bluedoor data·Job Postings API·bluedoor.sh ↗

HomeCompaniesUscareershub Fujifilm Icims ComQC Associate I, Environmental Monitoring

QC Associate I, Environmental Monitoring

Uscareershub Fujifilm Icims Com · Research Triangle Park, NC, US · On Site · Active · iCIMS

Job facts

FieldValue
CompanyUscareershub Fujifilm Icims Com
TitleQC Associate I, Environmental Monitoring
Normalized title-
Department / teamQuality Control
LocationResearch Triangle Park, NC, United States
Work modelOn Site
Employment typeOTHER
Salary-
Statusactive
ATS provideriCIMS
Posted / first seen2026-03-30 / 2026-05-31
Changed / last seen2026-06-01 / 2026-06-23

Related slices

PageWhat it containsOpen
Company jobsActive postings from Uscareershub Fujifilm Icims Com.Open
Company breakdownsRole, location, ATS, and work model facets for this company.Open
ATS provider jobsActive postings observed through iCIMS.Open
Provider filtered searchThe same provider as a filtered job collection.Open
City jobsActive postings in Research Triangle Park.Open
Department jobsActive postings in Quality Control.Open
Work model jobsActive On Site postings.Open
Lifecycle eventsOpen, update, close, and reopen events for this posting.Open
Original postingCanonical source or apply URL captured from the ATS.Open

Linked records

CompanyUscareershub Fujifilm Icims Com
Source6a86663d-e7d5-4a9b-a4c9-cc12544fb1a3
ATS provideriCIMS

Description

Position Overview The QC Associate I role in Quality Control Microbiology is crucial for performing operational functions of the QC Microbiology laboratory. This position holds the responsibility for conducting environmental and clean utility monitoring and standard microbiological assays. The incumbent will operate under guidance of laboratory supervisors and lead analysts, ensuring technical issues are promptly escalated to laboratory management. Tasks will be assigned to off-shift personnel where possible. Overtime and temporary shift changes will be required to support programs that have samples with short testing windows (e.g., bioburden 12-hours). 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 Major Accountabilities : Supports manufacturing operations through routine EM of classified production areas Provides facility support through the collection and testing of site clean utilities (e.g., water, steam, and compressed gases) Enters data into the Laboratory Information Management System (LIMS) Ensures laboratory maintains inspection readiness, data integrity, and Current Good Manufacturing Practice (CGMP) compliance. Assists management with technical services, such as initiating events (e.g., deviations and non-conformances) within quality systems. Identifies and solves problems while informing and consulting with area management. Partners with laboratory management in scheduling of daily, weekly, and non-routine testing and tasks. Participate or lead laboratory equipment qualification or validation. Performs other duties, as assigned. Knowledge, Skills or Abilities: Strong working knowledge of aseptic techniques and behaviors Effective communication, both written and verbal Technical writing and problem-solving skills Ability to aseptically gown into classified manufacturing spaces Ability to complete work both independently 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 Ability to support audit readiness for the laboratory Familiarity with United States Pharmacopeia and European Pharmacopeia Willingness to learn and 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 TrackWise, LIMS, and capability to learn basic use and navigation within the systems Must be flexible to support 24/7 manufacturing facility Minimum Education Requirements High School Diploma and at least 4 years of laboratory experience in a cGMP environment; or Associate’s degree in Life Science, Pharmaceutical, or related field with at least 2 years of laboratory experience in a cGMP environment; or Bachelor’s degree in Life Science or Biology with no prior experience in a cGMP environment Preferred Experience BioWork Certificate Physical Requirements: Will work in environment which may necessitate repiratory protection Ability to discern audible cues Ability to inspect or perform a task with 20/20 corrected visition, visual acuity, including distinguishing color Ability to asend or descend ladders, scaffolding, ramps, etc. Ability to stand for prolonged periods of time (240 minutes) Ability to sit for prolonged periods of time (240 minutes) Ablity to conduct activities using repetitive motions that include wrists, hands, and/or fingers Ability to conduct work that includes moving objects up to 33lbs Ability to bend, push or pull, reach to retrieve materials from 18" to 60" in height, and use twisting motions. Will work in warm/cold environments (0-100F range) *#LI-Onsite To all agencies: Please, no phone calls or emails to any employee of FUJIFILM about this requisition. All resumes submitted by search firms/employment agencies to any employee at FUJIFILM via-email, the internet or in any form and/or method will be deemed the sole property of FUJIFILM, unless such search firms/employment agencies were engaged by FUJIFILM for this requisition and a valid agreement with FUJIFILM is in place. In the event a candidate who was submitted outside of the FUJIFILM agency engagement process is hired, no fee or payment of any kind will be paid. EEO Information Fujifilm is committed to providing equal opportunities in hiring, promotion and advancement, compensation, benefits, and training regardless of nationality, age, gender, sexual orientation or gender identity, race, ethnicity, religion, political creed, ideology, national, or social origin, disability, veteran status, etc. ADA Information If you require reasonable accommodation in completing this application, interviewing, completing any pre-employment testing, or otherwise participating in the employee selection process, please direct your inquiries to our HR Department ([email protected]).

