Summary:  The Associate Program Director, with mentoring and support from the Head of Program Management and/or a Program Director, will be responsible for the planning and delivery of programs from the point of contract signature (Scope of Work/Letter of Intent/Contract) to program delivery including technology transfer and taking a product/process from execution of a client commercial agreement or memorandum of understanding through process development and early stage clinical supply through program closure.  The Associate Program Director ensures the organization provides services in alignment with contractual commitments to the clients and the Company’s vision/mission (strategy and compliance).  

The work we do at FUJIFILM Biotechnologies Texas has never been more important—and we are looking for passionate, mission-driven people like you who want to make a real difference in people’s lives. 

From developing the next vaccine to advancing cell and gene therapies, we collaborate with industry leaders to tackle complex challenges and deliver meaningful solutions.

If you’re ready to help transform the future of medicine, join FUJIFILM Biotechnologies. We offer a flexible work environment and we’re proud to cultivate a culture that will fuel your passion, energy, and drive—what we call Genki. 

Our state-of-the-art biomanufacturing facility is located in in College Station, Texas, which combines a small-town feel with vibrant culture, top-notch schools, and close proximity to big city life. Nestled between major hubs, it’s a dynamic location that blends convenience with innovation.

Fujifilm is globally headquartered in Tokyo with over 70,000 employees across four key business segments of healthcare, electronics, business innovation, and imaging. We are guided and united by our Group Purpose of “giving our world more smiles.” Visit: https://www.fujifilm.com/us/en/about/region/careers

Essential Functions: 

• On board new customer programs with the Commercial Team to transition to become the primary liaison for program planning and execution upon confirmation that a Verbal Win/Letter of Intent has been reached. 

• Lead the planning and execution of programs in alignment with the FLBT Program Management business best practice (vision, mission, strategy-goals-objectives). 

• Oversee the general day-to-day execution of program activities and planning to ensure on-time completion of program tasks and deliverables as scheduled.  

• Identify program delivery risks and mitigations and ensure the program team, the site leadership team, and the customer are appropriately informed. 

• Lead the program team in Stage Gate reviews as part of the program life cycle to communicate program readiness and risk profile to the site leadership team. 

• Attend and lead regular Tier meetings to support FLBT’s communication structure for escalations and feedback in program risk items. 

• Serve as the lead with the functional areas to ensure the SOW elements are accurate, complete, and organized based on revenue generating segments of work.  

• Ensure financial activities and program milestones are aligned (SOW, revenue recognition milestones, change orders, invoicing/payment activities, etc.). 

• Ensure all Contract elements (MSA, Quality Agreement, Price and Payment Schedule, SOW etc) are completed. 

• Develop and maintain a program schedule including ensuring durations and accountabilities for all revenue generating milestones are accurate through the scope of the program (contract signature, PD US/DS, AD, Tech Transfer, Clinical-Commercial Manufacturing, QA, QC, Release, Ship Deliverables, Transfer in and Transfer out). 

• Collaborate with the Commercial Team to identify additional opportunities for additional work within the current contract. 

• Partner with functional teams (QC, QA, PD, Manufacturing, etc.) to ensure that program revenue generating milestones are accurately translated into functional deliverables and all action items are completed per the committed timeline. 

• Work closely with Process Development, Operations, Engineering, Quality Control and Quality Assurance to reduce time to clinic or market, improve ease of manufacturing, and reduce costs when compared with existing platform products while achieving and maintaining full compliance (cGMP, Safety and Environmental). 

• Accurately define timelines and resource requirements for the assigned programs. 

• Maintain program documentation (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 (financial, delivery metrics and analysis, monthly reports, quarterly and annual leadership reviews, revenue change log.   Ensure accurate and timely completion of financial transactions (revenue adjustments/ recognition, change orders, invoicing, pass through) and maintain a change log capturing all financial activity per program. 

• Responsible for authoring Scopes of Work, Change Orders, Cost Models, and Confidentiality Agreements.  

• 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 FLBT maintains best practices in the industry. 

• Expected to lead multiple programs in parallel in service of large, multi-program clients as well as manage one to two individual employees as part of role responsibilities.  

Required Skills & Abilities: 

• Excellent attention to detail with strong organizational and analytical skills. 

• Computer proficiency required, including strong experience with Microsoft Office (Word, Excel, PowerPoint) as well as Smartsheet.  

• 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. 

• Demonstrated effective resource and program planning/decision making. 

• 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. 

Working Conditions & 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 accommodation may be made to enable individuals with disabilities to perform the essential functions.  While performing the duties of this job, the employee is regularly required to: 

• 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. 

Qualifications: 

• Bachelor’s Degree preferably in Business, Engineering, Microbiology, Chemistry, Biochemistry, or related field; and   

• 10 years’ relevant project management experience. 

• 5 years of people leadership experience.  

Preferred Qualifications: 

• Relevant project management experience in biotechnology or pharmaceutical development and manufacturing environment managing one or more projects of medium to high complexity. 

• Certifications in Project/Risk Management or Lean Six Sigma  

• MBA or Master’s degree  

• Experience in a cGMP facility or working with FDA regulations. 

• Previous Accounting/Finance/Budgeting experience. 

To all agencies: Please, no phone calls or emails to any employee of FUJIFILM about this requisition. All resumes submitted by search firms/employment agencies to any employee at FUJIFILM via-email, the internet or in any form and/or method will be deemed the sole property of FUJIFILM, unless such search firms/employment agencies were engaged by FUJIFILM for this requisition and a valid agreement with FUJIFILM is in place. In the event a candidate who was submitted outside of the FUJIFILM agency engagement process is hired, no fee or payment of any kind will be paid.

Fujifilm is committed to providing equal opportunities in hiring, promotion and advancement, compensation, benefits, and training regardless of nationality, age, gender, sexual orientation or gender identity, race, ethnicity, religion, political creed, ideology, national, or social origin, disability, veteran status, etc.

If you require reasonable accommodation in completing this application, interviewing, completing any pre-employment testing, or otherwise participating in the employee selection process, please direct your inquiries to our HR Department (FDBTHR@fujifilm.com or (979) 431-3500).