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Cambrex

Global CDMO for drug substances

Production Superintendent

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

About the Job

Requirements

  • At least four years of chemical processing or manufacturing experience; prior supervisory experience is preferred.
  • A high school diploma or equivalent and a bachelor's degree in Chemistry or Chemical Engineering are required.
  • Sound written and oral communication skills.
  • Ability to conduct employee training and presentations and actively participate in regulatory and customer audits.
  • Strong leadership skills.
  • Financial knowledge relevant to manufacturing.
  • Strong computer knowledge in Windows-based software, including Microsoft Word, Excel, and PowerPoint.
  • Ability to obtain DEA clearance for drug manufacture.
  • Respirator use is required.

Responsibilities

  • Manage assigned production work centers or facilities to meet customer and business demands while maintaining regulatory compliance and company standards.
  • Develop, direct, and guide production supervisors, production engineers, and plant operators while meeting manufacturing schedules.
  • Lead and promote safety, environmental awareness, quality, cost savings, and compliance with regulatory programs.
  • Provide interdepartmental and intradepartmental technical assistance to facilitate company growth.
  • Work with all departments to ensure timely shipment of quality products and meet or exceed customer expectations.
  • Ensure assigned production areas meet or exceed safety and quality requirements.
  • Schedule operations and maintenance to prevent delays and use manpower efficiently.
  • Ensure adherence to Standard Operating Procedures in all operations and activities.
  • Work with production supervisors to ensure employees are properly trained and evaluate their performance.
  • Use buildings, equipment, and services with proper care.
  • Identify and implement process improvements affecting yield, throughput, waste, labor, raw materials, product quality, and cycle time.
  • Investigate operational issues, work with support groups to resolve them, and implement corrective and preventive actions.
  • Work with Process Engineering and Chemical Development to implement new products in manufacturing.
  • Participate in process or capital project evaluations as assigned.
  • Coach production supervisors and their subordinates on company policies and procedures; conduct training based on employee and company needs; guide employees to increase their understanding and knowledge of plant operations; and identify and promote activities that enhance the work environment.

Desired Qualifications

  • Prior supervisory experience.
  • An MBA or MS in Chemistry or Chemical Engineering.

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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