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Development:
Senior Process Engineer, Nucleic Acid Process Sciences
Our mission:
Developing curative genome editing treatments that can positively transform the lives of people living with severe and life-threatening diseases.
At Intellia, we are committed to solving the complex challenges of making CRISPR/Cas9-based medicines a reality for patients suffering from genetic diseases and to create novel engineered cell therapies for immuno-oncological and autoimmune diseases.
Intellia is seeking a highly skilled and motivated Sr. Process Engineer to join our Nucleic Acid Process Sciences team.  The successful applicant will have a strong background in scale-up, process development, and manufacture of nucleic acid-based APIs. The candidate will focus on developing and implementing scalable and robust processes related to the enzymatic synthesis of mRNAs. In addition, the role will help lead late-stage process development activities for lead clinical and pre-clinical programs through process robustness/characterization studies, understanding product quality, and helping to refine the product control strategy.  The successful candidate must be able to work in a fast paced and highly dynamic environment.

Responsibilities:

  • Optimization and process limit evaluation of clinical scale mRNA purification using appropriate principals of process optimization (i.e. DoE).
  • Drive mRNA process scale up and development for later stage clinical manufacturing.
  • Lead experiments to confirm robust process performance.
  • Lock the process and define critical process parameters.
  • Explore, develop, and scale-up novel enzymatic processes and nucleic acid purifications
  • Develop MBRs and draft process reports.
  • Provide high quality data and ELN documentation to drive decision making within CMC teams.
  • Communicate research and development findings with internal teams and externally to CDMOs in tech transfer efforts.
  • Operate and maintain multiple laboratory instruments.

Qualifications:

  • Bachelor’s Degree in Biochemistry, Chemical or Biochemical Engineering or related field with 10+ years of industry experience, or MS with at least 7+ years of industry experience. 
  • Able to execute and develop MBRs for mRNA production.
  • Experience in purification and process development for biomacromolecules (e.g. mRNA, DNA).
  • Proficiency with relevant purification and analytical technologies and instrumentation.
  • Experience in process scale up and technical transfer.
  • Proficiency with Design of Experiment and process optimization tools
  • Experience with mRNA purification and in vitro transcription at scale is highly desirable, and GMP experience is a plus.
  • Organized, detail-oriented, and a self-starter who continuously seeks innovative solutions.
  • Team work, versatility, and strong problem solving/analytical skills are required.
  • Excellent verbal and written communication skills.
#LI-KO1
What Intellia Stands For:
We push boundaries. We are focused on positively disrupting health care treatment of patients with genomic diseases. The values we live by and drivers we look for are:
- One is respect for individuals; our unique qualities and strengths; our own ways to understand, learn and improve. One is our single-minded determination to excel; to succeed together. One is you and us – trusting and counting on every single one of us.
- Explore because we seek new ways to tackle disease. Explore with unbounded minds…free from assumptions, open to ideas. Explore by staying curious, by pushing boundaries, overcoming obstacles. Explore means thinking of new ways.
- Disrupt by thinking courageously…and creating a better future. Disrupt by defying conformity; interrogating the status quo; questioning our momentum. Disrupt with challenging thoughts…with that breed of skepticism that shows you have better solutions.
- Deliver with your focus on the objective and your determination to complete the task. Deliver by advancing relentlessly and by maintaining high standards…even when nobody is watching. Deliver by staying accountable and pulling your weight. Deliver because patients are counting on us to make the promise reality. Get it done.
POSITION: Full-Time, Exempt
EEOC Statement: Intellia believes in a diverse environment, and is committed to equal employment opportunity for all its employees and qualified applicants. We do not discriminate in recruitment, hiring, training, promotion or any other employment practices for reasons of race, color, religion, gender, national origin, age, sexual orientation, marital or veteran status, disability, or any other legally protected status. Intellia will make reasonable accommodations for qualified individuals with known disabilities, in accordance with applicable law.
Intellia’s web-based application process is managed through Lever. Information submitted through application forms is collected by Lever and subject to Lever’s privacy policy.
EEOC Statement: Intellia believes in a diverse environment, and is committed to equal employment opportunity for all its employees and qualified applicants. We do not discriminate in recruitment, hiring, training, promotion or any other employment practices for reasons of race, color, religion, gender, national origin, age, sexual orientation, marital or veteran status, disability, or any other legally protected status. Intellia will make reasonable accommodations for qualified individuals with known disabilities, in accordance with applicable law.
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