Back to jobs

Data Scientist II, Downstream

Columbus, Ohio

Job Title:  Data Scientist II, Process Development  

Department: Process Development - Downstream   

 

 

About the Role: 

The Data Scientist II will provide active leadership and execution of the data analysis and documentation improvements for downstream process development efforts. This individual will be responsible for leading data science initiatives within the team, driving data science projects from conception to implementation, set up procedures, manage junior scientists, foster innovation within the process development department to advance viral vector manufacturing process. This role provides an opportunity to play a significant impact in the success of client gene therapy programs. 

 

What You'll Do: 

  • Focus on extracting insights from production data to identify areas for improvement, predict potential issues, drive efficiency, automate data pipelines, and create insightful dashboards to support development and manufacturing.  
  • Lead data structuring, perform data analysis to build data trends and patterns, model development, and statistical analysis. 
  • Ensure innovative technologies and methodologies are employed to maintain the highest data quality standards while ensuring that activities occur in an efficient and GDP-compliant manner.  
  • Generate reports and contribute to responses to both internal and external stakeholders. 
  • Independently present results, work with cross-functional teams where necessary to prepare publications or reports in alignment with key stakeholders. 
  • Become a subject matter expert (SME) for our electronic lab notebook system, Benchling, our documentation and training system, Quality Management System (Veeva). 
  • Work closely with process development scientists to apply advanced data analytical techniques to understand and optimize the manufacturing process.  
  • Providing training to process development team members on data science and analytics including but not limited to the training curriculum. 
  • Review study protocols, and technical reports and approve documentation.  
  • Ensure reports are written to highest standards and manage documentation review and approvals to meet deadlines. 
  • Ensure data is maintained in an accurate and controlled manner. 
  • Support internal process transfer activities from Process Development to GMP. 
  • Provide training, leadership, and guidance to the team, share resources on best practices, and provide feedback.  
  • Effectively manage a team of Data Scientists to support process development needs.  
  • Provide technical guidance and mentorship to junior team members, promoting their personal growth and skill development. 
  • Collaborate closely with process development scientists, Manufacturing Sciences and Technology, cGMP, Compliance and Information technology teams to manage on the projects while adhering to relevant standards and company guidelines during product lifecycle. 

 

What You'll Bring: 

  • Bachelor’s degree in chemical engineering, Biomedical Engineering, Biology or related discipline (or equivalent experience) with a minimum of 10 years' experience. 
  • Experience in Data Science, Data Analytics, Data Engineering, or related discipline certification, or relevant coursework are a plus. 
  • Working knowledge of purification techniques such as chromatography, tangential flow filtration, clarification etc. is a plus. 
  • Understanding of manufacturing processes relevant to the industry (e.g., chemical engineering, pharmaceutical production) 
  • Knowledge of process control methodologies and quality standards. 
  • Proven ability to operate and troubleshoot purification equipment. 
  • Experience in planning, conducting, and reviewing experimental data with no oversight. 
  • Prior experience in training and development of other team members.  
  • Proven ability to manage team members effectively. 
  • Experience in analyzing datasets and utilizing the corresponding data to influence decision making. 
  • Skilled at organization and managing multiple projects simultaneously. 
  • Strong analytical and data interpretation skills to assess and drive quality improvement through the analysis of quality metrics and performance data. 
  • Experience working with at least two of the following: Benchling, Excel, JMP, SQL, or Power BI. 
  • Robust understanding of regulatory requirements as they pertain to process development and characterization. 
  • Excellent communication and collaboration skills to work effectively with cross-functional teams and to convey complex data insights to stakeholders. 
  • Problem-solving and critical thinking skills to identify root causes and propose solutions.  
  • Experience in leading, mentoring, and guiding junior team members. 
  • Strong understanding and experience in Electronic Quality Management Systems (EQMS), Laboratory Information Management Systems (LIMS), etc.and regulatory requirements relevant to the industry.  

 

Preferred Qualifications/ Skills: 

  • Master’s Degree or PhD in Chemical Engineering, Biomedical Engineering, Biology, or related discipline (or equivalent experience). 
  • Experience working with viral vectors (AAV, Lentivirus, etc.). 
  • Experience directly managing junior team members.    
  • Previous data or Software Engineering role in Biology, Chemistry, or other Life Science Industry. 
  • Proficiency in Python, R, and SQL, Predictive modeling, hybrid modeling 
  • Experience in machine learning algorithms (regression, decision trees, neural networks) 
  • Familiarity with big data tools and cloud platforms (AWS, Azure) 

 

Work Environment and Physical Requirements 

This position works in both a laboratory environment and typical office environment where the physical work demands will vary depending on the specific tasks and duties required of the job. The employee will be stationary (standing/sitting) for extended periods of time. Employees regularly wear personal protective equipment based on the task being performed. Must be able to work in a confined space, such as a clean room or laboratory environment. Ability to identify minute details within the field of vision, distinguish between distinct colors and accurately identify objects within a specific area.  

This job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee. Duties, responsibilities and activities may change or new ones may be assigned. 

Forge Biologics is an equal opportunity employer dedicated to building an inclusive and diverse workforce. Forge Biologics, provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.  

 

 

Life at Forge  

We are a team of diverse, driven and passionate people working together to trailblaze a new model for how we make medicines to treat patients with genetic diseases. Our team members use their creativity and talent to invent new solutions, meet new demands, and offer the most effective services in the industry. Forge’s core values lay the foundation for H.O.P.E. It provides us a common purpose that we all understand, work towards and live by.  

 

HARDWORKING - We work hard and smart, making a persistent and determined effort toward success. Working hard, with focus and desire is the key. 

