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Senior Design Transfer Engineer
Evergen (Formerly RTI Surgical). Serve as a lead core team member of a cross-functional project team conducting studies toward process development .
Posted 10/27/2026full-timeAlachua • Florida • United StatesSenior💰 $100,000 - $120,000 per yearWebsite
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in process development and validation within regulated industries, applying Six Sigma methodologies and project management skills to drive quality improvements and successful product launches.
Highest-signal resume keywords
Six Sigma MethodologiesProject ManagementDesign TransferLaboratory TestingRegulatory Submissions
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Process DevelopmentScientific EvaluationRisk ManagementProcess CapabilitySPCManufacturing ExpertiseValidationTechnical DocumentationDesign SoftwareQuality Process Improvement
Soft Skills
Excellent Verbal CommunicationExcellent Written Communication
Tools & Technologies
Microsoft Office SuiteSemi-Automated Equipment
Industry Keywords
Medical DevicePharmaceuticalRegulated IndustryCross-Functional TeamProduct Design
About the role
Key responsibilities & impact- Serve as a lead core team member of a cross-functional project team conducting studies toward process development
- Perform scientific assignments and evaluate results for validity and conformance to acceptable scientific methods
- Determine requirements and acceptance criteria for testing
- Apply Six Sigma methodologies, including process capability and SPC, to assess product design and translate findings into process specifications
- Consult with internal and external scientific communities
- Apply manufacturing expertise to develop processes and test methods, including semi-automated equipment-driven processes
- Coordinate or perform validations and document risk management activities supporting regulatory submissions or product launches
- Evaluate design and process risks and implement mitigation measures
- Create project direction and assign design transfer deliverables for new product development and design change projects
- Review and edit internal documentation and assist with technical review presentations
- May serve as a team lead and have direct reports
- Support Quality process improvement initiatives
- Perform other duties as assigned
Requirements
What you’ll need- Bachelor of Science Degree in relevant area
- 6+ years of relevant medical device, pharmaceutical, or other regulated industry experience
- Excellent verbal and written communication
- Project Management
- Microsoft Office Suite
- Design Transfer
- Laboratory Testing
- Design software
- Ability to move or lift objects up to 25 pounds
- Frequent (>75%) stationary position (standing or sitting) while utilizing digital displays
- Frequent (>75%) fine manipulation using hands and fingers
- Onsite office environment with assigned workstation
Benefits
Comp & perks- Annual bonus opportunity up to $10,000
- Paid Time Off (PTO)
- 401(k) with company match
- Holiday pay
- Medical, dental, and vision insurance
- Short-term and long-term disability coverage
- Paid parental leave