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Field Applications Specialist

Job in California, Moniteau County, Missouri, 65018, USA
Listing for: Jobtailor
Full Time position
Listed on 2026-09-05
Job specializations:
  • Engineering
    Validation Engineer, Process Engineer, Quality Engineering, Pharma Engineer
Salary/Wage Range or Industry Benchmark: 95000 - 125000 USD Yearly USD 95000.00 125000.00 YEAR
Job Description & How to Apply Below
Location: California

  • Support biopharmaceutical and biotech customers across Europe to understand their process requirements
  • Design and support implementation of single-use systems used in biopharmaceutical manufacturing
  • Provide on-site and remote technical support, training, and troubleshooting
  • Act as the key technical link between customers, sales, and internal engineering teams
  • Lead technical discussions, presentations, and solution development activities
  • Support successful deployment of Meissner technologies in regulated manufacturing environments
  • Ensure solutions align with cGMP requirements and relevant FDA regulatory expectations
  • Support compliant application of technologies in pharmaceutical production environments
  • Share customer insights with global engineering and commercial teams
  • Contribute to continuous improvement of products, tools, and processes
  • Develop toward becoming a Subject Matter Expert in bioprocessing applications
Requirements
  • Bachelor's degree (B.S.) in Mechanical Engineering, Biomedical Engineering, Chemical Engineering, Manufacturing Engineering, Industrial Engineering, Industrial Technology or equivalent technical discipline from four-year college or university
  • At least one year of experience as a technical specialist in single-use systems and technologies geared toward the pharmaceutical industry
  • Proven ability to work independently
  • Strong self-motivation and time management skills
  • Travel to client facilities and Meissner entities globally may account for up to 40% of time
  • Must be a U.S. citizen, lawful permanent resident of the U.S., protected individual as defined by 8 U.S.C. 1324b(a)(3), or eligible to obtain required U.S. government authorizations to access export-regulated information
Core Competencies

Demonstrates expertise in single-use systems and bioprocessing applications within regulated pharmaceutical environments, ensuring compliance with cGMP and FDA standards while providing technical support and training to clients.

Highest-signal resume keywords
  • Single-Use Systems
  • CGMP Compliance
  • Technical Support
  • Biopharmaceutical Manufacturing
  • Regulatory Requirements
ATS Optimization Keywords Hard Skills
  • Mechanical Engineering
  • Biomedical Engineering
  • Chemical Engineering
  • Manufacturing Engineering
  • Industrial Engineering
  • Technical Specialist Experience
  • Process Requirements Analysis
  • Solution Development
  • Troubleshooting
  • Continuous Improvement
Soft Skills
  • Self-Motivation
  • Time Management
  • Independent Work
Industry Keywords
  • Biopharmaceutical
  • Biotech
  • FDA Regulatory Expectations
  • Pharmaceutical Production
  • Subject Matter Expert
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