Manufacturing Engineer IV – Process Engineering (Onsite)
Contract Duration: 6 months (with likely potential to extend)
Pay Rate: $68/hour
Work Authorization: Candidates must be authorized to work in the U.S. now and in the future. Visa sponsorship is not available for this role.
About the Role
We are seeking an experienced Manufacturing / Process Engineer IV to lead clinical build lines and drive critical process development activities that support product commercialization. In this highly visible role, you’ll own key deliverables such as process characterization, validation documentation, and production readiness, working closely with cross-functional partners to bring innovative technologies to market.
This is an onsite, hands-on engineering role ideal for someone who thrives in complex manufacturing environments and enjoys leading technical initiatives from development through production.
What You’ll Do
- Lead clinical build line activities, supporting process development and commercialization efforts
- Own and deliver process validation documentation and process characterization studies
- Partner cross-functionally with R&D, Process Development, Quality, Production, Regulatory, Equipment Engineering, Supply Chain, and Marketing to ensure project success
- Drive innovative process improvements using data-driven and Six Sigma methodologies
- Design, coordinate, and execute complex engineering tests and experiments
- Analyze complex data sets, draw clear conclusions, and communicate findings to technical stakeholders
- Prepare detailed technical reports, specifications, and process documentation
- Evaluate new technologies, equipment, and process changes for feasibility and robustness
- Manage Capital Equipment Request Authorizations (CERAs) from justification through implementation
- Lead and influence cross-functional project teams toward production and quality goals
- Train, mentor, and provide technical direction to operators, technicians, and engineers
Quality & Compliance
- Embed quality into all engineering activities
- Ensure compliance with all applicable quality system and regulatory requirements
What We’re Looking For
- 5+ years of relevant engineering experience in manufacturing or process development
- Bachelor’s degree in Engineering (Mechanical, Chemical, Biomedical, or related field)
- Strong background in process development, validation, and production support
- Proven ability to lead complex technical projects in a cross-functional environment
Nice to Have / Highly Valued Experience
- Knowledge of electropolishing processes
- Hands-on experience with Keyence and Sensofar measurement technologies
Why This Role
- High-impact engineering role supporting clinical builds and commercialization
- Opportunity to lead technically and influence manufacturing strategy
- Collaborative environment with strong cross-functional exposure
- Competitive hourly rate and meaningful, hands-on work
