CDMO Project Manager

job
  • Evergreen Theragnostics
Job Summary
Location
Springfield ,NJ 07081
Job Type
Contract
Visa
Any Valid Visa
Salary
PayRate
Qualification
BCA
Experience
2Years - 10Years
Posted
21 Nov 2024
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Job Description

Project Manager – CDMO


*FULL TIME ON-SITE POSITION, PLEASE DO NOT APPLY IF YOU ARE LOOKING FOR HYBRID OR REMOTE*


About Us


Evergreen Theragnostics, Inc. is a radiopharmaceutical company headquartered in Springfield, NJ. We operate in a brand-new state-of-the-art facility, providing contract development and manufacturing services for radiopharmaceutical companies, including therapeutics and centrally distributed diagnostics. We also operate our own cutting edge cancer research laboratories, developing proprietary, radiotherapeutic medicines. 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:

  • Lead the manufacturing and CMC development projects from kickoff through tech transfer and process optimization, until handoff to production team
  • Develop and Execute project plans and budgets, under the supervision of VP, CDMO Project Management.
  • Assist in tech transfer and/or development of any Standard Operating Procedures (SOPs) and other documentation relating to these projects.
  • Participate in initial radiolabeling, QC testing, and troubleshooting for new products.
  • Manage training and internal hand-off of projects to production and quality teams.
  • Maintain standard project management tools including open issue lists and Gantt charts.
  • Collaborate closely with client teams as well as internal departments (production, quality, finance).


Qualifications:

  • Must have either 3-4 years’ experience in radiopharmaceuticals industry and/or 2-3 years project management experience in other segments of pharmaceutical industry. Must have experience working in a GMP environment.
  • Minimum bachelor’s degree in a technical discipline (Chemistry, Engineering, etc.), advanced scientific degree strongly preferred.
  • Self-starter with strong problem-solving skills and ability to work under strict timelines.
  • Demonstrated ability to work independently, and to exercise judgement during method development/transfer processes.
  • Team-oriented mindset and demonstrates ability to work easily with cross functional teams.
  • Practical and/or curriculum-based experience with basic project management techniques and software applications.
  • Ability to convey complex ideas in a simple manner to management and customers.
  • Fluent in Microsoft Office suite (Word, Excel, Project, etc.) and experienced in working with laboratory information management systems (LIMS).
  • Excellent communication skills.
  • Excellent technical writing skills.

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