMP regulated industry •Associates/Bachelor’s degree from an accredited institution or biotechnology vocational training preferred •Four (4) or more years of experience in cGMP regulated industry •Demonstrated capacity to concentrate on detail oriented work in a complex technical setup with a Quality and Right the first time mindset •Strong written and verbal communication skills •Demonstrated capacity to work with computer-based systems and ideally experience with process control systems (e.g. Delta V) and manufacturing execution systems (MES) •Demonstrated capacity to read and understand SOPs and work instructions and document work in a written format applying cGMP standards •Demonstrated capacity to work as part of a high performing team and collaborate effectively with staff •Strong working knowledge of biopharmaceutical manufacturing practices, as well as a strong understanding of biologics principles are required •Working in a highly regulated environment following all applicable BI and BI Fremont SOPs, OCPs and BGSs for cGMP, EHS and Compliance policies Compensation: •$75,000 - $122,000 / year •Flexible work environment (work from home / hybrid options) •The position may be eligible for a role specific discretionary bonus, relocation, and/or other compensation elements Interested candidates, please apply directly through the job posting on company's career page or try via AI auto apply on this platform. Don't miss this opportunity to join a forward-thinking team!