Fujifilm-posted 1 day ago
Full-time • Mid Level
Onsite • Research Triangle Park, NC
501-1,000 employees

Position Overview The Production Technician 4 leads and executes manufacturing processing steps and associated activities while maintaining strict adherence to Current Good Manufacturing Practice (CGMP), quality and regulatory standards. Flexibility with working hours and shift rotation is essential to effectively support the 24/7 manufacturing facility. Company Overview At FUJIFILM Biotechnologies, we’re leading the charge in advancing tomorrow’s medicines. If you want to be a part of life-impacting projects alongside today’s most innovative biopharmaceutical companies, FUJIFILM Biotechnologies could be the right place for you. From our Bioprocess Innovation Center to our cGMP-compliant manufacturing site, we thrive on collaboration, creativity, and purpose. Whether your expertise lies in research, manufacturing, or production, you’ll find a home here where your efforts directly improve patients’ lives. Together, let’s shape the future of healthcare. Situated at the cross-section of Morrisville and Research Triangle Park (RTP), North Carolina, our site is at the heart of a booming biotech hub surrounded by top universities, vibrant communities, and various outdoor opportunities. 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 Job Description

  • Executes, documents, and leads manufacturing processing steps or support activities, process monitoring and control within at least one functional area (e.g., Fermentation, Purification, Recovery, Cell Culture) and one additional core responsibility (e.g., Filtration, Homogenization/ Centrifugation, Fermentation, Chromatography, Cell Culture)
  • Performs in-process testing (e.g., pH, conductivity, visual inspection)
  • Executes validation protocols according to Current Good Manufacturing Practice (CGMP) standard operating procedures (SOPs)
  • Leads the manufacturing suite and manages materials for the assigned manufacturing functional area, as needed
  • Performs manufacturing task execution using all area applicable Distributed Control System (DCS), DeltaV, 800xA, Unicorn, etc.
  • Closes Shop Floor Orders (SFOs) in the Manufacturing Execution System (MES) in a timely manner
  • Serves as the subject matter expert (SME) in at least one of the core responsibilities within the manufacturing assigned area
  • Leads tier 1 discussions, as needed
  • Assists senior level associates or supervisor with scheduling daily activities on the manufacturing floor, as needed
  • Maintains training to perform all required activities
  • Performs other duties, as assigned
  • Effective communication, both written and verbal
  • Strong knowledge of CGMP and safety regulations, and pharmaceutical industry standards
  • Proficient understanding of manufacturing run cadence and order of shift activities
  • Ability to work in a team environment and willingness to train or mentor others
  • Strong time management and troubleshooting skills
  • Ability to initiate a deviation and progress to impact assessment in designated functional area
  • Ability to initiate a work order in the Computerized Maintenance Management System (CMMS)
  • Must be able to support 24/7 manufacturing facility working shift (2-2-3 day/night)
  • High School Diploma/GED with 6+ years of experience in a CGMP manufacturing environment; or Associate degree in life science, engineering, or relevant technical field with 4+ years of experience in a CGMP manufacturing environment; or Bachelor’s degree in life science, engineering, or relevant technical field with 2+ years of experience in a CGMP manufacturing environment; or Equivalent Military training or experience
  • Experience with unit operation (e.g., Cell Culture, Fermentation, etc.)
  • BioWork certificate
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