Overview of Andelyn Biosciences

Andelyn Biosciences is a biopharmaceutical Contract Development and Manufacturing Organization (CDMO) that specializes in advancing novel gene therapies from concept to commercialization.  Located in Columbus, OH, the company operates out of the Andelyn Corporate Center (ACC) for clinical and commercial cGMP manufacturing of viral vectors and plasmids and the Andelyn Development Center (ADC) for preclinical non-cGMP activities.

Our Values are founded in our origin story.

The name “Andelyn” is a hybrid of two gene therapy patients who participated in pivotal Phase I clinical trials at Nationwide Children’s Hospital. Andrew received the first U.S. investigational gene therapy for Duchenne muscular dystrophy in 2006. Evelyn received experimental gene therapy for spinal muscular atrophy in 2015. “Andelyn” combines their names to represent all the families who have courageously participated in the research that makes today’s gene therapies possible. 

 

Through this journey, we have been able to accelerate the development and manufacturing of innovative therapies to bring more treatments to more patients. We are Pioneering Solutions that Turn Hope into Reality™ through our ACCTSions.

 

ACCOUNTABLE in our actions.

CURIOUS to discover.

COMPASSIONATE in our thinking.         

TRUSTWORTHY in our communications.

SUPPORTIVE of one another.

 

Employees are expected to perform the following essential functions under the framework of our ACCTSions.

 

What you will do.

The Senior Business Systems Consultant – Digital Adoption plays a key role in driving the successful rollout, usage, and continuous improvement of digital systems across the Andelyn enterprise. This role is responsible for leading digital adoption initiatives, designing and delivering effective training programs, and authoring high-quality

technical documentation to support regulated and non-regulated system implementations. As a senior member of the Business Systems team, this individual will work cross-functionally with IT, Quality, Manufacturing, and other stakeholders to ensure that system users are enabled and equipped to realize the fullalue of digital tools in a GxP-compliant environment.

  • Lead digital adoption strategy for enterprise applications, with a focus on user enablement, change management, and onboarding.
  • Design and deliver tailored training programs for internal teams, including live sessions, eLearning modules, and on-demand resources.
  • Develop high-quality technical documentation including SOPs, Work Instructions, Quick Reference Guides, and eLearning content.
  • Serve as a subject matter expert on user experience and training best practices for digital systems, especially in GMP and regulated environments.
  • Partner with business process owners and application administrators to ensure training and documentation remain current and effective through system lifecycle changes.
  • Monitor system adoption metrics and feedback to continuously refine training and support approaches.
  • Contributes to the development of scalable knowledge repositories and searchable content libraries using modern digital tools.
  • Participate in project teams for the implementation or upgrade of enterprise platforms such as MES, LIMS, QMS, ERP, and eQMS.
  • Ensure all documentation and training materials align with compliance standards (FDA, GAMP 5, 21 CFR Part 11).

 

What you bring to the team.

  • 5+ years GMP/Biopharmaceutical/Biotech Industry or regulated industry preferred Bachelor’s Degree in Computer Science or equivalent educational and/or work experience. Version 1.0 Last Updated on 06.27.24
  • Manufacturing Systems, Quality/Lab Systems, Salesforce experience desired.
  • Strong experience working in a cross-functional team.
  • Demonstrated experience developing technical documentation and delivering training in a GxP environment.
  • Strong knowledge of system lifecycle processes (SDLC/CSA/CSV) and change management principles.
  • Excellent communication skills with ability to translate complex technical concepts into clear, user - friendly content.
  • Demonstrated desire to learn new technologies and ability to adapt to new operating models and changing business requirements effectively.
  • Must demonstrate a “can-do” attitude. 

 

What you can expect when working at Andelyn.

  • Pride in contributing to the development and manufacturing of lifesaving therapies.
  • The invaluable experience of being a part of building the foundation of a new organization.
  • The opportunity to collaborate with experts who have over 10 years in the gene therapy field.
  • Competitive compensation
  • Eligible on day one for medical, dental, and vision insurance plans with basic vision at 100% company-paid
  • 160 hours of Paid Time Off annually
  • 11 Company Paid Holidays plus 2 floating holidays annually.
  • Company Paid Life Insurance
  • 401(k) Match
  • Company Paid short and long-term disability.
  • 4 weeks of Paid Parental Leave for birth and adoption
  • Adoption Assistance
  • Tuition Reimbursement and Student Loan Repayment Assistance
  • Company Paid LinkedIn Learning access.
  • Employee Assistance Programs
  • Flexible work options (role specific)

 

Andelyn Biosciences embraces diversity and is an equal opportunity employer and does not discriminate based on race, religion, national origin, gender, gender identity, genetic information, sexual orientation, protected veteran status, disability, age, or another legally protected status. As an organization, we are committed to creating an environment where everyone ACCTS.

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