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MES MBR Designer

Job in Fremont, Alameda County, California, 94537, USA
Listing for: The Fountain Group
Full Time position
Listed on 2025-12-27
Job specializations:
  • Manufacturing / Production
    Manufacturing Engineer, Quality Engineering
Salary/Wage Range or Industry Benchmark: 80 - 100 USD Hourly USD 80.00 100.00 HOUR
Job Description & How to Apply Below

Pay: $80-100/hr based on experience
Location: Hybrid; onsite in Fremont 2-3 days a week
Duration:

Description:
  • The M  designer is responsible for understanding all the complexities of the BioMES system, revising and designing new electronic batch records, troubleshooting E  issues, and leading continuous improvement initiatives relative to BioMES.
  • This position is also responsible for the overall business process and improvement topics related to electronic records.
  • This position is expected to understand the nuances of the highly complicated electronic system.
  • This position utilizes LEAN tools to systematically evaluate information flow, create project plans, and drive right first-time success.
  • The M  designer trains modelers to learn how to generate batch records, generates and refines batch record creation training materials, and troubleshoots EBRs.
  • The M  designer works with client groups (Process Engineers, Operations, Quality) to determine design changes and improvement opportunities within the scope of electronic batch records and leads the team to prioritize and implement said improvements.
  • This role is required to work with industry experts to stay abreast of industry changes and expectations related to computer systems and electronic batch record design and to influence changes to software such that it continues to meet the needs of the business.
  • The M  designer leads and participates in project teams and works within the Bio Pharma BioMES team to standardize business processes.
Skills:
  • Subject matter expert relative to manufacturing and MES Master Batch Records.
  • Ability to transform/translate process information/design from process description into a MES Master Batch Record.
  • Experience working on multiple projects simultaneously.
  • Technical writing skills.
  • Technical knowledge of manufacturing systems, methods and procedures, biopharmaceutical manufacturing processes, and knowledge of regulatory aspects (cGMP).
Education:
  • Professional training or Associates/Bachelor's degree in STEM, IT, or equivalent.
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