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Manufacturing Associate - Upstream
Job in
Fremont, Alameda County, California, 94537, USA
Listed on 2026-01-20
Listing for:
Asahi Kasei Corporation
Full Time
position Listed on 2026-01-20
Job specializations:
-
Manufacturing / Production
Operations Engineer, Manufacturing Engineer
Job Description & How to Apply Below
Bionova is a rapidly growing, biologics CDMO focused on developing and manufacturing recombinant protein products using mammalian cell culture processes. Our business success is built on bringing together top scientific talent, arming them with the best available tools, and setting them loose in an agile, energized culture focused on solving difficult client problems. Because our success depends on our ability to exceed our clients’ expectations, we look for candidates with an innate desire to serve.
Adaptability and an interest in transformative action are also common attributes among our team. Bionova became a subsidiary of Asahi Kasei Medical in May 2022, a division of Tokyo-based Asahi Kasei Group. This acquisition has enabled Bionova to greatly accelerate growth of the business, both in capacity of current service offerings and expansion into new service offerings.
** Company:
** Bionova Scientific LLC
*
* Job Description:
**** Company
Summary:
** Bionova is a rapidly growing, biologics CDMO focused on developing and manufacturing recombinant protein products using mammalian cell culture processes. Our business success is built on bringing together top scientific talent, arming them with the best available tools, and setting them loose in an agile, energized culture focused on solving difficult client problems.
Because our success depends on our ability to exceed our clients’ expectations, we look for candidates with an innate desire to serve. Adaptability and an interest in transformative action are also common attributes among our team.
*
* Position Summary:
** The
** Manufacturing Associate
** will actively contribute to the manufacturing projects at the Bionova Scientific West Warren site. As part of the Cell Culture/Manufacturing group, you will have opportunities to work on wide-ranging set of projects for troubleshooting and investigations, system and workflow implementation, and tech transfers of processes into a GMP mulit-product manufacturing facility. The role will provide hands-on execution of complex experiments in a team setting.
The role will support GMP and manufacturing activities.
*
* Essential Duties and Responsibilities:
*** Executes with oversight of qualified staff complex unit operations including but not limited to media prep; cell culture thaw, expansion, and end of production banking; operation of single-use bioreactors, process monitoring and harvest operations.
* Performs internal support activities such as maintenance of analytical equipment, stocking of consumables, discarding expired reagents, material coordination and weigh and dispense.
* Maintains own training within compliance and trains other GMP associates upon completion of trainer qualification.
* Support in equipment troubleshooting, pilot scale material generation, non-GMP tox material generation and GMP upstream manufacturing activities.
* Author/review/approve technical documents such as tech transfer protocols and reports, experimental plans, production batch records, training materials, manufacturing SOPs, and regulatory filing documents per project needs.
* Documents work according to cGMP and cGDP.
* Adheres to established regulations and follows cGMP established by site.
* Maintain cleanroom standards, practices, and housekeeping according to SOPs.
* Recognize any minor issues from the equipment and any affiliated documentation and take appropriate corrective action within scope. Notify leads/managers of issues and discrepancies immediately.
* Assess impact of issues and non-conformities to products and projects as they pertain to product safety and efficacy or project milestones.
* Evaluate new technologies and innovations to improve operational efficiency or expand cell culture capabilities.
* Contributes to quality activities such as investigations and area walk-throughs and support authoring deviations, CAPA, change control.
* Other duties as assigned to ensure appropriate compounding practices
*
* Working Conditions:
*** This position required to work in a lab/office setting. The role requires walking, standing, stooping, kneeling, and crouching. The employee must occasionally lift and or move up to 20 pounds independently.
** Qualifications
* ** Minimum of Associate degree with 1-2 years of relevant experience, or combination of experience and relevant advanced degree, preferably in biopharma manufacturing role.
* Must have bioreactor operations experience.
* Understanding of mammalian cell culture performance is required.
* Working knowledge of cGMP compliance as it pertains to procedures, processes, and manufacturing
* Experience with process monitoring software and equipment…
Position Requirements
10+ Years
work experience
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