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Cambrex

Global CDMO for drug substances

Production Supervisor

Manufacturing & Production OperationsConfirmed live in the last 24 hours
Full-timeCharles City, IA, USANo salary listedIn-person

About the Job

Requirements

  • Three or more years of chemical processing or manufacturing experience is preferred.
  • Prior supervisory experience is beneficial.
  • Strong written and oral communication skills are required.
  • Strong knowledge of Windows-based software is required.
  • A DEA background check is required.
  • Respirator use is required.
  • A high school diploma or equivalent is required.

Responsibilities

  • Ensure the assigned production area meets or exceeds all safety and quality requirements.
  • Schedule operations to prevent delays and efficiently utilize manpower.
  • Ensure adherence to Standard Operating Procedures in all operations and activities.
  • Ensure employees are properly trained and evaluate their performance.
  • Exercise proper care in the utilization of buildings, equipment, and services.
  • Perform simple laboratory tests on samples of in-process and waste materials to ensure proper operation and equipment function.
  • Coordinate operations with the Maintenance Department to complete scheduled and unscheduled maintenance activities for the operations area.
  • Make recommendations to improve yields and reduce waste, labor, materials, maintenance, handling, and other costs.
  • Initiate investigations of production issues, work with support groups to resolve them, and implement corrective and preventive actions.
  • Work with Process Engineering and Chemical Development during implementation of new products in the manufacturing area.
  • Participate in process evaluations with production superintendents or process engineers as assigned.

Desired Qualifications

  • Three or more years of chemical processing or manufacturing experience.
  • Prior supervisory experience.

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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