Full job record

Job ID8dd0d0b03102a3dfefd8bbb8f1d1d319b2a025e4
Org ID63e98acc-2d53-4b16-a0e9-913c8cd24452
Source ID6a86663d-e7d5-4a9b-a4c9-cc12544fb1a3
Board ID6a86663d-e7d5-4a9b-a4c9-cc12544fb1a3
Providericims
Provider Job Key37362
TitleQC Associate I, Environmental Monitoring
Normalized Title
Statusactive
Activeyes
Location TextResearch Triangle Park, NC, US
DepartmentQuality Control
Team
Employment TypeOTHER
Workplace Typeon_site
Remote Policy
CountryUnited States
RegionNC
CityResearch Triangle Park
Salary RawPosition Overview The QC Associate I role in Quality Control Microbiology is crucial for performing operational functions of the QC Microbiology laboratory. This position holds the responsibility for conducting environmental and clean utility monitoring and standard microbiological assays. The incumbent will operate under guidance of laboratory supervisors and lead analysts, ensuring technical issues are promptly escalated to laboratory management. Tasks will be assigned to off-shift personnel where possible. Overtime and temporary shift changes will be required to support programs that have samples with short testing windows (e.g., bioburden 12-hours). 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 Major Accountabilities : Supports manufacturing operations through routine EM of classified production areas Provides facility support through the collection and testing of site clean utilities (e.g., water, steam, and compressed gases) Enters data into the Laboratory Information Management System (LIMS) Ensures laboratory maintains inspection readiness, data integrity, and Current Good Manufacturing Practice (CGMP) compliance. Assists management with technical services, such as initiating events (e.g., deviations and non-conformances) within quality systems. Identifies and solves problems while informing and consulting with area management. Partners with laboratory management in scheduling of daily, weekly, and non-routine testing and tasks. Participate or lead laboratory equipment qualification or validation. Performs other duties, as assigned. Knowledge, Skills or Abilities: Strong working knowledge of aseptic techniques and behaviors Effective communication, both written and verbal Technical writing and problem-solving skills Ability to aseptically gown into classified manufacturing spaces Ability to complete work both independently 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 Ability to support audit readiness for the laboratory Familiarity with United States Pharmacopeia and European Pharmacopeia Willingness to learn and 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 TrackWise, LIMS, and capability to learn basic use and navigation within the systems Must be flexible to support 24/7 manufacturing facility Minimum Education Requirements High School Diploma and at least 4 years of laboratory experience in a cGMP environment; or Associate’s degree in Life Science, Pharmaceutical, or related field with at least 2 years of laboratory experience in a cGMP environment; or Bachelor’s degree in Life Science or Biology with no prior experience in a cGMP environment Preferred Experience BioWork Certificate Physical Requirements: Will work in environment which may necessitate repiratory protection Ability to discern audible cues Ability to inspect or perform a task with 20/20 corrected visition, visual acuity, including distinguishing color Ability to asend or descend ladders, scaffolding, ramps, etc. Ability to stand for prolonged periods of time (240 minutes) Ability to sit for prolonged periods of time (240 minutes) Ablity to conduct activities using repetitive motions that include wrists, hands, and/or fingers Ability to conduct work that includes moving objects up to 33lbs Ability to bend, push or pull, reach to retrieve materials from 18" to 60" in height, and use twisting motions. Will work in warm/cold environments (0-100F range) *#LI-Onsite To all agencies: Please, no phone calls or emails to any employee of FUJIFILM about this requisition. All resumes submitted by search firms/employment agencies to any employee at FUJIFILM via-email, the internet or in any form and/or method will be deemed the sole property of FUJIFILM, unless such search firms/employment agencies were engaged by FUJIFILM for this requisition and a valid agreement with FUJIFILM is in place. In the event a candidate who was submitted outside of the FUJIFILM agency engagement process is hired, no fee or payment of any kind will be paid. EEO Information Fujifilm is committed to providing equal opportunities in hiring, promotion and advancement, compensation, benefits, and training regardless of nationality, age, gender, sexual orientation or gender identity, race, ethnicity, religion, political creed, ideology, national, or social origin, disability, veteran status, etc. ADA Information If you require reasonable accommodation in completing this application, interviewing, completing any pre-employment testing, or otherwise participating in the employee selection process, please direct your inquiries to our HR Department ([email protected]).
