Fujifilm-posted 13 days ago
Full-time • Entry Level
Onsite • Holly Springs, NC
501-1,000 employees

The QC Analyst is responsible for the key operational aspects of the QC Microbiology laboratory. Incumbent will perform microbial testing of all in -process drug substance, drug product, EM/UM, and raw materials samples. Incumbent will be responsible for all associated activities associated with this testing in accordance with written procedures. This position primarily works under minimal supervision as needed. This position will initially be involved in the commissioning activities involved in the construction of a new Biopharmaceutical manufacturing facility and laboratory. Flexibility in job roles and assignments will be required. This may include writing or assisting with document preparation and review, managing project timelines, conducting qualification and validation protocols, and assisting management with training and on-boarding of new staff as needed and in addition to regular work duties and assignments.

  • Collects samples for Environmental monitoring (EM) and Utilities monitoring (UM). Responsible for all sample collection and logistics as needed.
  • Coordinates testing materials and supplies needed for testing
  • Performs Basic Microbiology laboratory testing following standard procedures for all samples, including but not limited to all in-process samples, raw materials, EM and utilities samples for Bioburden, Endotoxin, plate reading, and microbial identification
  • Performs sterility testing, isolator qualification and routine operations and maintenance
  • Sample and data entry into LIMS system
  • Reviews general lab testing results
  • Troubleshoots routine assays
  • General laboratory support and laboratory maintenance in a cGMP laboratory including maintaining laboratory supplies needed for operations, maintenance of analytical instruments, purchasing and receiving of laboratory supplies (media, kits, etc.)
  • Ensures CAPAs are being followed in the laboratory areas
  • Notifies management and assists with the initiation of events (such as deviations) in the quality systems
  • Assists with projects as assigned
  • Works 12-hour shift on 2-2-3 cadence, 0600-1800
  • Performs other duties as assigned
  • BA/BS in scientific discipline
  • 0-2 years of basic GLP laboratory experience
  • Understanding of GMP, GLP, GDP requirements
  • Knowledgeable in basic sciences and Microbiology laboratory methods and procedures
  • Basic LIMS training
  • BS within Microbiology, Chemistry, Biochemistry, Biology
  • 2+ years of Intermediate experience in a GMP QC Microbiology Laboratory, knowledge of all compendial test methods (Bioburden, Endotoxin, sterility testing) preferred
  • Ability to troubleshoot and maintain laboratory equipment and instrumentation
  • Experience with microbial ID systems (MALDI, MicroSeq)
  • Intermediate LIMS training
  • Knowledge or training of FDA regulations (cGMP, cGLP, cGDP)
  • Trackwise System training
  • Lean / 6S training
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