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R&D Engineer 2

Evergen
West Lafayette, IN Full Time
POSTED ON 11/12/2025 CLOSED ON 12/30/2025

What are the responsibilities and job description for the R&D Engineer 2 position at Evergen?

Location: West Lafayette, IN 

 

RTI Surgical is now Evergen!

 

This rebranding reflects our strategic evolution as a leading CDMO in regenerative medicine and comes at the end of a significant year for the business, including the successful acquisitions of Cook Biotech in IN. and Collagen Solutions, MN. Our new brand identity emphasizes our unique positioning as the only CDMO offering a comprehensive portfolio of allograft and xenograft biomaterials at scale.

 

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, DE., Glasgow, UK., and Marton, NZ.  

 

Read more about this change and Evergen’s commitment to advancing regenerative medicine here: https://lnkd.in/eMSfVJkM ;     

 

RESPONSIBILITIES

  • Leads project workstreams in the design and development of new devices and improvements to existing designs leveraging previous experience with minimal support to derive unique solutions and approaches to drive project success
  • Applies sound engineering problem-solving techniques to resolve challenges during the product development process and analyzes data to draw conclusions using statistically sound and scientifically-based methodology
  • Leverages experience and technical knowledge to proactively develop strategies and plans of execution to derive unique solutions and approaches to contribute to project success
  • Writes protocols, reports, Standard Operating Procedures (SOPs), and other technical documents in accordance with Good Documentation Practices with a high attention to detail. Applies principles of ISO 13485 and ISO 14971
  • Designs, develops, and validates test methods to meet design requirements. 
  • Effectively leads discussions and builds consensus with quality, regulatory, engineering, and production teams throughout the product development process to meet project objectives
  • Leads discussions with internal or external customers to obtain design requirements and feedback on prototype designs with a high level of customer service
  • Maintains project timelines by providing appropriate inputs, target times, and resource needs 
  • Applies clinical knowledge in relevant surgical procedures and disease states within a clinical segment to develop innovative solutions to satisfy customer needs
  • Evaluates product design for manufacturability and suggests design process adjustments and quality improvements
  • Participates in the selection, development, and testing of tools, fixtures, machinery, and equipment used in manufacturing
  • Other duties as assigned

REQUIREMENTS

Education

  • Bachelor’s of Science Degree in Biomedical Engineering or another relevant engineering discipline.

Experience

  • 4 to 6 years of engineering experience designing or modifying medical devices or implants.

Certification

  • N/A

Skills 

  • Excellent verbal and written communication skills
  • Effective negotiation skills
  • Competency in Enterprise Resource Planning (ERP) software
  • Computer program expertise and knowledge of Microsoft Suite, especially Excel
  • Continuous Improvement methodologies 

Travel 

  • 10% or less

SAFETY

 

Physical Requirement

  • 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 (typing, opening, writing, clicking, paper sorting, etc.)

 

Working Environment

  • Onsite: Office environment with assigned workstation
  • Remote positions only: Home office environment with minimum distractions. 

More about Evergen:

 

Evergen provides customers across a diverse set of market segments with leading-edge expertise, scale, and flexibility across end-to-end services including design, development, regulatory support, verification and validation, manufacturing, and supply chain management. 


 Evergen is rooted in a steadfast commitment to quality, integrity, and patient safety with a focus on five key values:

  • Accountable: We own our actions and decisions.
  • Agile: We embrace change to stay ahead of the curve and evolve to drive innovation and growth. 
  • Growth Mindset: We embrace challenges as opportunities for continuous learning.
  • Customer-Centric: We prioritize customers at every touch point. 
  • Inclusive: We thrive on the richness of our diversity and ensure every voice is heard, respected, and celebrated. 

At Evergen, we are committed to fostering an inclusive workplace where we embrace the richness of our diversity and ensure that every voice is heard, respected, and celebrated. We believe that by embracing diversity and promoting inclusivity, we not only uphold our values but also strengthen our position as the CDMO of Choice in regenerative medicine solutions. We recognize that cultivating a growth mindset is essential to our success, and we are dedicated to continuous learning and improvement in our diversity, equity, and inclusion efforts. Through accountability and action, we strive to create an environment where individuals can thrive, innovate, and contribute their unique perspectives to drive our collective success.

 

Montagu Private Equity (“Montagu”), a leading European private equity firm, acquired RTI in 2020 and has supported the transformation of the company to its next level of potential.


#LI-Onsite

 



Salary : $70,000 - $90,000

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