Uncubed
   

Quality Control Analyst (Contract)

Bluebird Bio, Cambridge, Massachusetts, United States

integrated product platforms with broad therapeutic potential

Duration: Contract


On January 11, 2021, we announced our intent to separate our severe genetic disease and oncology businesses into differentiated and independent publicly traded companies. We will retain focus on severe genetic disease (SGD) and will launch our oncology business (“Oncology Newco”) as a new entity, with the completed transition expected by the end of 2021.

 

ABOUT THE NEST

At bluebird, only two things matter - patients and our people. When you join the nest, you're not just landing a new gig, you become a part of a flock that's soaring to new heights. We’re 1100+ doers, thinkers and collaborators across the globe with a strong sense of our values and our purpose. Our innovation and sustainability are rooted in the diversity of our teams and results are achieved through cooperation and the incorporation of multiple points of view. This is personal and we approach every challenge with radical care. The time is now to rise up and recode the science, the systems, and the status quo.

Quality Control Analyst (Contract)

This role is for a 12-month contract position.

 

ABOUT THE FLOCK

The Quality Control flock is all about getting stuff done and working collaboratively. Whether it’s making sure we’re supporting establishing new commercial-level GMP testing laboratories for release and stability for multiple stages of our gene therapy products, working collaboratively across the nest, or driving innovation as a unit, we are driven by effective communication, critical thinking, and the ability to ask questions while supporting one another. Come work with an energetic and enthusiastic group of birds that loves rising to the challenge much as we do!

HOW YOU’LL FLY

As a Quality Control Analyst bird reporting to Hopa Knight, you'll help to bring more patients their bluebird days by:

  • Perform cGMP analytical testing (pH, osmolality, appearance, bioassay, cell culture, flow cytometry, qPCR, and ELISA)
  • Review and evaluate raw data (peer review level)
  • Author SOPs/Forms, technical reports, and equipment validations with guidance
  • Initiate laboratory deviations and support investigations (IA, OOS, AR), performing assessment, authoring protocols/reports and investigation closure with guidance
  • Support operational systems (equipment/instrument maintenance/calibration, equipment alarm monitoring, sample handling/tracking, data integrity/control, cGMP documentation, LIMS, laboratory audit, and method training)
  • Execute phase-appropriate test method validation protocols as needed
  • Support CAPA/Continuous Improvement Initiatives
  • Other related tasks as needed

WHAT YOU’LL BRING

You’re the bird we’re looking for if you:

  • BS with 4 – 7+ years in a biotechnology discipline or MS 2 – 4+ years
  • 4 – 7+ years of experience in a cGMP/GxP environment is preferred
  • Preferable hands-on experience in cell culture, flow cytometry, quantitative PCR, and other bioanalytical methods such as ELISA
  • Superb organizational, analytical, and communications skills and “do-what-it-takes” attitude
  • Self-directed individual who is able to work with limited direction in a fast-paced, goal-oriented environment

All our birds embrace the principles of the bluebird bio culture:  b colorful, b cooperative, b yourself.

bluebird bio is deeply committed to fostering an environment where diversity and inclusion are not only valued, but prioritized. We believe a diverse and inclusive community empowers us to act courageously, care deeply, and dream boldly to impact people in big ways.  Diverse viewpoints bring diverse capabilities which strengthen our focus and fuel our growth.

bluebird is proud to be an equal opportunity employer, seeking to create a welcoming and diverse environment.  All applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, veteran status or any other applicable legally protected characteristics.

About Bluebird Bio

About us We are leading the gene therapy revolution. Our integrated product platforms encompass gene therapy, cancer immunotherapy and gene editing – providing us with the potential to treat, and hopefully cure, a broad range of serious diseases. We have a lot of energy, and it’s not just the abundance of coffee that keeps us going. Find out what sparks our excitement and inspires us every day.

Want to learn more about Bluebird Bio? Visit Bluebird Bio's website.