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Manufacturing Manager

Job in Pleasanton, Alameda County, California, 94566, USA
Listing for: OPM Biosciences
Full Time position
Listed on 2026-08-05
Job specializations:
  • Manufacturing / Production
    Pharmaceutical Manufacturing, Manufacturing & Industrial Operations, Validation Engineer
Salary/Wage Range or Industry Benchmark: 120000 - 180000 USD Yearly USD 120000.00 180000.00 YEAR
Job Description & How to Apply Below

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 Responsibilities

Lead 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

Qualifications

Bachelor’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 Experience

Experience 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 Employer

We 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.

Note

This job description is intended to describe the general scope of the role. Responsibilities may evolve as the Pleasanton site ramps and organizational needs change.

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