This role is responsible for maintaining, troubleshooting, optimizing, and improving automation systems that support safe, reliable, and compliant pharmaceutical manufacturing operations while supporting the planning, design, execution, commissioning, qualification, and startup of capital projects that enhance manufacturing capabilities, operational reliability, and regulatory compliance. With over 40 years of experience and a team of 2,000 experts servicing global clients from North America and Europe, Cambrex offers a range of specialized drug substance technologies and capabilities, including continuous flow, controlled substances, liquid-phase peptide synthesis, solid-state science, material characterization, and highly potent APIs.