Full-Time Sr. Specialist , GMP Quality Assurance – Audit

Job Description

Cubist Pharmaceuticals, Inc. require a “Sr. Specialist , GMP Quality Assurance – Audit” in Lexington, MA:

in science or engineering or equivalent
A minimum of 6 years experience in a biotech or pharmaceutical Quality Assurance environment
Ability to coordinate and…

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Job Categories: Biotech. Job Types: Full-Time.

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