Senior Engineer/Scientist 2, Process Analytics

The Senior Engineer or Scientist 2 of Process Analytics serves as the subject matter expert (SME) and provides technology transfer support, technical oversight, and strategic input for Process Analytical Technologies (PAT). This role will lead PAT deployment, integration, and modeling activities while interfacing with clients and internal teams to ensure successful technology delivery, routine use, and continuous improvement.

FUJIFILM Biotechnologies is building the future of bioproduction in Holly Springs, North Carolina. By end of 2025, well open North Americas largest end-to-end CDMO biopharmaceutical manufacturing facility, offering drug substance production, fill-finish, and packaging under one roof.

Were looking for passionate, mission-driven people to help us realize this exciting vision and deliver the next vaccine, cure, or therapy. We offer a dynamic work environment and were proud to cultivate a culture that will fuel your purpose, energy, and drivewhat we call Genki. Ready to shape the future of medicine? Lets transform healthcare together!

Holly Springs, North Carolina, combines small-town warmth with proximity to Raleighs thriving tech scene, making it the perfect blend of community and opportunity.

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:

What Youll Do

Provides oversight on all aspects of site readiness, technology transfer (TT) programs, and ongoing manufacturing activities related to process analytics (PA) deliverablesEstablishes and ensures timelines and plans align with relevant stakeholders and that deliverables are successfully completed on timeEnsures team project plans are integrated with other scheduling functions within the organization and in alignment with program scopeEscalates risks and tracks milestone progress while ensuring cross functional communication to key stakeholdersProvides oversight on the execution and advancement of process trends and process verification plansServes as the point of contact to customer and internal regulatory team for technical aspects of the process and programFacilitates delivery of documentation for internal and external use, such as comprehensive written manufacturing protocols and reports summarizing investigations, studies, and projectsServes as the subject matter expert (SME) while leading and conducting troubleshooting, process impact assessments, and executing root cause analysis (RCA) and corrective and preventive action (CAPA) in response to deviationsManages Chemistry, Manufacturing and Control (CMC) activities for development and manufacturing, including coordination and input to customer regulatory filingsIdentifies training needs and facilitates training for laboratory and manufacturing teamsOversees the development and roll-out of training content related to PA toolsSupports role in Good Manufacturing Practices (GMP) environmentLeads the technical team with investigating project challenges through risk assessment tools and techniques, as neededCloses deviations and provides a thorough explanation of findings to internal and external stakeholdersUtilizes new knowledge to promptly drive data-based decisionsEnsures master batch records (MBRs) and sample plans support PA requirementsNegotiates with cross-functional stakeholdersOversees data stewardship and data governance activities, including alignment with global FDB networkEnsures data and analyses are findable, accessible, interoperable, and reusable to internal and external stakeholdersLeads best practices for TT and process performance qualification (PPQ) strategies globally, as requiredOversees informatics and data systems improvement initiatives to improve scalability, manufacturability, reliability, yield and costServes as a key contributor to the PA strategic roadmap development and owns delivery of assigned itemsCommunicates and aligns roadmap elements with internal and external stakeholders, as directedOversees the evaluation of new analytical technologies (e.g., Process Analytical Technologies (PAT), Data Science tools) and the development of new solutionsProvides guidance on implementation and sustainment strategiesOversees stewardship of critical knowledge for PA tools, PAT, and supporting systemsWrites, reviews, and provides SME feedback for standard operating procedures (SOPs), work instructions, white papers, and other relevant documentationRoutinely represents FDB at technical conferences, seminars, etc. and engages the biotechnology communityRemains up to date on best practices and industry trends and ensures PA team is awareDevelops presentations, publications, scientific articles, and other materials for external engagement with the external scientific communityFacilitates the design of study and/or sampling protocols by ensuring the PA and Manufacturing teams provide input and reviewMentors junior team members, lab, and manufacturing colleaguesOther duties, as assigned

Knowledge and Skills

Ability to adapt communication style to differing audiences and advise others on difficult mattersAdvanced problem-solving and project management skillsAbility to effectively present complex information to othersAbility to develop effective working relationships internally and externallyProficient with Snowflake and PythonProficient with structured query language (SQL) writing skillsStrong knowledge of process historians and data management systems (e.g., OSI PI, Statistica, SIMCA)Proficient knowledge in Statistical Process Control (SPC) and multivariate data analysis

Strong knowledge of machine learning techniques, data science, and PATProficient knowledge of regulatory requirements related to data integrity and PATIntermediate knowledge of business acumen, negotiation tactics, and ability to build business casesProficient ability to integrate and facilitate activities across multiple teamsAbility to remain up to date on best practices and industry trends

Basic Requirements

Bachelors degree in Data Science, Biotechnology, or Chemical Engineering with 12 years of relevant experience (e.g., data engineering, manufacturing, bioprocess development, PAT); orMasters degree with 8 years of relevant experience (e.g., data engineering, manufacturing, bioprocess development, PAT); orPhD with 5 years of relevant experience (e.g., data engineering, manufacturing, bioprocess development, PAT)Experience working in a GMP environmentExperience using Quality Systems (e.g., Deviation Management system, Change Control, CAPA, document management system)Experience using Risk Management and RCA toolsExperience with multivariate modeling and/or PAT applicationPrior experience leading new technology or method implementations and sustainment projects

Preferred Requirements

Prior biologics drug substance and manufacturing experience, including process development, validation, and transferExperience authoring CMC sections for regulatory filings and supporting regulatory auditsExperience transferring and scaling new technologies and/or methods across a manufacturing networkExperience working with a wide range of data analytics architectures (e.g., warehousing, distributed computing, visualization analytics)Experience leading and influencing cross-functional teams

WORKING CONDITIONS & PHYSICAL REQUIREMENTS

Will work in environment which may necessitate respiratory protection X No YesMay work in Mechanical/Production spaces that may require hearing protection and enrollment in a hearing conservation program. X No YesWill work in environment operating a motor vehicle or Powered Industrial Truck. X No YesAbility to discern audible cues. No X YesAbility to inspect or perform a task with 20/20 corrected vision, visual acuity, including distinguishing color. X No Yes

Ability to ascend or descend ladders, scaffolding, ramps, etc. X No YesAbility to stand for prolonged periods of time. X No YesAbility to sit for prolonged periods of time. X No YesAbility to conduct activities using repetitive motions that include writs, hands and/or fingers. X No YesAbility to operate machinery and/or power tools. X No YesAbility to conduct work that includes moving objects up to X pounds. X No Yes If yes, 10 lbs. 33 lbs.Ability to bend, push or pull, reach to retrieve materials from 18 to 60 in height, and use twisting motions. X No Yes

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 (...).