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FUJIFILM DIOSYNTH BIOTECHNOLOGIES Quality Control Analyst (QC Analyst) II Microbiology in College Station, Texas

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QC Analyst II, Microbiology

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Job LocationsUS-TX-College Station

Posted Date

1 week ago

(12/26/2024 12:31 PM)

Requisition ID : 2024-32452

Category : Quality Control

Company (Portal Searching) : FUJIFILM Diosynth Biotechnologies

Overview

The work we do at FDB has never been more importantand we are looking for talented candidates to join us. We are growing our locations, our capabilities, and our teams, and looking for passionate, mission-driven people like you who want to make a real difference in peoples lives. Join FDB and help create the next vaccine, cure, or gene therapy in partnership with some of the most innovative biopharma companies across the globe. We are proud to cultivate a culture that will fuel your passion, energy and drive - what FDB call Genki.

External US

The Microbiologist II will be responsible for the QC microbiological aspects of cGMP compliance and testing at the FUJIFILM Biotechnologies Diosynth Texas (FDBT) Quality Control Laboratory.

Reports to

Supervisor, Microbiology

Work Location

College Station, TX

Primary Responsibilities:

  • Performs QC microbiological aspects of cGMP compliance and testing.
  • Collect environmental monitoring (Total Air, Viable Air and Viable Surface) in a cleanroom/controlled environment.
  • Collect Utility Monitoring Samples (RODI/WFI) routinely and for qualification of systems.
  • Perform incubation/enumeration of environmental samples.
  • Gram stain/Characterization of environmental isolates.
  • Performs testing for water samples (pH/Conductivity, TOC, Water Bioburden, Endotoxin).
  • Ensure lab is maintained (organized, clean, and properly supplied).
  • Perform other duties as assigned.

Qualifications:

Bachelors degree preferably in

Biochemistry, Chemistry, Biology, or related field with 1+ year of relevant GMP experience; OR

Associates degree preferably in

Biochemistry, Chemistry, Biology, or related field with 2+ years of relevant GMP experience; OR

High School Diploma or GED

with 3+ years of relevant GMP experience.

Sound aseptic technique and understanding of industry best practices, techniques, equipment, and materials.

Ability to analyze raw data, assess assay and system suitability criteria.

Ability to follow safety procedures outlined in the Chemical Hygiene Plan.

Utilize SDS sheets to properly assess chemical hazards, spill response procedures, and PPE requirements if indicated.

Good attention to detail and ability to utilize problem solving/trouble shooting skills.

Good computer skills.

Demonstrated written and oral communication skills.

Demonstrated leadership skills.

Strong organization and analytical skills.

Role

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