Scientific Manufacturing Operator

Company Information

You Matter to Cambrex.

Cambrex is a leading global contract development and manufacturing organization (CDMO) that provides drug substance development and manufacturing across the entire drug lifecycle, as well as comprehensive analytical and IND enabling services.

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.

At Cambrex, we strive to build a culture where all colleagues have the opportunity to:

• engage in work that matters to our customers and the patients they serve
• learn new skills and enjoy new experiences in an engaging and safe environment
• strengthen connections with coworkers and the community

We’re committed to attracting and nurturing a passionate team of valued professionals in our fast-paced and growing company. We offer a competitive benefits package that includes healthcare, life insurance, planning for retirement, and more!

Known for our customer-focused scientific and manufacturing excellence, as well as our strong commitment to quality and safety, we offer a range of career and growth opportunities across our global network of locations. Together with our customers, we aim to improve the quality of life for patients around the world. Start a career where You Matter by applying today!

Reporting to the Shift Supervisor, the Scientific Manufacturing Operator is responsible for safely operating and monitoring pharmaceutical manufacturing equipment used in the production of active pharmaceutical ingredients (APIs) and pharmaceutical intermediates. This role combines scientific knowledge with hands‑on manufacturing operations in a current Good Manufacturing Practice (cGMP)-regulated environment.

The Scientific Manufacturing Operator will operate reactors and supporting process equipment, perform in-process testing, monitor production parameters, troubleshoot equipment and process issues, and ensure all activities are documented in accordance with cGMP requirements.

This is a career-entry scientific manufacturing role that provides recent graduates with an opportunity to apply their scientific or engineering education in a large-scale pharmaceutical manufacturing environment while developing technical expertise in API manufacturing processes.

• Operate batch and continuous reactors, centrifuges, filters, solvent distillation equipment, dryers, and supporting process equipment in accordance with approved procedures.
• Execute manufacturing activities in accordance with batch records, standard operating procedures (SOPs), safety requirements, and cGMP regulations.
• Monitor and control process variables, including temperatures, pressures, flows, vacuum systems, reaction conditions, and other critical process parameters.
• Utilize computerized control systems and manufacturing software to monitor and operate pharmaceutical production processes.
• Perform routine in-process sampling and analytical testing to monitor production quality and process performance.
• Interpret analytical and process data and make appropriate operational adjustments within established procedures and operating parameters.
• Troubleshoot equipment and process issues in a safe and effective manner and elevate issues as appropriate.
• Complete equipment setup, cleaning, inspection, and changeover activities in accordance with approved procedures.
• Assist with the implementation of new manufacturing processes, process improvements, technology transfers,…