SciPro
Location: On Site in Greater Boston (weekend shifts possible)
Overview We’re partnering with an innovative gene therapy biotech entering a transformative phase as they prepare for their first BLA submission next year. They’re seeking a QC Scientist to play a pivotal role in supporting late-stage quality operations and ensuring analytical readiness.
In this role, you’ll work cross-functionally with both the QC and Analytical Development teams, driving key initiatives that directly impact commercial launch readiness. The ideal candidate will bring prior experience in a fast-paced, GMP-regulated environment and the ability to hit the ground running in a highly collaborative setting.
Qualifications
Hands‑on Quality Control laboratory experience, including method execution, validation, qualification and data review
Strong knowledge of GMP regulations and prior experience working in a cGMP‑compliant environment.
Background in viral vector–based or biologics manufacturing
Proven ability to work cross-functionally in a fast-paced, regulated biotech setting.
Excellent documentation, troubleshooting, and communication skills.
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Overview We’re partnering with an innovative gene therapy biotech entering a transformative phase as they prepare for their first BLA submission next year. They’re seeking a QC Scientist to play a pivotal role in supporting late-stage quality operations and ensuring analytical readiness.
In this role, you’ll work cross-functionally with both the QC and Analytical Development teams, driving key initiatives that directly impact commercial launch readiness. The ideal candidate will bring prior experience in a fast-paced, GMP-regulated environment and the ability to hit the ground running in a highly collaborative setting.
Qualifications
Hands‑on Quality Control laboratory experience, including method execution, validation, qualification and data review
Strong knowledge of GMP regulations and prior experience working in a cGMP‑compliant environment.
Background in viral vector–based or biologics manufacturing
Proven ability to work cross-functionally in a fast-paced, regulated biotech setting.
Excellent documentation, troubleshooting, and communication skills.
#J-18808-Ljbffr