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Location
In office (Charles City)
Seniority
Middle · 3+ years exp

Confirmed on the employer's own hiring board on Nov 6, 2026. First seen by Alion on Nov 4, 2026.

Overview
Company
Impact
Profile match
Cambrex is a global contract development and manufacturing organization (CDMO) offering drug substance, drug product and analytical services.

Company Information

You Matter to Cambrex.

Cambrex is a leading global contract development and manufacturing organization (CDMO) that provides drug substance, drug product, and analytical services across the entire drug lifecycle. With more than 40 years of experience and a growing team of over 2,000 professionals servicing global clients, Cambrex is a trusted partner in branded and generic markets for API and dosage form development and manufacturing.

Your Work Matters.

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!

Your Future Matters.

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!

Overview:

Reporting to the shift supervisor, the Reactor Operator will be expected to successfully produce chemical and pharmaceutical products in our manufacturing environment.

Responsibilities:

Operate batch and continuous type reactors, high pressure reactors, centrifuges, filters, solvent distillation equipment and supporting equipment involved in testing, all according to designated procedures.

 Monitor the equipment; setting controls on valves, vacuums, pumps, pressures, etc., according to designated procedures to achieve desired results.

 Monitors the process variables and makes process control adjustments to maintain the proper process control. Use manual and computer-controlled devices to monitor and control the process.

 Clean all equipment used (boil, scrape or scrub out) following designated procedures.

 Assist in training new Pharma Reactor Operators.

 Drum compounds and hazardous waste; label according to set standards; transport to assigned areas.

 Assure area is kept clean and all precautions are taken to prevent environmental spills and control discharge to WWTP at acceptable limits.

 Interpret results and monitor processes using computer-controlled devices.

 Responsible for safe handling of hazardous materials including loading/unloading trucks, processing, packaging and cleanup of equipment.

 Responsible for completion of all operation log books in Pharma area.

 Troubleshoot production line and equipment problems in a safe and effective manner.

 Assist lab personnel with implementing new processes or process changes

 Complete line entry, confined space, and hot work permits. 

 Assist in writing and updating process procedures and SOP’s.

 Adhere to all EPA, FDA and cGMP regulations as they relate to the operation of the chemical production facility.

 Take samples for in-process and Quality Control analysis.

 Perform laboratory tests on process samples and act on results.

 Assume duties of Reactor Operator Chem I/II

Qualifications / Skills:

  • Good communication skills, both oral and written
  • Strong mechanical aptitude/knowledge

Education, Experience, and Licensing Requirements: (Text Only)

- High School Diploma or equivalent - 3 or more years of experience in a manufacturing environment or related business
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