Manufacturing Manager
Listed on 2026-08-05
-
Manufacturing / Production
Pharmaceutical Manufacturing, Manufacturing & Industrial Operations, Validation Engineer
Position Summary
OPM Biosciences is establishing a new GMP-aligned manufacturing facility in the U.S. We are seeking a Manufacturing / Media Production Manager to build and lead cell culture media manufacturing operations from the ground up.
This role is responsible for GMP-compliant manufacturing execution, process setup, and scale-up of cell culture media production, ensuring robust, reproducible, and high-quality output.
Key ResponsibilitiesLead GMP manufacturing operations for cell culture media, including mixing, formulation, sterile filtration, and dispensing
Develop and execute SOPs, batch manufacturing records (BMRs), and GMP production workflows
Support technology transfer from R&D to manufacturing and scale-up activities
Ensure compliance with GMP requirements, batch documentation standards, and data integrity principles (ALCOA )
Manage deviations, CAPA, and change control processes in collaboration with QA/QC
Oversee production equipment operation, qualification, and maintenance support
Build, train, and develop the production team while driving operational excellence initiatives
QualificationsBachelor’s or Master’s degree in Biotechnology, Biochemical Engineering, Chemical Engineering, Pharmaceutical Sciences, or related field
5-10 years of experience in GMP manufacturing, biopharmaceutical production, or cell culture media manufacturing
Hands-on experience in aseptic processing, sterile filtration, or media formulation at production scale
Strong knowledge of GMP systems, batch documentation, and regulatory expectations (FDA/EMA preferred)
Proven experience in deviation investigation and CAPA execution
Preferred ExperienceExperience in greenfield GMP facility startup or major facility expansion
Background in cell culture media, upstream bioprocessing, or biopharma raw material manufacturing
Familiarity with single-use technologies and closed-system processing
Experience in cross-functional tech transfer (R&D to Manufacturing to QA)
Lean / Six Sigma certification is a plus
Working Conditions /Physical Requirements
Ability to stand, walk, and move materials throughout warehouse and laboratory support areas on a daily basis
Ability to occasionally lift up to 35 lbs
Ability to support early or late manufacturing schedules when required
Equal Opportunity EmployerWe are an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, or any other characteristic protected by applicable law.
NoteThis job description is intended to describe the general scope of the role. Responsibilities may evolve as the Pleasanton site ramps and organizational needs change.
#J-18808-Ljbffr(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).