Research Associate – Upstream Process Development

About Enlaza Therapeutics

Enlaza Therapeutics is a biotech company developing an innovative synthetic biology platform to create a unique class of biological medicines. We are dedicated to the development of treatments for serious disease and delivering these to patients.

Role Description

As part of the Upstream Process Development Team, the Research Associate is expected to assist in conducting experiments to define robust bioreactor processes to produce protein biologics from E. coli and help develop scalable processes suitable for cGMP production.

This role will encompass unit operations which are typically seen in an upstream function and require cross-collaboration with internal platform development along and downstream team members. A successful candidate will have technical knowledge and experience in upstream process development and a drive to learn.

Responsibilities
  • Help plan and execute on key experiments to further Upstream Process Development of the proprietary Enlaza protein production platform.
  • Maintain UPD group inventory including cell banks, stock solutions, and materials; and troubleshoot processes and equipment.

  • Contribute to the enhancement of manufacturing technologies, capabilities, and processes through (e.g., optimize media development, bioreactor fed-batch, and scale-up).
  • Generate, manage, evaluate, and maintain critical data in a highly organized and timely manner; Maintain and improve ELN templates.
  • Assist in authoring technical reports, tech transfer documents, and SOP’s.
  • Prepare scientific presentations as needed. Write/revise SOPs as needed.
  • Work closely with scientists across functions to produce the proteins required to meet project goals.
Requirements
  • BS in Biochemical engineering or Biological Sciences with 1+ years industry experience, or MS.
  • Exposure to industrial cell culture process development, primarily with microbial systems.
  • Hands on experience with small-scale bioreactor set-up and operations, along with flasks.
  • Proficient laboratory skills, including quantitative sample transfer, consistent and reproducible media preparation and familiarity with molecular biology techniques (e.g. western blots).
  • Experience with writing technical documents such as tech transfer documents, SOPs, and progress reports.
  • Proficient with MS-Excel.
Preferred Additional Skills
  • Direct experience with E. coli upstream process development for biologics.
  • Experience with programming reactor control systems.
  • Experience with cGMP and tech transfer to CDMOs.
  • Experience with Benchling and JMP.
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.

Job Type

Full-time

Annual Salary Range

$75,000.00 – $95,000.00

Supplemental Pay Types

Bonus pay

Benefits
  • 401(k)
  • Dental insurance
  • Employee assistance program
  • Flexible schedule
  • Flexible spending account
  • Health insurance
  • Flexible spending account
  • Flexible vacation
  • Paid holidays
  • Life insurance
  • Paid time off
  • Parental leave
  • Retirement plan
  • Vision insurance

Application Form

  • Accepted file types: doc, docx, pdf, txt, rtf, odt, Max. file size: 50 MB.