QC Job at FUJIFILM Biotechnologies, USA | Life Science | Apply Now
If you are an early-career biology graduate or an experienced laboratory technician looking to anchor your career within a world-class biologics manufacturing network, this full-time role at FUJIFILM Diosynth Biotechnologies is an exceptional opportunity. Located at our advanced facility in the booming biotech hub of the Research Triangle Park (RTP) region in North Carolina, this position places you on the frontline of contamination control and aseptic safety validation. For quality-driven specialists searching for a high-value QC Job, this position offers hands-on mastery over clean utility collection, Environmental Monitoring (EM) protocols, and Laboratory Information Management Systems (LIMS). It serves as an elite operational launchpad for a long-term FUJIFILM Biotechnologies career and stands out as a premier choices for anyone tracking a competitive, compliance-driven Life Sciences Job within the commercial biopharmaceutical sector.
- Job Position: QC Associate I
- Location: Triangle, NC
About The Company
FUJIFILM Diosynth Biotechnologies is a world-leading Contract Development and Manufacturing Organization (CDMO) dedicated to helping today’s most innovative biopharmaceutical partners discover, develop, and manufacture tomorrow’s medicines. Spanning foundational science to commercial-scale cGMP production, the organization operates advanced facilities across the globe, supporting therapies that directly improve patient outcomes. The advanced bioprocess campus, situated at the cross-section of Morrisville and Research Triangle Park, North Carolina, functions as a high-throughput hub for mammalian cell cultures and viral vectors. Joining this Quality Control Microbiology unit inserts you into a purpose-driven environment where your efforts safeguard the drug supply pipeline, ensuring that every batch complies with global regulatory standards.
QC Job – Key Responsibilities
The QC Associate I assumes daily operational responsibility for executing environmental monitoring plans, testing clean utilities, and protecting data integrity across production areas.
Your core experimental, instrumentation tracking, and quality control duties include:
- Environmental Monitoring (EM): Performing routine EM sampling inside classified cGMP cleanrooms and production spaces to ensure strict microbial control.
- Clean Utilities Testing: Conducting the collection and rigorous testing of critical site utilities, including high-purity water systems, clean steam, and compressed gases.
- Data Log Entry: Entering real-time laboratory metrics, assay readouts, and sampling data into the Laboratory Information Management System (LIMS) to advance this QC Job.
- Quality Systems Support: Assisting area management with technical services, including identifying anomalies and initiating event notifications (such as deviations and non-conformances) via specialized tracking systems.
- Inspection Readiness & CGMP: Ensuring the microbiology laboratory maintains constant data integrity, strict audit readiness, and complete compliance with Current Good Manufacturing Practices (cGMP).
- Equipment Qualification: Partnering with laboratory management to schedule daily testing tasks and leading or participating in routine laboratory instrument qualifications and validations.
Qualifications & Profile Requirements For QC Job
This role is systematically structured with flexible onboarding pathways, welcoming entry-level university graduates alongside experienced vocational analysts.
- Education & Experience Pathways (Must meet one of the following):
- Pathway 1: A Bachelor’s degree in Life Science or Biology with no prior experience in a cGMP environment to launch a FUJIFILM Biotechnologies career.
- Pathway 2: An Associate’s degree in a Life Science, or related field paired with at least 2 years of laboratory experience in a cGMP environment.
- Pathway 3: A High School Diploma paired with at least 4 years of hands-on laboratory experience in a regulated cGMP environment.
- Core Knowledge, Skills & Abilities:
- Strong working knowledge of aseptic techniques, microbial control behaviors, and the physical capability to aseptically gown into classified manufacturing cleanrooms.
- Familiarity with international compendia standards, including the United States Pharmacopeia (USP) and European Pharmacopeia (EP).
- Expertise with data management platforms (such as TrackWise or LIMS) and a willingness to incorporate lean lab and Six Sigma principles into a premium Life Sciences Job track.
- Technical writing capabilities, effective verbal communication, and independent problem-solving skills.
- High flexibility to support a 24/7 manufacturing facility, including overtime or temporary shift updates to satisfy testing parameters with short analytical windows (e.g., 12-hour bioburden tests).
- Preferred Asset: Possession of an active BioWork Certificate is a distinct corporate plus.
In short, the QC Associate I position at FUJIFILM Diosynth Biotechnologies is a definitive route to transitioning your life sciences background into a premier biomanufacturing asset. Securing this appointment allows you to step past generalized entry-level tasks and take direct operational charge of the cleanroom samplings, utility validations, and deviation tracking workflows that secure global therapeutic supply chains. If you reside in North Carolina, meet the educational parameters, and possess an compromise-free approach to cGMP data integrity, apply today to secure this premier QC Job, launch a highly rewarding FUJIFILM Biotechnologies career, and lock in this outstanding Life Sciences Job.
