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Associate Engineer/Engineer 1, Material Generation Lead

Boston, MA
Intergalactic Therapeutics is a bio-innovation company developing, delivering, and democratizing novel non-viral gene therapies for patients. Intergalactic’s proprietary synthetic c3DNA construct has the potential to transform gene therapies, providing cures for unmet medical needs and at a cost enabling global accessibility. In order to efficiently deliver c3DNA to target cells in vivo, Intergalactic is developing innovative delivery platforms using multiple proprietary technologies. This role will actively contribute to process design, development, and optimization for our novel c3DNA manufacturing process.
As a company focused on innovative and accessible solutions for patients, Intergalactic is seeking to hire diverse candidates that bring creativity and new perspectives to our Process Development team.  Strong candidates with any background are encouraged to apply.

  • Lead execution of c3DNA production process for all proof-of-concept and milestone-enabling studies
  • Initiate and drive quality and documentation improvements for c3DNA production process (i.e. writing SOPs, incorporating process controls, etc.)
  • Collaborate with Research, Analytical Development, In Vivo Pharmacology, Engineering and Manufacturing colleagues across Intergalactic to advance c3DNA platform and pipeline
  • Work closely with the Process Development team to actively drive the design, development, and optimization of Intergalactic’s novel c3DNA manufacturing process in order to deliver high purity product at high yields for gene therapy applications
  • Conduct studies to support ongoing process development efforts

Candidate qualifications
  • B.S. in Biological Engineering, Chemical Engineering, or related discipline with 1-3+ years of relevant industry experience in a drug development setting.  Associate’s degrees or alternate degrees with relevant experience are encouraged to apply
  • Experience interfacing with or executing within a GMP manufacturing setting
  • Experience with quality and documentation requirements for GMP-caliber production
  • Proven collaborator and team player
  • Organized, detail-oriented, and a self-starter who continuously seeks innovative solutions
  • Intellectually curious; eager to brainstorm and test potential answers to tough technical questions
  • Works well in a fast-paced startup environment
  • Preferred: Previous use of DoE methods in development
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