Director, Project Management, CDMO
3 weeks ago
Director, Project Management, CDMO
About Us
Evergreen Theragnostics, Inc. is a radiopharmaceutical company beginning operations in Springfield, NJ. The state-of-the-art facility will provide contract development and manufacturing services for radiopharmaceutical companies, including therapeutics and centrally distributed diagnostics. The company expects continued 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:
- Complete tech transfers on time with high quality results, measured by customer satisfaction and successful IND filings.
- Generate and forecast CDMO revenue and grow customer base.
- Build and generate contracts, delegate to project management team as necessary.
- Ensure successful customer/regulatory audits for CDMO business.
- Establish consistent and reliable isotope supply with numerous suppliers.
- Manage clinical doses for first CDMO projects with >99% successful delivery.
- Oversee project managers on maintaining CDMO client relationships throughout the project lifecycle from onboarding through clinical supply.
- Hire, train, develop, and manage Project Management and Supply Chain teams.
- Procure and manage all external CDMO vendors, delegating as necessary.
- Manage CDMO budget and forecasting.
Essential Education and Qualifications:
- Bachelor’s Degree in Chemistry or Biochemistry and a minimum of 5 years of applicable GMP laboratory experience required. Radiopharmaceutical experience preferred.
- MBA preferred.
- Excellent oral and written communication, organizational, and problem-solving skills while working under strict timelines.
- Management or supervisory experience preferred.
- Ability to convey complex ideas in a simple manner to management and customers, exercise independent judgement during method development/transfer processes.
- Knowledge of analytical methods currently used for testing, release, and stability of sterile pharmaceutical products.
- Team oriented mindset and demonstrates ability to work easily with cross functional teams.
- Fluent in Microsoft Word and experienced in working with laboratory information management systems (LIMS).
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