Quality
Validation Specialist Jobs
Authors and executes validation protocols for GMP equipment, utilities, and processes.
Role overview
Authors and executes validation protocols for GMP equipment, utilities, and processes. The role of a Validation Specialist sits within Quality and is one of the most in-demand positions across pharmaceutical, biotechnology, CRO, and CDMO organizations worldwide.
Required skills
IQ/OQ/PQProtocol Authoring
Education & experience
- Education: Bachelor's in engineering or pharmacy
- Experience: 2–5 years
- Career path: Associate → Senior → Manager → Director within Quality.
Certifications
ISPE CPIP
Salary intelligence
$80,000 – $115,000
Global base salary range (USD, annual)
Entry
$80,000
Mid
$97,500
Senior
$115,000
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