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Sr Director, MSAT

Bedford, NH, USA💼 Full-time🗓 2026-02-10 → 2026-07-31

Core

Acts as a crucial link between client intake, tech transfer, and manufacturing operations to secure present-day operations and deliver future clinical and commercial supply of high-quality drugs.

Role type

Sr Director, Manufacturing Sciences, Analytics, and Technology (MSAT)

Builds

High-quality and innovative drugs for incoming and existing clients across various modalities

Domain

Biopharma / cGMP Manufacturing

Deliverable

production ML models | product features | dashboards & analysis | research | client delivery | infrastructure | physical/clinical work

Required skills

cGMP manufacturing leadership, process improvement, tech transfer management, change management, resource optimization, compliance documentation, aseptic processing expertise, strategic thinking, business acumen, audit support, innovation roadmap development

Preferred skills

Experience leading innovation, extensive industry knowledge, forward-looking technology perspective, complex investigation coordination, gap analysis, risk assessment

Technologies

GMP equipment, aseptic processing systems, manufacturing modalities

Responsibilities

Optimize resource use across the organization for process robustness; Coordinate cross-functional teams for complex investigations and change controls; Oversee authoring of compliance and technical documentation; Assess incoming client projects for compatibility and profitability; Contribute to internal and client audits; Build innovation roadmap between MSAT and Drug Product Manufacturing; Lead client technical intake process; Drive complex change management across functions; Serve as key contact for clients during tech transfer; Act as senior consultant on complex issues

Seniority

Senior Director, strategic leadership & operational oversight

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