Andelyn Biosciences is an industry leading cGMP production facility dedicated to advancing the field of gene therapy. Our mission is to use our knowledge, resources, technology, and experience in the field of translational and regulatory science, to develop new, safe, and effective long-term treatments for diseases. There is no disease too rare and no challenge too difficult as we strive to make a difference with every product and to leave hope on the minds of every patient and their families. Andelyn is primarily a full-service manufacturer of Adeno Associated Virus (AAV). We work with over 100 clients each year to manufacture AAV at development, toxicology, clinical and commercial quality.
The Program Coordinator will support the Program Managers to exceed client satisfaction through driving multifunctional team coordination and successfully delivering complex customer projects on time, within budget, and on quality.
Principal Duties and Responsibilities
- Building timelines based on client needs for gene therapy programs, typically involving multiple platform technologies as well as customized solutions
- Acting as Andelyn’s customer interface and customer advocate during project delivery
- Ensuring an excellent customer experience
- Supporting project timelines and deliverables
- Streamlines Client program requests into our processes
- Organizing program documentation
- Ensuring project execution is performed in compliance with existing procedures
- Utilizing project management tools and processes
Knowledge, skills and abilities required
- Strong process development and analytical development understanding
- Familiarity with technical/scientific agreements and contracts.
- Bachelor’s degree
- Excellent organizational skills
- Outstanding communication skills
- Capable of being effective in connecting cross-functionally with people, bringing sites and functions together
- Understanding micro/macro-level operations across various functions, including Manufacturing, Quality, and Supply Chain
- Emotional Intelligence
- Experience in the highly regulated scientific industry and/or CDMO environment in rapidly evolving industry
Minimum Physical Requirements
- Sitting for extended periods Constantly (67-100%)
- Talking on the phone/in person Constantly (67-100%)
- Typing on a computer keyboard Constantly (67-100%)
- Standing/walking Occasionally (0-33%)
EOE M/F/Disability/Vet