Associate Scientist/Scientist/Sr. Scientist - Upstream Process Development
About Enlaza Therapeutics
Enlaza Therapeutics is a biotech company developing an innovative synthetic biology platform to create a disruptive new class of biologic therapeutics.
We are dedicated to the development of these novel therapies to help patients suffering from cancer and other serious diseases.
Role Description :
As a key member of the Upstream Process Development Team, the candidate will play a crucial role in designing and optimizing bioreactor processes to produce protein biologics from E.
coli . The role requires a balance of hands-on lab work and mentoring junior team members. The successful candidate will possess deep technical expertise in upstream process development and a collaborative spirit to work effectively across internal teams.
Responsibilities :
- Design, plan, and execute on key experiments to further Upstream Process Development of the proprietary Enlaza protein production platform, including assisting in the setup and breakdown of bioreactors.
- Enhance manufacturing technologies, capabilities, and processes including, optimizing media, physical conditions, feed profiles, and scale-up.
- Mentor and guide junior team members in experimental protocols, troubleshooting experimental issues, and equipment handling.
- Generate, manage, evaluate, and maintain critical data with high organizational standards, including the initial vetting of bioreactor run integrity.
- Improve ELN templates and develop tools for more efficient bioreactor data collection and presentation.
- Author comprehensive technical reports, tech transfer documents, and SOP’s
- Prepare and deliver scientific presentations as required.
- Collaborate closely with cross-functional scientists to meet project goals and produce required proteins.
- Ensure the maintenance of UPD group inventory, including cell banks, stock solutions, and materials; oversee the troubleshooting of operational processes and equipment issues.
Qualifications / Requirements :
- BS in Biochemical Engineering, Biological Sciences, or a related field with 5+ years relevant industry experience, or MS with 2+ years relevant industry experience.
- Extensive experience with manufacturing cell culture process development, primarily with microbial systems.
- Proven hands-on experience with small-scale bioreactor set-up and operations, along with flasks.
- Strong laboratory skills, including molecular biology techniques (e.g., western blots)
- Demonstrated ability to write detailed technical documents such as tech transfer documents, SOPs, and progress reports.
Preferred
- Direct experience with E. coli upstream process development for biologics.
- Proficiency in programming reactor control systems, e.g. DASware and Applikon Lucculus.
- Experience with Benchling, particularly with Benchling insights or API.
- Experience with advanced data analysis tools and software, such as Python, or JMP.
- Familiarity with cGMP and tech transfer to CDMOs
- Knowledge of regulatory requirements and quality control processes for biologics production.
- Experience in project management or leading projects in a biotech or pharmaceutical setting.
- Strong communication and interpersonal skills for effective cross-functional collaboration.
- Demonstrated problem-solving skills and innovative thinking.
Compensation :
In addition to a competitive compensation package with stock options, the company also offers a comprehensive benefits package for our employees and their families, which includes medical, dental, vision, and supplemental disability insurance.