OPEN - We strive to be approachable, actively listen and encourage others to contribute and speak up. We positively offer and receive constructive feedback. 

PURPOSE DRIVEN - We are passionate about working towards and delivering on our mission to manufacture gene therapies. 

ENGAGED - We are fully absorbed by and enthusiastic about our work and take positive action to further Forge’s vision, mission and goals. 

 

We’ve Got You Covered 

We take the health and happiness of our employees seriously and are consistently evaluating new ways to make our benefits truly UnFORGEttable. 

Health, Dental, and Vision insurance that starts on your first day at Forge, with 90% of premiums covered for team members as well as dependents 

Competitive paid time off plan 

Annual bonus for all full-time employees 

401(K) company match 

Fully-stocked kitchen with free food/drinks 

12 weeks of paid parental leave - additional discount programs include childcare support & dependent care 

Employee Assistance Program  

Wellness benefits (financial planning services, mental health counseling, employer paid disability) 

Onsite fitness facility  

Professional & Personal development resources  

 

 

Apply for this job

*

indicates a required field

Resume/CV*

Accepted file types: pdf, doc, docx, txt, rtf

Cover Letter

Accepted file types: pdf, doc, docx, txt, rtf


Select...
Select...
Select...

Voluntary Self-Identification

For government reporting purposes, we ask candidates to respond to the below self-identification survey. Completion of the form is entirely voluntary. Whatever your decision, it will not be considered in the hiring process or thereafter. Any information that you do provide will be recorded and maintained in a confidential file.

As set forth in Forge Biologics’s Equal Employment Opportunity policy, we do not discriminate on the basis of any protected group status under any applicable law.

Select...
Select...
Race & Ethnicity Definitions

If you believe you belong to any of the categories of protected veterans listed below, please indicate by making the appropriate selection. As a government contractor subject to the Vietnam Era Veterans Readjustment Assistance Act (VEVRAA), we request this information in order to measure the effectiveness of the outreach and positive recruitment efforts we undertake pursuant to VEVRAA. Classification of protected categories is as follows:

A "disabled veteran" is one of the following: a veteran of the U.S. military, ground, naval or air service who is entitled to compensation (or who but for the receipt of military retired pay would be entitled to compensation) under laws administered by the Secretary of Veterans Affairs; or a person who was discharged or released from active duty because of a service-connected disability.

A "recently separated veteran" means any veteran during the three-year period beginning on the date of such veteran's discharge or release from active duty in the U.S. military, ground, naval, or air service.

An "active duty wartime or campaign badge veteran" means a veteran who served on active duty in the U.S. military, ground, naval or air service during a war, or in a campaign or expedition for which a campaign badge has been authorized under the laws administered by the Department of Defense.

An "Armed forces service medal veteran" means a veteran who, while serving on active duty in the U.S. military, ground, naval or air service, participated in a United States military operation for which an Armed Forces service medal was awarded pursuant to Executive Order 12985.

Select...

Voluntary Self-Identification of Disability

Form CC-305
Page 1 of 1
OMB Control Number 1250-0005
Expires 04/30/2026

Why are you being asked to complete this form?

We are a federal contractor or subcontractor. The law requires us to provide equal employment opportunity to qualified people with disabilities. We have a goal of having at least 7% of our workers as people with disabilities. The law says we must measure our progress towards this goal. To do this, we must ask applicants and employees if they have a disability or have ever had one. People can become disabled, so we need to ask this question at least every five years.

Completing this form is voluntary, and we hope that you will choose to do so. Your answer is confidential. No one who makes hiring decisions will see it. Your decision to complete the form and your answer will not harm you in any way. If you want to learn more about the law or this form, visit the U.S. Department of Labor’s Office of Federal Contract Compliance Programs (OFCCP) website at www.dol.gov/ofccp.

How do you know if you have a disability?

A disability is a condition that substantially limits one or more of your “major life activities.” If you have or have ever had such a condition, you are a person with a disability. Disabilities include, but are not limited to:

  • Alcohol or other substance use disorder (not currently using drugs illegally)
  • Autoimmune disorder, for example, lupus, fibromyalgia, rheumatoid arthritis, HIV/AIDS
  • Blind or low vision
  • Cancer (past or present)
  • Cardiovascular or heart disease
  • Celiac disease
  • Cerebral palsy
  • Deaf or serious difficulty hearing
  • Diabetes
  • Disfigurement, for example, disfigurement caused by burns, wounds, accidents, or congenital disorders
  • Epilepsy or other seizure disorder
  • Gastrointestinal disorders, for example, Crohn's Disease, irritable bowel syndrome
  • Intellectual or developmental disability
  • Mental health conditions, for example, depression, bipolar disorder, anxiety disorder, schizophrenia, PTSD
  • Missing limbs or partially missing limbs
  • Mobility impairment, benefiting from the use of a wheelchair, scooter, walker, leg brace(s) and/or other supports
  • Nervous system condition, for example, migraine headaches, Parkinson’s disease, multiple sclerosis (MS)
  • Neurodivergence, for example, attention-deficit/hyperactivity disorder (ADHD), autism spectrum disorder, dyslexia, dyspraxia, other learning disabilities
  • Partial or complete paralysis (any cause)
  • Pulmonary or respiratory conditions, for example, tuberculosis, asthma, emphysema
  • Short stature (dwarfism)
  • Traumatic brain injury
Select...

PUBLIC BURDEN STATEMENT: According to the Paperwork Reduction Act of 1995 no persons are required to respond to a collection of information unless such collection displays a valid OMB control number. This survey should take about 5 minutes to complete.