Senior Drug Product Process Scientist, Small Molecule

Takeda Pharmaceutical Co.; Boston (MA); Vor Ort; USD 137.000 - 215.000; Vollzeit

Zusammenfassung

Takeda Pharmaceutical Co. seeks a Drug Product Process Scientist - Small Molecule at Sr. Manager level in Cambridge, MA.

You will serve as the accountable technical owner and strategic leader for assigned drug product portfolios, ensuring supply continuity, launch readiness, lifecycle excellence, and regulatory compliance across networks. Responsibilities include leading complex technical programs, technology transfers, validation, process optimization, and cross-functional execution with

Qualifikationen

• Ph.D./MS/BS in chemical engineering, pharmaceutical sciences, chemistry, biology or related field.
• 10–20 years of pharmaceutical/biotech experience with leadership roles.
• Experience leading drug product manufacturing, tech transfer, validation, and lifecycle management.
• Experience across global manufacturing networks including internal sites and CMOs.

Aufgaben

• Lead complex technical programs with cross-functional dependencies to meet quality, cost, and supply goals.
• Drive process robustness, yield, compliance, and operational performance improvements.
• Act as accountable technical owner for products, networks, or major workstreams.
• Lead cross-functional execution across Manufacturing, Quality, Regulatory Affairs, and Supply Chain.
• Define and implement manufacturing, sourcing, transfer, validation, and network strategies.
• Mentor teams and provide data-driven recommendations to senior stakeholders.

Kenntnisse

Leadership

Cross-functional leadership

Program management

Regulatory CMC

Tech transfer

Process optimization

GMP compliance

Ausbildung

PhD in Chemical Engineering

MS in Pharmaceutical Sciences

BS in Chemistry

Jobbeschreibung

Takeda Pharmaceutical Co. seeks a Drug Product Process Scientist - Small Molecule at Sr. Manager level in Cambridge, MA.

You will serve as the accountable technical owner and strategic leader for assigned drug product portfolios, ensuring supply continuity, launch readiness, lifecycle excellence, and regulatory compliance across networks. Responsibilities include leading complex technical programs, technology transfers, validation, process optimization, and cross-functional execution with