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Job description
Manufacturing Associate 3, Drug ProductHelp deliver safe, high-quality medicines at scale. As a Manufacturing Associate 3, Drug Product, you'll play a hands-on role in component/parts preparation, thawing and formulation, sterile filling, and visual inspection—supporting a 24/7 operation that keeps patients at the center.Fujifilm Biotechnologies is building the future of bioproduction in Holly Springs, North Carolina. By end of 2025, we'll open North America's largest end-to-end CDMO biopharmaceutical manufacturing facility, offering drug substance production, fill-finish, and packaging under one roof.We're 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 we're proud to cultivate a culture that will fuel your purpose, energy, and drive—what we call Genki. Ready to shape the future of medicine? Let's transform healthcare together!Holly Springs, North Carolina, combines small-town warmth with proximity to Raleigh's 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."Job DescriptionAbout UsWe are a collaborative Drug Product manufacturing team committed to operational excellence, safety, and cGMP compliance.You'll help shape processes, train new colleagues, and support equipment qualification and startup activities for our DPFG facility.Our environment values clear communication, teamwork, and continuous improvement—so you can contribute, learn, and grow.Minimum qualifications (one of the following is required):High School Diploma or GED with 4+ years of direct experience in a cGMP manufacturing environment; ORAssociate's Degree with 2 years of direct experience in a cGMP manufacturing environment; ORBachelor's Degree (preferably Life Sciences or Engineering); OREquivalent military training or experiencePreferred qualifications:Qualified experience on unit operations such as Parts Washer, Autoclave Operation, Compounding/Formulation, Filling with Isolator Technology, or Manual/Automated Visual InspectionBioWorks or BTEC Capstone cGMP courseworkWhat helps you succeed:Ability to assist in troubleshooting and apply sound judgment on assignmentsStrong verbal and written communication skillsKnowledge of production equipment operations within your unit operation(s)Basic understanding of manufacturing run cadence and order of shift activitiesKnowledge of cGMP, safety, and operational proceduresAbility to work effectively in a team environmentFlexibility for shift rotation and weekend/night work in a 24/7 facilityResponsibilitiesLead, execute, and document manufacturing processing steps and/or support activities, including process monitoring and controlPerform in-process testing (e.g., pH, conductivity, visual inspection) with accuracy and attention to detailExecute validation protocols in alignment with cGMP Standard Operating Procedures (SOPs)Maintain training qualifications to perform all required manufacturing activitiesPerform operations across Drug Product unit operations, including:Parts Washer and AutoclaveCompounding/FormulationSterile Filling (including isolator technology)Manual and/or Automated Visual InspectionAssist and/or lead cycle counts; manage materials for assigned manufacturing areasAssist the lead with daily manufacturing tasks and coordinate daily shift activities as neededSupport projects that improve Drug Product manufacturing processes, including training of new colleaguesMaintain compliance of cGMP documents and assist in equipment qualification and DPFG facility startup activitiesFollow safe work practices and escalate issues promptly to maintain product quality and complianceThis role may require shift work (weekends and potential nights) and other duties as assignedBenefitsCompetitive pay with shift differentials where applicableComprehensive health coverage (medical, dental, vision)Paid time off, holidays, and sick leaveRetirement savings plan with company contributionTraining and development opportunities, including cGMP upskilling and mentorshipInclusive, team-centered culture focused on safety, quality, and continuous improvementEmployee assistance and well-being resourcesOpportunities to contribute to startup and optimization initiatives in a modern DP facilityWork environment and physical requirements (role-specific)May require respiratory and hearing protection; ability to discern audible cues and perform tasks requiring 20/20 corrected vision (including color)Ability to ascend/descend ladders; perform repetitive motions with wrists/hands/fingersAbility to operate machinery/power tools and, as required, motor vehicles or Powered Industrial TrucksAbility to lift/move up to 33 lbs; bend, push/pull, and reach between 18" and 60" in heightComfortable working at heights greater than 4 feetProlonged standing and sitting may be required depending on shift activitiesEEO InformationFujifilm 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.ADA InformationIf 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 ( ).
Worksite address
holly springs, NC, 27540, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.