ABOUT THE NEST

The nest is a place where every role has meaning, every team member is respected, and every day is a chance to fly higher. When you join bluebird bio, you're not just landing a new gig, you become part of a flock that's pursuing curative gene therapies to give patients and their families more bluebird days. We are doers, thinkers and collaborators who embrace and live by our values:

  • Persist for Purpose
  • Be Compassionate
  • Stay humble and curious
  • Keep it real
  • Celebrate (sm)all wins

Our innovation is rooted in the diversity of our teams and results are achieved through cooperation and the integration of multiple viewpoints. This is personal and we approach every challenge with radical care.

 

 HOW YOU’LL FLY

This is a hands-on role within Quality Control (QC) Operations, reporting to the Director of QC Operations. In this role, you will provide a significant contribution to the daily operations within Quality Control. You will partner with various internal laboratory operations as well as our Contract Testing Organizations (CTO) network. A normal day will include supporting all activities associated with testing at CTOs from sample submission to Certificate of Analysis (COA) approval. Additionally, you will provide valuable support in investigating any anomalous or out-of-specification results and/or driving QC document improvements through bluebird bio’s quality system.

You'll help to bring more patients their bluebird days by: 

  • Compiling, reviewing, and archiving CTO data and test records in support of COA generation
  • Inputting lot and test data into QC trackers
  • Scheduling sample shipments
  • Owning and/or supporting testing related deviations, laboratory investigations, CAPAs and out-of-specification (OOS) results
  • Supporting document revisions related to method lifecycle and analytical method implementation
  • Tracking & trending QC metrics

 

WHAT YOU’LL BRING

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

  • BS in a scientific discipline and 3+ years of related experience in QC GMP environment in a clinical and/or commercial environment
  • Highly collaborative team player with experience being part of a team and working cross functionally
  • Excellent organizational skills with an ability to navigate software and tools such as Veeva and Excel spreadsheets
  • Experience with CTO/CMO interaction preferred

 

Contract Length: 12 months

Location: Remote (East coast based) or MA hybrid.

 

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.

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