Principal Biopharma Validation Lead – PPQ & Compliance
Listed on 2026-09-30
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Management
Regulatory Compliance Specialist -
Pharmaceutical
Regulatory Compliance Specialist
Astellas in Massachusetts seeks a Principal Bio Pharma Manufacturing Validation Engineer to lead site validation strategy for facilities, utilities, equipment, computerized systems, and processes, ensuring PPQ readiness and regulatory licensure.
This senior role provides strategic leadership, mentors junior staff, manages budgets and schedules, and drives risk-based validation in support of ongoing commercial supply and inspection readiness.
This is an excellent opening to take on the Principal Biopharma Validation Lead – PPQ & Compliance role at astellas.
This opportunity is part of our work in Bio & Pharmacology & Health, Engineering.
The advertised compensation is 119..
We aim to respond to suitable candidates as soon as possible.
Full responsibilities and requirements are described in the listing above.
Learn more about the Principal Biopharma Validation Lead – PPQ & Compliance role in the description above.
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