Scientist II/III - Upstream Process Development

Genezen Inc.; Indianapolis (IN); On-site; USD 80,000 - 100,000; Full time

Job summary

A leading company in gene therapy is seeking a Scientist II/III to direct process development for viral vector production. The role involves establishing scalable processes, optimizing performance, and ensuring compliance with GMP standards. Ideal candidates will have a strong background in biological engineering and relevant industry experience. Join a collaborative team dedicated to innovation and quality in healthcare.

Benefits

Paid vacation days

401(k) plan with company match

Choice of healthcare plans

FSA and HSA programs

Employer-paid life insurance

Qualifications

• 5-8 years of relevant industry experience.
• Solid foundation in biochemical engineering, virology, and cell biology.

Responsibilities

• Develop scalable platform for viral vector production processes.
• Monitor process performance and implement improvements.
• Design and execute experiments independently.

Skills

Attention to Detail

Problem Solving

Collaboration

Education

BS, MS, or PhD in Biological Engineering

Tools

Bioreactor

SOP/SSP

Job description

Scientist II/III - Upstream Process Development

Indianapolis, IN

The field of gene therapy is growing rapidly and Genezen is here to meet the exacting needs of our clients. We provide process development, produce GMP viral vectors, and provide cell transduction for gene and cell therapy clinical trials and are proud to be a part of the process that leads to new cures.

WORKING AT GENEZEN

Manypeople have worked in environments where you feel like just another nameless part of an enormous machine. Genezen is different. We want our employees to be innovative, collaborative problem solvers who are dedicated to meeting the challenges of working at a fast-growing company. We are dedicated to empowering our employees to be their best and making Genezen a rewarding place to work. Every employee contributes to the success of the company and you can be part of that team.

JOB SUMMARY

Direct the development and establishment of processes in Process Development. This individual is accountable for developing a scalable platform for viral vector production processes that minimizes the risk during Process Development to GMP scale-up. The individual will provide technical expertise and leadership in science & technology and requires close collaboration with internal stakeholders.

ESSENTIAL JOB FUNCTIONS

• Be accountable for establishing the platform from small scale through intermediate scale (50L) lentiviral and retroviral vector processes.
• Responsible for monitoring and reporting on process performance, identifying opportunities, and implementing changes to improve process, product safety, and product quality.
• Develop and support process optimization efforts to increase process robustness, reduce costs, and improve viral yield and purity.
• Design and execute experiments independently: accurately record, analyze, and communicate data to senior management and team members.
• Maintain open communication via one-on-one and team meetings.
• Stay current with relevant technologies and need to be adept at identifying new approaches.
• Perform and lead single-use system design manifold, selection, implementation, configurations in between Upstream bioreactor and downstream unit operations and control strategies.
• Develop proper SOP/ SSP for Upstream processes.
• Responsible for the process transfer from or to clients and to in-house manufacturing plant.
• Maintain external technical relationships and collaborate with equipment and material suppliers.
• Serve as process SME for regulatory and client audits.
• Ensure safe working environment and compliance with OSHA, EHS, Quality, and cGMP procedures and policies within the assigned functional area.

SPECIAL JOB REQUIREMENTS

• Adaptability required as work schedule may change based on business needs
• Criminal background check required
• Other duties as assigned

KNOWLEDGE, SKILLS AND EXPERIENCE

EDUCATION / CERTIFICATIONS / LICENSES

BS, MS, or PhD in biological engineering

ON-THE-JOB EXPERIENCE

5-8 years of relevant industry experience

Solid foundation in the fundamentals of biochemical engineering, virology and cell biology

Entrepreneurial experience dealing with customers in product development

Pharmaceutical industry experience in technical support of cGMP manufacturing and/or process development, including experience with Contract Development and Manufacturing Organizations

Experience with cell culture technologies, molecular biology, upstream processing, and aseptic processing

SKILLS / ABILITIES

Working knowledge of Upstream process (Cell culture, Aseptic,Technique, Transient transfection, PCL, single - use Bioreactor).

Ability to interface successfully with multi-disciplined teams

Extremely detail-oriented with strong technical skills & mechanically inclined/knowledge of hand tools

PHYSICAL DEMANDS

While performing the duties of this job, the employee is required to meet the following physical demands:

• Frequently required to work in a BSL 2 environment with personal protective equipment/aseptic gowning
• Regularly required to work around large machinery and typical utilities seen in pharmaceutical facilities
• Occasionally exposed to moving mechanical parts; high, precarious places; toxic or caustic chemicals; hazardous waste; and risk of electrical shock
• Occasionally exposed to extremely loud noise levels
• Spending time on the floor during activity execution (maintenance, construction, commissioning and qualification) is required

Movement

• Frequently required to stand; sit; use hands to finger, handle, or feel; reach with hands and arms
• Occasionally required to walk; climb or balance; and stoop, kneel, crouch, or crawl

Lifting

• Frequently lift and/or move up to 10 pound
• Occasionally lift and/or move up to 25 pounds

Vision

• Frequently utilize close vision and the ability to adjust focus

Communication

• Frequently required to communicate by talking, hearing, using telephone and e-mail

GENEZEN'S CURES VALUE-BASED COMPETENCIES

Committed to Science
We are committed toscientific excellence, staying current with industry developments, making data-driven decisions, and pursuing innovation to advance healthcare.

Urgency in action for the patients
We operate with urgency and a commitment to delivering timely treatments to patients by accelerating our partners' programs.

Resilience & Grit in operations
We are committed to overcoming challenges, learning from failures, and persistently striving for success.

Execute with Excellence & Integrity
We are dedicated to delivering quality results and upholding ethical principals.

Solutions driven for our partners
We are committed to being a proactive, collaborative, creative and open-minded partner.

GENEZEN'S BENEFITS

• Paid vacation days, amount based on tenure
• 401(k) plan with company match up to 6% of salary, vested immediately
• Choice of several healthcare plans
• FSA and HSA programs
• Employer-paid basic term life/personal accident insurance
• Voluntary disability, universal life/personal accident insurance

ADDITIONAL DETAILS

• Nothing in the job description for this role restricts management’s right to assign or reassign duties and responsibilities to this job at any time.
• This position requires a criminal background check.
• Genezen is an Equal Opportunity Employer.
• Genezen participates in EVerify.
• Genezen is interested in every qualified candidate who is eligible to work in the United States; however, we are not able to sponsor visas.

Genezen has operates two locations: one in Fishers, Indiana and the second in Lexington, Massachusetts.

Fishers is a suburb of Indianapolis. Fishers was named the #1 place to live in the US by Money Magazine in 2017 for its livability, safety and entrepreneurship. Fishers is one of the fastest growing communities in Indiana and is dedicated to supporting a high quality of life for all its residents. Nearby Indianapolis is home to professional and college sports teams, the Indy 500, a growing art community and the world’s largest children’s museum--to name just a few reasons why this area is a great place to live.

Lexington, Massachusetts, located just northwest of Boston, is renowned as a historic suburb with a rich cultural heritage. It boasts picturesque New England charm, tree-lined streets, and a vibrant community. Known for its pivotal role in the American Revolution, Lexington offers visitors and residents alike a blend of historical landmarks, modern amenities, and a strong sense of community pride.

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