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Cambrex

Global CDMO for drug substances

Associate Engineer

Bioprocess & BiomanufacturingConfirmed live in the last 24 hours
Full-timeCharles City, IA, USANo salary listedIn-person

About the Job

Requirements

  • A Bachelor of Science degree in Chemical Engineering or an equivalent degree.
  • A strong understanding of core chemical engineering fundamentals, including thermodynamics, heat transfer, mass transfer, transport, and kinetics.
  • Ability to analyze data from sources including sensors and experiments to identify trends, troubleshoot issues, and improve efficiency.
  • With training and support from senior engineers, identify, analyze, and solve problems related to chemical processes and plant operations, including investigations.
  • Ability to explain technical concepts clearly and accurately to technical and non-technical audiences.
  • Ability to pay close attention to detail to ensure accuracy and quality.
  • Ability to adapt to changing priorities, new technologies, and unexpected challenges.
  • Ability to handle key assignments and meet deadlines with supervision.
  • Ability to wear required personal protective equipment, including steel-toe shoes, safety glasses, and fire-retardant clothing.
  • Physical ability to occasionally lift up to 25 pounds.
  • Ability to regularly sit, stand, bend, reach, and move throughout the facility.
  • Comfort working in a production or laboratory environment with potential exposure to dust, odors, noise, fumes, and varying temperatures.

Responsibilities

  • Rotate through Process, Production, Validation, Project, Environmental, and Reliability engineering roles over an approximate two-year period.
  • Perform scaling calculations for unit operations and assist with conceptual process design.
  • Participate in process reviews for operability, safety, and quality.
  • Support production campaigns through in-person observation.
  • Analyze production and laboratory data to assist with process understanding.
  • Assist with quality investigations and corrective action and preventive action implementation.
  • Support process improvement projects to reduce cycle time, increase yield, and improve quality.
  • Draft manufacturing documents, including process flow diagrams, batch records, validation protocols, standard operating procedures, quality investigations, and campaign reports.
  • Complete special projects in Environmental Engineering.
  • Revise standard operating procedures in Production/Operations Engineering.
  • Troubleshoot operating processes.
  • Update and revise batch records and process setups.
  • Work on process yield or quality improvement projects.
  • Use TrackWise to perform corrective and preventive actions, change controls, and process investigations.
  • Implement small capital projects.
  • Become familiar with maintenance systems, including calibrations, preventive maintenance programs, maintenance planning and supervision, contractor-performed maintenance repairs, capital work completed with internal maintenance labor, and maintenance spare parts inventory.
  • Develop and perform equipment qualification, functional qualification, installation qualification, and operational qualification protocols and reports.
  • Oversee equipment validation and revalidation.
  • Oversee small capital projects and/or Safety Card projects.

About the Company

Cambrex

Global CDMO for drug substances

Cambrex is a global contract development and manufacturing organization (CDMO) that provides drug substance development and manufacturing across the entire drug lifecycle, plus analytical and IND enabling services. It uses a range of specialized technologies—such as continuous flow chemistry, handling of controlled substances, liquid-phase peptide synthesis, solid-state science, material characterization, and production of highly potent APIs—to develop and manufacture drug substances for clients. The company differentiates itself with over 40 years of experience, a staff of about 2,000 experts, and a global footprint in North America and Europe, offering end-to-end capabilities from early development through commercial-scale manufacturing. Its goal is to help clients bring new medicines to market by delivering integrated, reliable drug substance development and manufacturing and related analytical support.

Company size
1,001-5,000
Company stage
IPO
Headquarters
East Rutherford, NJ
Founded
1981

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