Senior Design Transfer Engineer

Evergen (Formerly RTI Surgical)

Lead Design Transfer Engineer at Evergen, a CDMO in regenerative medicine. Collaborating with cross-functional teams for process development and regulatory submissions.

Posted 6/19/2026full-timeEden Prairie • Minnesota • 🇺🇸 United StatesSenior💰 $110,000 - $130,000 per yearWebsite

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

six sigma methodologiesmicrobiological techniquesaseptic processingprocess developmenttest method creationrisk managementvalidationscientific methodsdocumentation practicesquality process improvement

Soft Skills

attention to detailindependent workeffective communicationcross-functional collaborationproblem-solvinginvestigative mindsetleadershipteam coordinationcreativityproject management

Certifications & Qualifications

Bachelor’s degree

Industry Keywords

medical devicepharmaceuticalregulated industryprocess specificationsregulatory submissionsproduct launchesscientific communityrisk mitigationcross functional project teamscientific assignments

About the role

Key responsibilities & impact

Serves as a lead core team member of a cross functional project team
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 to assess product design and translate them into process specifications
Participates and consults with the internal and external scientific community
Deploys deep knowledge of manufacturing to suggest and implement creative solutions in process development and test method creation
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
May serve as a team lead and have direct reports
Supports Quality process improvement initiatives

Requirements

What you’ll need

Bachelor’s degree in relevant area
6+ years of relevant medical device, pharmaceutical, or other regulated industry experience
Strong attention to detail and documentation practices
Ability to work independently in a small-company environment
Effective communication and cross-functional collaboration
Problem-solving and investigative mindset
Strong knowledge of microbiological techniques and aseptic processing

Benefits

Comp & perks

Annual CIP bonus opportunity of up to $13,000.00