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The Process Engineer II will design and develop new equipment, evaluate technologies, assist with project integration, and support regulatory submissions in a biopharmaceutical environment.

The VP of Business Development oversees regional sales, drives growth, maintains client relationships, leads teams, and collaborates across departments.

The Principal Process Engineer leads technology transfer and validation for clinical and commercial biologics manufacturing, ensuring compliance and process optimization.

The Quality Risk Manager ensures compliance with quality systems, manages site risk registers, coordinates risk assessments, and provides guidance on risk mitigation strategies.

Lead global MSAT technology transfer and process validation for late-stage and commercial biologics. Drive site-to-site transfers, develop global templates/protocols (PPQ, PQ, batch records), perform gap/risk analyses and mitigation, analyze process data and annual reviews, support regulatory CMC documentation and inspections, and mentor junior engineers.