Program Manager

Made Scientific, Inc.

Princeton (NJ)

On-site

USD 100,000 - 140,000

Full time

14 days+

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Job summary

Made Scientific, Inc. seeks a Program Manager in Princeton, NJ to oversee complex CDMO programs. You will own schedules, budgets, and client communications, integrating contracted scope into the project plan and coordinating cross-functional teams for successful completion.

The role emphasizes proactive risk management, stakeholder management, and continuous improvement of PMO practices to support clinical and commercial supply pipelines.

Qualifications

  • 1–3 years of experience in the pharmaceutical/biotech industry, with exposure to CDMO operations.
  • Bachelor’s degree in Engineering, Science, or related discipline.
  • Proficiency in project management tools (e.g., Smartsheet).
  • Experience supporting customer programs from development through clinical manufacturing and release.

Responsibilities

  • Lead project management with emphasis on timeline/critical path, risk, and budget management.
  • Provide proactive client communication through presentations and 1:1 interactions.
  • Plan projects end-to-end using management tools from initiation to closure.
  • Drive cross-functional accountability to meet deliverables, timelines, and revenue goals.
  • Develop enterprise-wide tools, systems, and processes including change management.

Skills

Project management
Client communication
Cross-functional teamwork
Budget management
Schedule planning

Education

Bachelor's degree in Engineering/Science

Tools

Smartsheet
Microsoft Project

Job description

About Made Scientific

Made Scientific is a leading US-based cell therapy contract development and manufacturing organization (CDMO) specializing in the development, manufacturing, and release of autologous and allogeneic cell therapy products for clinical-and-commercial supply. Made Scientific combines the agility and entrepreneurial spirit of a specialist CDMO with the global expertise and resources of GC Corporation of South Korea, a global leader in the pharmaceutical and biotechnology sectors.

About Made Scientific

Made Scientific is a leading US-based cell therapy contract development and manufacturing organization (CDMO) specializing in the development, manufacturing, and release of autologous and allogeneic cell therapy products for clinical-and-commercial supply. Made Scientific combines the agility and entrepreneurial spirit of a specialist CDMO with the global expertise and resources of GC Corporation of South Korea, a global leader in the pharmaceutical and biotechnology sectors.

Position Summary

The Program Manager (PgM) is responsible for overseeing and leading the successful execution of complex projects while collaborating with cross-functional teams and stakeholders to track program progress and mitigate potential risks. The PgM will drive and own the creation, maintenance, and oversight of project schedules, manage project budgets, and will serve as the primary point of contact with our clients and internal stakeholders. It is the PgM’s role to integrate contracted scope into the project plan and communicate this information to all members of the cross-functional team. This scope includes the management of both customer and enterprise programs. The PgM will also play a key role in implementing the vision of the future state of the PMO by leveraging their previous experience to develop best practices across the organization.

Key Responsibilities
  • Lead by example in utilizing best practices in project management, specifically in the areas of timeline/critical path management, risk management, and budget management
  • Demonstrate excellence in proactive client communication through both formal presentations and informal 1:1 interactions, building trustworthy relationships
  • Conduct detailed end-to-end program planning with project management tools (e.g., Smartsheet, Microsoft Project) from initiation through closure
  • Drive accountability within cross-functional teams to meet deliverables, timelines, and business (revenue) goals
  • Develop and implement enterprise-wide tools, systems, and processes, including driving training and change management
  • Ensure dissemination of approved work scope to team members
  • Provide project management leadership to cross-functional teams to ensure successful execution of project scope
  • Manage client and stakeholder relationships, communications, requirements, and expectations
  • Anticipate and proactively manage changes in project scope through the change order process
  • Ensure excellent communication within the team, to site leadership, relevant stakeholders, and to clients
  • Serve as primary point of contact with the client post-signature, in partnership with Sales & BD
  • Prepare and conduct program reviews and presentations across internal teams, clients, and senior management
  • Coordinate development of subcontractor Statements of Objectives and Statements of Work
  • Maintain project lessons learned and best practices, ensuring dissemination within the PMO and functional leadership
  • Apply financial acumen in developing revenue forecasting models
  • Assist with new business proposal preparation as required
  • Manage project risk registers and implement mitigation strategies as appropriate
  • Perform other duties as assigned by the Head of Portfolio and Program Management
Required Qualifications
  • 1–3 years of experience in the pharmaceutical/biotech industry, with exposure to CDMO operations
  • Bachelor’s degree in Engineering, Science, or related discipline
  • Proficiency in project management tools (e.g., Smartsheet)
  • Experience supporting customer programs from development through clinical manufacturing and release
  • Strong financial acumen with understanding of CDMO business needs
  • Familiarity with time-tracking tools, processes, and systems
  • Excellent organizational, interpersonal, and communication skills
Preferred Qualifications
  • Experience in cell therapy modalities
  • PMP certification
Equal Employment Opportunity Statement

Made Scientific is proud to be an Equal Opportunity Employer committed to fostering a diverse and inclusive workplace. We make employment decisions based on qualifications, merit, business needs, and job requirements without regard to race, color, religion, creed, sex, pregnancy, childbirth or related medical conditions, sexual orientation, gender identity or expression, national origin, ancestry, age, disability, genetic information, marital status, military or veteran status, citizenship status, or any other status protected by applicable federal, state, or local law. Made Scientific is committed to providing reasonable accommodations to qualified individuals with disabilities and to applicants and employees with sincerely held religious beliefs, practices, or observances, unless doing so would create an undue hardship.

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