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Manufacturing Operator

Job in Longmont, Boulder County, Colorado, 80502, USA
Listing for: Cambrex Corp.
Full Time position
Listed on 2026-01-10
Job specializations:
  • Manufacturing / Production
    Manufacturing Production, Pharmaceutical Manufacturing, Production Associate / Production Line
Job Description & How to Apply Below
Position: Manufacturing Operator I

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
  • 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!

Job Overview

The Manufacturing Operator will properly operate solid dose manufacturing equipment to perform production of drug products. Personnel in this position will operate manufacturing processing equipment by following standard operations procedures and batch records in accordance with FDA cGMPs. The main focus for personnel in this position will be responsible to operate, set‑up and break down production equipment, clean production areas and maintain consumable supplies.

Responsibilities
  • Properly operates, sets-up and breaks‑down production equipment.
  • Maintains cGMP suites readiness for manufacturing activities including consumable allocation, cleaning of work area and tools and equipment disinfection.
  • Performs minor mechanical maintenance of equipment.
  • Maintains consumable supply inventory.
  • Washes small utensils and glassware for department.
  • Properly performs drug product manufacturing, packaging and labeling activities under direct supervision.
  • Follows written procedures.
  • Distributes clinical supplies.
  • Clearly and accurately documents activities for production records and manufacturing equipment (production notebooks, cleaning logs, maintenance logs, etc)
  • Perform basic math calculations.
  • Assists with batch records for cGMP manufacturing under direct supervision.
  • Other duties as assigned.
Qualifications/Skills
  • Mechanical aptitude is preferred
  • Moderate knowledge of manufacturing equipment for cGMP environment
  • Ability to wear Personal Protective Equipment (PPE). Understands and follows safety procedures and works in a manner to avoid injury to self and co‑workers. Willingness to work with highly toxic and controlled substances.
  • Ability to conduct routine in‑process testing and visual inspections and identify out‑of‑specification conditions.
  • Ability to work in a regulated environment (FDA/DEO/OSHA) and strictly follow procedures.
  • Effectively communicates both verbally and in writing. Ability to read and comprehend detailed written instructions.
  • Ability to clearly and concisely document al work activities in a timely manner utilizing existing forms and records. Writes legibly.
  • Perform basic math functions to include product accountability and material adjustment calculations and rounding. Basic computer skills.
  • Ability to move materials throughout facility using appropriate methods and equipment.
  • Operate machinery and read process control instruments to ensure proper operation. Identify operations problems when they occur.
  • Ability to clean rooms, equipment and tools for use in a cGMP environment.
  • Perform basic troubleshooting applications.
  • Provide basic training to other operators after learning a skill set.
  • Minimal interaction. On an as needed basis.
  • Exhibited leadership skill in individual area of expertise.
  • Must have the ability to work overtime when required.
  • Must adhere to attendance policy of Avista. Expected to arrive for shift…
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