About Us
Evergreen Theragnostics, Inc. is a radiopharmaceutical company headquartered in Springfield, NJ. We operate in a brand-new state-of-the-art facility, developing our own radiopharmaceutical products and providing contract development and manufacturing services for other radiopharmaceutical companies.
We also operate our own cutting edge cancer research laboratories. The company expects rapid growth in the next few years.
Evergreen is a small team, where all team members support each other in a variety of activities. We are looking for team members who are motivated to take on new challenges and excited to help build the company.
Partial equity-based compensation packages possible.
Responsibilities :
- Develop and manage factory schedule for timely manufacturing and testing of radiopharmaceutical drug products.
- Coordinate across multiple departments, including Project Management, Manufacturing, and Quality Control, to understand unique scheduling needs and requirements for all factory projects.
- Follow up with factory personnel to ensure on-time completion of project deliverables.
- Analyze utilization rates for equipment and personnel and assist with factory capacity planning.
- Identify and implement process improvements to achieve and maintain operational efficiency.
- Quickly communicate with management and stakeholders to anticipate and resolve scheduling issues to maintain reliable order fulfilment and prevent delays.
Essential Education and Qualifications :
- 2+ years’ experience in GMP pharmaceutical manufacturing environment or manufacturing resource planning.
- Bachelor’s degree in Business Management, Supply Chain Management, or other related field.
- Strong problem-solving skills and ability to identify opportunities for operational improvements.
- Excellent organizational skills and ability to structure complex topics to manage, prioritize, and schedule multiple projects and deadlines.
- Proficient with project management or resource allocation software and tools.
- Excellent communication skills and ability to coordinate tasks across departments and functions.
- Team-oriented and growth mindset.
- Knowledge of radiopharmaceuticals a plus.
- Knowledge of 21 CFR 11, 21 CFR 211, and 21 CFR 212 regulatory requirements.
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