It’s an exciting time to join us!

The Andelyn Biosciences’ Viral Vector Core group is seeking a motivated individual to join our growing team as a Scientist I.

Scientist I is responsible for supporting the gene therapy team by overseeing both the mammalian cell culture, prepared solution preparation, an AAV vector production, and purification. This includes ensuring the cell culture activities needed to meet the production schedule are planned, assisting in the preparation and inventory maintenance of solutions prepared in-house, and organizing the daily workloads for the production and purification of AAV vectors. The Scientist I will be responsible for adhering to VVC policies, protocols, and SOPs and following appropriate documentation procedures for preclinical AAV manufacturing.   The Scientist I will work with other VVC staff to expand their knowledge base and skill set.  Additionally, as the Scientist, I will learn to troubleshoot issues as well as trend errors and work with management to identify areas for process improvement. 

 

Schedule: Full-time (Benefits Eligible)  

Location:  Andelyn Development Center

                  5185 Blazer Pkwy

                  Dublin, OH 43017 

 

 

Under the guidance and direction of the Associate Director of Viral Vector Core, essential functions of the Scientist I - VVC:

  • Respond to, and take action from, alarm notifications from the applicable monitoring system(s) for laboratory temperature-controlled storage units that occur at any point during the assigned period of responsibility
  • Ensure the cell culture activities needed to meet the production schedule are planned, assisting in the preparation and inventory maintenance of materials and solutions prepared in-house and organizing the daily workloads for the production and purification of AAV vectors
  • Adhere to VVC policies, protocols, and SOPs and follow appropriate documentation procedures for preclinical AAV manufacturing  
  • Work with other VVC staff to expand their knowledge base and skillset 
  • Learn to troubleshoot issues as well as trend errors and work with management to identify areas for process improvement 
  • Perform all processes for research-grade and toxicology grade production at all scales following SOPs and protocols
  • Performs in accordance with established policies, procedures, and techniques and requires training common experience or working knowledge related to the tasks performed
  • Assist with Material Inventory in the lab and through SAP (ie. input ITRs)
  • Exercise discretion, judgment, and personal responsibility
  • Demonstrate a high level of integrity
  • Maintain a positive attitude
  • Operate within the Quality Management System applicable to the manufacture of phase appropriate material in the VVC
  • Maintain compliance with applicable regulatory requirements for cellular and gene therapy products
  • Attention to detail in all job functions with a strong focus on safety
  • Identifies problems and performs tasks as assigned
  • Work under the general supervision of senior staff and leadership
  • Works in a 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 SOPs
  • Make decisions based on established procedures
  • Nominal fiscal responsibility
  • Limited involvement in customer relations
  • Other duties as assigned

 

Knowledge, Skills and Abilities required

  • Must possess a relevant four-year degree, background in the life sciences, biotechnology, or gene therapy industries preferred
  • No minimum experience
  • Experience in highly regulated field preferred
  • Excellent communication, organization, and project management skills with the ability to manage multiple projects efficiently and adjust as priorities change
  • Must be literate in Microsoft Office (PowerPoint, Excel, Word)
  • Ability to work independently as well as collaboratively in a diverse and inclusive work environment.
  • Must possess a client-focused mindset in daily tasks
  • Must possess prior experience handling confidential information and the ability to maintain confidentiality

 

 Minimum Physical Requirements

  • Frequently Sitting
  • Frequently Walking/Standing/Stooping
  • Occasionally Independently lifting up to 50 pounds
  • Occasionally Talking on the phone or in-person
  • Typing on a computer keyboard
  • Frequently wear PPE regularly

                                                                                   

The above list of duties is intended to describe the general nature and level of work performed by individuals assigned to this classification. It is not to be construed as an exhaustive list of duties performed by the individual so classified, nor is it intended to limit or modify the right of any supervisor to assign, direct, and control the work of employees under his/her supervision.

 

Andelyn Biosciences is committed to a diverse and inclusive workplace. Andelyn is an equal opportunity employer and does not discriminate based on race, national origin, gender, gender identity, sexual orientation, protected veteran status, disability, age, or another legally protected status.

 

Andelyn Biosciences is currently operating under Executive Order 14042 that requires that employees of federal contractors and its affiliates be vaccinated against COVID-19, with some limited exemptions under the law.  As Andelyn is both an affiliate and will be a federal contractor, proof of vaccination status will be required prior to first date of employment.  Religious and medical exemptions may be considered depending upon the specific job duties and in accordance with applicable federal guidelines.

 

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