Automation Engineer
Listed on 2025-12-22
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Engineering
Quality Engineering, Process Engineer, Biomedical Engineer, Manufacturing Engineer
Job Description
JVM Global is a consulting partner to regulated life sciences companies—bringing deep technical, validation, and quality expertise to every stage of the product lifecycle. We help pharmaceutical, biotech, and medical device organizations overcome complexity, accelerate timelines, and stay audit-ready.
We are currently seeking to identify Automation Engineers for both immediate and anticipated project needs. While there may not be an immediate vacancy, we encourage you to apply if you meet the qualifications. Qualified applicants will be contacted as relevant projects arise.
Role Requirements- This is a U.S. based role requiring 25–75% travel, depending on project location and client needs
- Flexibility for on-site client work is essential
- Candidates may reside anywhere in the United States but must be authorized to work for any U.S. employer without the need for visa sponsorship.
- Bachelor’s degree in engineering or equivalent experience
- Life sciences industry experience preferred (pharma, biotech, or medical device)
- Knowledge of 21 CFR Part 11, Part 820, and cGMP requirements
- Working knowledge of Allen Bradley PLCs, Cognex Vision Systems, Fanuc Robots, and SQL databases preferred; strong expertise in at least one area will be prioritized
- Excellent communication and collaboration skills
- Ability to work independently or as part of a project team
- Experience analyzing manufacturing processes, implementing improvements, and validating changes
- Familiarity with Minitab or other statistical software preferred
Responsibilities may vary by project based on client needs and scope of work. Typical responsibilities may include:
- Lead and support troubleshooting and programming of automated systems, including PLCs, robots, vision inspection, communication systems, and database scripting
- Utilize analytical and statistical tools to resolve manufacturing issues
- Contribute to new equipment designs, focusing on validation requirements, maintainability, and reliability
- Lead or assist in the validation of new and modified equipment, processes, and test methods—including document generation, protocol execution, and reporting
- Support the creation and maintenance of process documentation
- Collaborate with cross-functional teams to meet project deliverables
- Interface with operators and clients to ensure alignment and support
If you meet the qualifications and are excited about supporting meaningful work in the life sciences space, we invite you to submit your application.
JVM Global is an equal opportunity employer. All applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran status, or disability status.
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