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Cambrex

Global CDMO for drug substances

Reliability Technician

Mechanical Maintenance and Reliability EngineeringConfirmed live in the last 24 hours
Full-timeCharles City, IA, USANo salary listedIn-person

About the Job

Requirements

  • A high school diploma is required.
  • The candidate must have, or be willing to obtain, Machinery Lubrication Technician 1, Ultrasonic Level 1, Basic Vibration Level 1, Thermography Level 1, Yellow Belt Lean Six Sigma, and Certified Maintenance and Reliability Professional (CMRP) certifications.
  • Strong aptitude in mechanical and electrical systems is required.
  • Working knowledge of Microsoft computer applications in a Windows-based environment is required.
  • High attention to detail is required.

Responsibilities

  • Collect oil samples according to the oil sample test plan and perform oil changes based on the results.
  • Perform routine ultrasonic greasing and collect data for all critical equipment.
  • Conduct routine air and nitrogen leak surveys and oversee necessary repairs.
  • Collect routine vibration data for all identified equipment.
  • Conduct yearly digital thermography of all motor control center panels.
  • Work with the Reliability Engineer to collect data supporting failure analyses.
  • Participate in criticality assessments and failure mode and effects analyses as required.
  • Collect data supporting the Mechanical Integrity program and facilitate required repairs.
  • Create notifications and work orders in SAP.
  • Perform other duties as assigned.

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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