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Senior Manager, Quality Compliance (Contract)
Bluebird Bio Boston, MA
$152k-190k (estimate)
Full Time | Durable Manufacturing 2 Months Ago
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Bluebird Bio is Hiring a Senior Manager, Quality Compliance (Contract) Near Boston, MA

ABOUT THE FLOCK

The Quality Assurance flock is all about working collaboratively and efficiently, while serving both internal and external customers here at bluebird. Whether it’s ensuring ongoing adherence to process and procedures, driving inspection readiness, or supporting our teams, we are driven by our commitment to quality and regulatory compliance. Come work with an energetic group of birds that loves rising to the challenge much as we love serving our patients! In this contract Quality Compliance role, you will be responsible for vendor related activities including, but not limited to risk assessments, audits, and vendor management.

HOW YOU’LL FLY

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

  • Conducting, reporting, and overseeing vendor audits (e.g., Treatment Centers, CMOs, CTOs, and other GxP vendors).
  • Scheduling, executing, reporting and following-up on external Treatment Center and GMP audits.
  • Documenting and reviewing audit reports to ensure accuracy and adherence to SOP requirements.
  • Ensuring audit observations are communicated, tracked, and remediated in compliance with internal policies as well as with all applicable regulatory requirements.
  • Assisting with the development, maintenance, and execution on the annual audit plan.
  • Compiling program metrics as required.
  • Maintaining the Approved Vendor List.
  • Supporting continuous improvements efforts through the monitoring of metrics.
  • Participating and supporting regulatory inspections. Assisting with inspection readiness efforts.
  • Monitoring industry inspections trends, new/revised regulations, and guidance for impact to operations.
  • Supporting the internal audit program.

WHAT YOU’LL BRING

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

  • B.S. Degree in a science or biopharmaceutical related field.
  • 10 years of experience in GMP and QMS.
  • Direct experience leading and conducting GMP audits, interacting with global vendors, suppliers, and CMOs.
  • Vendor management experience.
  • Experience leading and conducting Treatment Center audits is a plus.
  • Direct experience with Veeva, Trackwise, LIMS, SAP, CMMS, etc.

Contract Length: 9 months

Job Summary

JOB TYPE

Full Time

INDUSTRY

Durable Manufacturing

SALARY

$152k-190k (estimate)

POST DATE

02/26/2024

EXPIRATION DATE

04/25/2024

WEBSITE

bluebirdbio.com

HEADQUARTERS

CAMBRIDGE, MA

SIZE

1,000 - 3,000

FOUNDED

1993

TYPE

Public

CEO

NICK LESCHLY

REVENUE

$200M - $500M

INDUSTRY

Durable Manufacturing

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About Bluebird Bio

bluebird focuses on developing transformative gene therapies for severe genetic diseases and cancer.

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