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 Process Development laboratory at Andelyn Biosciences is seeking a highly motivated, organized individual for a Laboratory Technician/ Specialist position.  The ideal candidate must be able to work under pressure and coordinate numerous work streams within the lab to deliver timely, high-quality results. This position will be responsible for coordinating all administrative functions in the Process Development laboratory.

  • Work with the senior management in the PD department to ensure the laboratory is fit for use and in compliance with GxP practices.
  • Work with the senior management in the PD department to maintain laboratory material inventory on a regular basis.
  • Works with Business Development, Program Management and leadership to coordinate project scheduling and timelines within the PD department.
  • Work with the PD department and supply chain to ensure the ordering of supplies is up to date and in anticipation of upcoming PD projects.
  • Coordinates with Business Development and Program Management team for client-related SAP and LabWare needs.
  • Ensure work follows GxP practices and documentation where applicable including lab notebooks, research batch records, and SOPs.
  • Participates in a team environment; including fostering a culture of collaboration.
  • Partners directly with Quality, Engineering, and other departments to resolve equipment and laboratory maintenance related issues.
  • Coordinate development activities with other departments in the organization to resolve issues related to product manufacturing, testing, and performance.
  • Participate in technical transfer efforts to research and GMP production laboratories; initiating change controls, training, etc.
  • Assist in vendor selection and ordering of materials used in development work; active participation all areas of the material control system and SAP software.
  • Work with Laboratory Services to communicate with outsourced testing laboratories to ensure timely and quality results are generated consistently. Ensure appropriate documentation and results traceability.
  • Trains and documents orientations for new lab users on laboratory organization, workflows, Quality System compliance, and Safety requirements.

 

What you bring to the team.

  • A bachelor’s degree in a science related field or equivalent experience.
  • Experience with pharmaceutical laboratory and/or project management preferred.
  • Laboratory management using a SAP system, and experience with equipment validation is a plus.
  • Direct experience with gene therapy viral vector PD and/or manufacturing is a plus

 

What you can expect when working at Andelyn.

  • The pride of contributing to the development and manufacturing of life-saving therapies
  • The invaluable experience of being a part of building the foundation of a new organization.
  • The opportunity to work alongside experts that have over 10 years in the gene therapy field.
  • Competitive compensation
  • Eligible 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 Paid Holidays plus 2 floating holidays annually.
  • Company-paid 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.