Field Applications Specialist
Job in
California, Moniteau County, Missouri, 65018, USA
Listed on 2026-09-05
Listing for:
Jobtailor
Full Time
position Listed on 2026-09-05
Job specializations:
-
Engineering
Validation Engineer, Process Engineer, Quality Engineering, Pharma Engineer
Job Description & How to Apply Below
- 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
- 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
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
- Mechanical Engineering
- Biomedical Engineering
- Chemical Engineering
- Manufacturing Engineering
- Industrial Engineering
- Technical Specialist Experience
- Process Requirements Analysis
- Solution Development
- Troubleshooting
- Continuous Improvement
- Self-Motivation
- Time Management
- Independent Work
- Biopharmaceutical
- Biotech
- FDA Regulatory Expectations
- Pharmaceutical Production
- Subject Matter Expert
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