Design Transfer Engineer​/Senior Design Transfer Engineer

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R&D - Design Transfer Full-Time Professional Alachua, FL, US

4 days ago Requisition

Salary Range: $ To $ Annually

Location: Alachua, FL

We are currently recruiting for either a Design Transfer Engineer 2 or Sr. Design Transfer Engineer
, depending on the candidate's experience and qualifications.

Below are the salary ranges and potential annual bonus opportunities for each level:

Potential Annual Bonus:
Up to $8,000

Potential Annual Bonus:
Up to $10,000

The position level and compensation will be determined based on the selected candidate's experience and qualifications .

Evergen is a global industry-leading contract development and manufacturing organization (CDMO) in regenerative medicine. As the only regenerative medicine company that offers a differentiated portfolio of allograft and xenograft biomaterials at scale, Evergen is headquartered in Alachua, FL, and has manufacturing facilities in West Lafayette, IN;
Eden Prairie and Glencoe, MN;
Neunkirchen, Germany; and Marton, New Zealand.

We are proud to be Great Place to Work® Certified in 2026
, reflecting our commitment to creating an exceptional employee experience and workplace culture. Evergen currently has full-time career opportunities available across multiple locations.

• Paid Time Off (PTO)
• 401(k) with company match
• Holiday pay
• Medical, dental, and vision insurance
• Short-term and long-term disability coverage
• Serves as a lead core team member of a cross functional project team whose responsibilities include conducting studies directed toward the development of processes
• Performs standard scientific assignments to evaluate results for validity and conformance to acceptable scientific methods. Independently determines requirements and acceptance criterion associated with testing performed.
• Applies deep knowledge of six sigma methodologies (process capability, SPC, etc.) to assess product design and translate them into process specifications
• Participates and consults with the internal and external scientific community to maintain a state-of-the-art knowledge for application to achieving successful experimental outcomes
• Deploys deep knowledge of manufacturing to suggest and implement creative solutions in process development and test method creation innovating manual hand driven processes to semi-automated equipment driven processes.
• Coordinates or performs validations and documents risk management activities to support regulatory submissions or product launches
• Leverages expertise across projects and specialties to effectively accomplish assignments and identify and mitigate risks within a project.
• Leverages clinical and technical expertise to evaluate design and process risks and implement effective mitigation measures
• Exhibits functional autonomy through creating project direction assigning design transfer deliverables required to support both new product development projects and design change projects
• Reviews and edits internal documentation for team members and assists in the preparation and presentation of materials for internal or external technical reviews
• May serve as a team lead and have direct reports
• Supports Quality process improvement initiatives
• Other duties as assigned

• Bachelor of Science Degree in relevant area

• 6+ years of relevant medical device, pharmaceutical, or other regulated industry experience

• N/A

• Excellent verbal and written communication
• Project Management
• Microsoft Office Suite
• Design Transfer
• Laboratory Testing
• Design software

• N/A

• Move or lift objects up to 25 pounds
• Frequent (>75%) stationary…