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.
#J-18808-LjbffrValidation Engineer - Biopharma & GMP Compliance in irvine at Unknown Company
This position is listed as full time and onsite.