DESCRIPTION

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 Plasmid Department at Andelyn Biosciences is seeking a Scientist I - Plasmid Production Core. The primary responsibility for the Scientist I Plasmid Production Core role is to provide hands on assistance for all day-to-day plasmid production operations, including execution of production processes, documentation, as well as preparation and inventory maintenance of solutions prepared in-house for use in plasmid production processes. This role will support production efforts to deliver all products in a timely, compliant, and fiscally responsible fashion by following appropriate practices, batch records, and Operating Procedures (OPs) for manufacturing biological products.

 

Schedule: Full-time (Benefits Eligible) 

 

Location: 

Central Campus 

700 Children's Drive

Columbus, OH 43205 

 

Under the guidance and direction of the Plasmid Manager, the essential functions of the Scientist I – Plasmid Production Core:

  • Responsible for assisting in the support of the production of plasmids used for basic research and toxicology studies.
  • Additional responsibilities include coordinating and preparation of critical solutions used in the production of plasmids for research studies.
  • Maintain compliance with applicable regulatory requirements for cellular and gene therapy products.
  • Attention to detail in all job functions.
  • Performs in accordance with established policies, procedures, and techniques and requires training common experience or working knowledge related to the tasks performed.
  • Identifies problems and performs tasks as assigned.
  • Work under general supervision of senior staff and leadership.
  • Works in diverse and collaborative team environment utilizing clear communication to deliver high productivity and contributes to the success of team and goals.
  • Documentation of all activities performed according to Operating Procedures (OPs).
  • Nominal fiscal responsibility.
  • Exercise discretion, judgment, and personal responsibility.
  • Demonstrate high level of integrity.
  • Maintain positive attitude.
  • Other duties as assigned.


Knowledge, Skills and Abilities required:


 ·   Relevant four-year degree experience in microbiology, molecular biology, biochemistry or related field preferred.

·    No minimum experience.

·    Effective communication and interpersonal skills required

·    Experience in highly regulated field preferred

·    Skills in operating a personal computer, and word processor

·    Must be familiar with various software packages (e.g., Word, Excel, PowerPoint)

 

Preferred Skills:

·    Understanding of large-scale plasmid production.


·    Experience using bioreactors.

·    GMP-experienced individual.

·    Experience in highly regulated field.

 

Minimum Physical Requirements

·       Sitting Constantly                             Frequently

·       Talking on the phone/in person         Frequently

·       Typing on a computer keyboard        Frequently

·       Standing/walking                               Occasionally    

                                                                       

 

EOE M/F/Disability/Vet

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