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Scientist I - Analytical Development

Andelyn Biosciences
Dublin, OH
Start date
Aug 8, 2022

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Job Details

It’s an exciting time to join us!

The Andelyn Biosciences’ Analytical Development group is seeking a motivated individual to join our growing team as a Scientist I – Analytical Development.

The Scientist I will be responsible for execution of various molecular biology, chemistry, microbiology, and protein chemistry assays to support analytical development of manufactured products. All work is conducted under strict adherence to standard operating procedures and following good documentation practices. Secondary responsibilities include assist in peer review of analytical development testing documentation, SOP generation or revision, report writing, and other tasks needed to support the primary responsibilities.


Schedule: Full-time (Benefits Eligible)  

Location:  Dublin Campus 

                  5185 Blazer Pkwy #102

                  Dublin, OH 43017 


Under the guidance and direction of the Supervisor – Analytical Development essential functions of the Scientist I – Analytical Development include at a minimum:

  • Execute experiments as directed to satisfy development, qualification, validation, and routine testing as applicable
  • Displays basic technical knowledge of the instruments, assays, and scientific principles used in the laboratory
  • Respond to, and act 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
  • 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 CMF
  • 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 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
  • Other duties as assigned


Knowledge, Skills and Abilities required: 

  • Must possess 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
  • Frequently Talking on phone or in person
  • Frequently Typing on a computer keyboard


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.


EOE M/F/Disability/Vet


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.




Andelyn Biosciences is a biopharmaceutical CDMO Pioneering Solutions That Turn Hope into Reality™. With 20+ years of experience manufacturing viral vectors, Andelyn's scientific expertise for development and characterization has led to GMP material being produced for over 75+ worldwide clinical trials and 400+ cGMP clinical batches. Advanced quality systems, full regulatory support, and supply chain vertical integration help accelerate the development and manufacturing of innovative therapies to bring more treatments to more patients. The name "Andelyn" is a hybrid of two gene therapy pioneers 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, representing all the families who have courageously participated in the research that make today's gene therapies possible. Continuing Andelyn's patient-based mission, the company is opening two state-of-the-art commercial manufacturing and development sites. The Dublin-based Andelyn Development Center is set to open in May 2022 and will house Andelyn's preclinical and development services. The 185,000 square foot Andelyn Corporate Center located on The Ohio State University's Innovation District will open for production in mid-2022.  

Find Us
515 E. Main St
United States
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