Production Scheduler

2 weeks ago


Springfield, Illinois, United States Evergreen Theragnostics Full time

Company Overview

Evergreen Theragnostics, Inc. is a leading radiopharmaceutical firm based in Springfield, NJ. We operate from a modern, advanced facility dedicated to the development of proprietary radiopharmaceutical products and offer contract development and manufacturing services to other companies in the radiopharmaceutical sector. Our organization also features state-of-the-art cancer research laboratories, and we anticipate significant growth in the coming years.

As a compact team, we value collaboration and support among our members in various tasks. We seek individuals who are eager to embrace new challenges and contribute to the growth of the company. Equity-based compensation packages may be available.

Key Responsibilities:

  • Formulate and oversee the production schedule to ensure timely manufacturing and testing of radiopharmaceutical products.
  • Collaborate with various departments, including Project Management, Manufacturing, and Quality Control, to understand the specific scheduling requirements for all production initiatives.
  • Engage with factory personnel to guarantee the on-time completion of project milestones.
  • Evaluate equipment and personnel utilization rates to assist in factory capacity planning.
  • Identify and implement process enhancements to achieve and sustain operational efficiency.
  • Proactively communicate with management and stakeholders to foresee and address scheduling challenges, ensuring reliable order fulfillment and preventing delays.

Required Qualifications:

  • Minimum of 2 years of experience in a GMP pharmaceutical manufacturing setting or manufacturing resource planning.
  • Bachelor's degree in Business Management, Supply Chain Management, or a related field.
  • Strong analytical skills with the ability to pinpoint opportunities for operational enhancements.
  • Exceptional organizational abilities and capacity to manage, prioritize, and schedule multiple projects and deadlines.
  • Proficient in project management or resource allocation software and tools.
  • Outstanding communication skills with the ability to coordinate tasks across various departments and functions.
  • Team-oriented with a growth mindset.
  • Familiarity with radiopharmaceuticals is advantageous.
  • Understanding of 21 CFR §11, 21 CFR §211, and 21 CFR §212 regulatory standards.

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