Engineering

Validation Engineer - Biopharma & GMP Compliance

Cryoport Systems

Irvine · Canada · United States

Cryoport Systems is seeking support for Consulting Services qualification activities in the life sciences supply chain. You will help develop validation procedures, prepare equipment, and document test results while coordinating with internal teams and external testing labs.

Responsibilities include creating project plans for shipping lane qualifications, packaging configurations, and qualification testing. Strong communication and meticulous documentation are essential to drive client success.

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Reference: WJ-5385_3077394

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