Program Manager

2 weeks ago

College Station, Texas, United States Fujifilm Corporation Full time
Job Title: Program Manager

At Fujifilm Diosynth Biotechnologies, we are seeking a highly skilled and experienced Program Manager to join our team. As a Program Manager, you will be responsible for the planning and delivery of programs from contract signature to program closure, ensuring alignment with contractual commitments and the company's vision and mission.

Key Responsibilities:
  • Onboard new customer programs with the Sales Team and transition to become the primary liaison for program planning and execution.
  • Lead the planning and execution of programs in alignment with FDBT's Program Management business best practice.
  • Oversee the general day-to-day execution of Program activities and planning to ensure on-time completion of Program tasks and deliverables.
  • Identify program delivery risks and mitigations and ensure the program team, site leadership team, and customer are appropriately informed.
  • Lead the Program team in Stage Gate reviews to communicate program readiness and risk profile to the site leadership team.
  • Attend and lead daily Tier 2 and Tier 3 meetings to support FDBT's communication structure for escalations and feedback in program risk items.
  • Ensure financial activities and program milestones are aligned, including SOW, PPS, revenue recognition milestones, change orders, invoicing/payment activities, etc.
  • Ensure all Contract elements are completed with support from Head of Program Management.
  • Develop and maintain the Master Program Plan (MPP) including ensuring durations and accountabilities for all revenue generating milestones are accurate through the scope of the program.
  • Collaborate with the Sales Team to identify additional opportunities for additional work within the current contract.
  • Partner with functional teams to ensure that MPP revenue generating milestones are accurately translated into functional deliverables and all action items are completed per the committed timeline.
  • Work closely with Process Development, Manufacturing, Engineering, Quality Control, and Quality Assurance to reduce time to clinic or market, improve ease of manufacturing, and reduce costs while achieving and maintaining full compliance.
  • Accurately define timelines and resource requirements for the assigned Programs.
  • Maintain Program documentation, including change orders, Program reports, timelines, etc.
  • Manage and lead Program team meetings, including issuance of agenda, action items, meeting minutes, client communications, etc.
  • Communicate Program updates to the Leadership Team at predefined milestones and at defined intervals.
  • Organize and conduct Program team and Joint Steering team meetings with external clients, including agenda, meeting notes, action items, and follow-up of action items.
  • Track and report program performance, including financial, delivery metrics, and analysis, monthly reports, quarterly and annual leadership reviews, revenue change log, etc.
  • Responsible for authoring Scopes of Work, Change Orders, Cost Models, and Confidentiality Agreements. Responsible for approving Program purchase orders. Responsible for forecasting revenue and reviewing/approving monthly customer invoices.
  • Continuous improvement of existing systems as well as implementation of new program management systems, including training of employees to ensure FDBT maintains best practices in the industry.
Requirements:
  • Bachelor's Degree in Business, Engineering, Microbiology, Chemistry, Biochemistry, or related field preferred with 4+ years' relevant project experience.
  • High School Diploma or equivalent and 2+ years' experience in Project Management with Fujifilm Diosynth Biotechnologies or a similar CDMO or biotechnology company.
  • Relevant project management experience in a biotechnology or pharmaceutical development and manufacturing environment managing one or more projects of medium to high complexity preferred.
  • Certifications in Project/Risk Management or Lean Six Sigma preferred.
  • Experience in a cGMP facility or working with FDA regulations preferred.
  • Previous Accounting/Finance/Budgeting experience preferred.
  • Excellent attention to detail with strong organizational and analytical skills.
  • Computer proficiency required, including strong experience with Microsoft Office (Word, Excel, PowerPoint).
  • Excellent problem-solving and conflict resolution skills and the ability to identify, assess, and resolve business problems, issues, risks, and facilitate issue resolution and risk mitigation.
  • Ability to accurately complete required documentation.
  • Good written and oral communication skills and the ability to effectively interact with all levels of the organization.
  • Excellent time management skills with the ability to multi-task and self-manage activities.
  • Effective resource and Program planning/decision making.
  • Experience with problem-solving and conflict resolution.
  • Accountable for all aspects of Program Team's data support, entry, and ongoing data accuracy reporting.
  • Knowledgeable in Quality systems, tools for process improvement, and cGMP guidelines.
  • Role model for company core values of trust, delighting our customers, Gemba, and Genki.
Physical Requirements:

The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

  • Experience prolonged sitting, standing, walking, bending, stooping, and stretching.
  • Use hand-eye coordination and manual dexterity sufficient to operate a keyboard, photocopier, telephone, calculator, and other office equipment is required.
  • Attendance is mandatory.

We are a company of emboldened goal seekers – driven by an innate desire to better ourselves, our families, our workplace, our company, our community, and the world at large.

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