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Lead QC Associate III - Microbiology

Job in Cary, Wake County, North Carolina, 27518, USA
Listing for: FUJIFILM Holdings America Corporation
Full Time position
Listed on 2026-08-26
Job specializations:
  • Quality Assurance - QA/QC
  • Healthcare
    Data Scientist, Medical Science
Salary/Wage Range or Industry Benchmark: 90000 - 130000 USD Yearly USD 90000.00 130000.00 YEAR
Job Description & How to Apply Below

Position Overview

The Lead Associate 3, Quality Control (QC) Microbiology oversees and guides the critical operational functions of the QC Microbiology laboratory. This position holds the responsibility for conducting microbiological assays, as well as effectively trains junior analysts in these areas. The role is pivotal in guaranteeing “right the first time” execution to support timely batch disposition of manufacturing goods. Additionally, this role ensures technical issues are promptly escalated to laboratory management and upholds high standards of accuracy and efficiency within the laboratory operations.

Shift: Monday – Friday (8am – 5pm)

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:

Job Description

What You’ll Do:

  • Performs complex microbiological testing (e.g., Bioburden, Endotoxin, Culture Purity, and Microbial Identifications) per department Standard Operating Procedures (SOPs) and test methods for samples associated manufactured batches
  • Reviews technical data, authors routine and periodic laboratory reports (e.g., Environmental Monitoring (EM) trend reports) and contributes to technical documentation and assessments
  • Supports client audits and regulatory inspections as an assay or method Subject Matter Expert (SME)
  • Ensures laboratory maintains inspection readiness, data integrity, and Current Good Manufacturing Practice (CGMP) compliance
  • Partners with management for technical services, such as initiating events (e.g., deviations and non-conformances) within quality systems
  • Leads laboratory deviations and investigations
  • Identifies problems, recommends and implements solutions while consulting with management
  • Leads and participates in project developments from concept through execution, ensuring alignment with organizational goals
  • Partners with laboratory management to schedule daily, weekly, and non-routine testing and tasks
  • Provides technical guidance and mentorship to junior associates
  • Participates in laboratory equipment qualification and validation activities
  • Troubleshoots laboratory equipment, assay and method issues with the support of laboratory management

Knowledge, Skills, or Abilities
:

  • Advanced knowledge of aseptic techniques and behaviors
  • Effective communication, both written and verbal
  • Advanced technical writing and problem-solving skills
  • Ability to complete work independently and with minimal supervision
  • Ability to prioritize and organize work to deliver assignments according to established schedules and deadlines
  • Ability to effectively collaborate with coworkers and internal clients
  • In-depth understanding and knowledge of United States Pharmacopeia and European Pharmacopeia
  • Ability to support audit readiness for the laboratory
  • Ability to incorporate lean lab and six sigma principles into the work environment
  • Ability to manage and complete tasks according to a structured plan
  • Expertise with data management systems, such as Track Wise, LIMS, and capability to learn basic use and navigation within the systems
  • Must be flexible to support 24/7 manufacturing facility

Minimum Requirements
:

  • Bachelor’s degree in Life Science, Pharmaceutical, or related field with 4+ years of…
Position Requirements
10+ Years work experience
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