Salary Min
Salary Max
Salary Currency
Salary Periodhour
Source URLhttps://uscareershub-fujifilm.icims.com/jobs/37362/qc-associate-i%2c-environmental-monitoring/job
Apply URLhttps://uscareershub-fujifilm.icims.com/jobs/37362/qc-associate-i%2c-environmental-monitoring/job
First Seen At2026-05-31 18:42:38Z
Last Seen At2026-06-23 08:31:38Z
Last Checked At2026-06-23 08:31:38Z
Last Changed At2026-06-01 13:48:04Z
Inactive At
Source Posted At2026-03-30 04:00:00Z
Source Updated At2026-04-07 18:58:36Z
Raw Payload Uris3://job-postings-prod-raw-590183727216/raw/provider=icims/board=uscareershub-fujifilm.icims.com/date=2026-06-23/2026-06-23T08-31-29-244Z-0b0e2d1c9632ed521534f8c9d3b7244f15550ad330e507cbfce261351253562e.json
Event Fields
{
  "content_hash": "bf1a32b65437454f757f7ffa05232e62ca564a81c4fa202b920080456ad6c3ef",
  "source_hash": "78363e16eb220c673834625c80c83e3f7cf82f8783095467dbc8f8da9cf4dd4c",
  "last_changed_at": "2026-06-01T13:48:04.333Z",
  "active_status": "active"
}
Parsed Structured
{
  "dedupe": null,
  "language": "en",
  "location": {
    "raw": "Research Triangle Park, NC, US",
    "city": "Research Triangle Park",
    "region": "NC",
    "country": "United States",
    "is_remote": false,
    "confidence": 0.8
  },
  "salary_max": null,
  "salary_min": null,
  "inferred_at": "2026-06-23T08:31:38.804Z",
  "launch_scope": {
    "reason": "english_us_canada",
    "included": true,
    "language": "en",
    "location": {
      "raw": "Research Triangle Park, NC, US",
      "city": "Research Triangle Park",
      "region": "NC",
      "country": "United States",
      "is_remote": false,
      "confidence": 0.8
    },
    "countries": [
      "United States"
    ]
  },
  "remote_policy": null,
  "salary_period": "hour",
  "workplace_type": "on_site",
  "salary_currency": null
}
Extensions
{}
Native Structured
{
  "json_ld": {
    "url": "https://uscareershub-fujifilm.icims.com/jobs/37362/qc-associate-i%2c-environmental-monitoring/job",
    "@type": "JobPosting",
    "title": "QC Associate I, Environmental Monitoring",
    "@context": "http://schema.org",
    "datePosted": "2026-03-30T04:00:00.000Z",
    "description": "<h2>Position Overview</h2>\n<p>The QC Associate I role in Quality Control Microbiology is crucial for performing operational functions of the QC Microbiology laboratory. This position holds the responsibility for conducting environmental and clean utility monitoring and standard microbiological assays. The incumbent will operate under guidance of laboratory supervisors and lead analysts, ensuring technical issues are promptly escalated to laboratory management. Tasks will be assigned to off-shift personnel where possible.  Overtime and temporary shift changes will be required to support programs that have samples with short testing windows (e.g., bioburden 12-hours).</p>\n<h2>Company Overview</h2>\n<p>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.</p> \n<p>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.</p> \n<p>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.</p> \n<p>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</p>\n<h2>Job Description</h2>\n<p><strong>Major Accountabilities</strong>: </p>\n<ul>\n <li>Supports manufacturing operations through routine EM of classified production areas</li>\n <li>Provides facility support through the collection and testing of site clean utilities (e.g., water, steam, and compressed gases)</li>\n <li>Enters data into the Laboratory Information Management System (LIMS)</li>\n <li>Ensures laboratory maintains inspection readiness, data integrity, and Current Good Manufacturing Practice (CGMP) compliance.</li>\n <li>Assists management with technical services, such as initiating events (e.g., deviations and non-conformances) within quality systems.</li>\n <li>Identifies and solves problems while informing and consulting with area management.</li>\n <li>Partners with laboratory management in scheduling of daily, weekly, and non-routine testing and tasks.</li>\n <li>Participate or lead laboratory equipment qualification or validation.</li>\n <li>Performs other duties, as assigned.</li>\n</ul>\n<p><strong>Knowledge, Skills or Abilities: </strong></p>\n<ul>\n <li>Strong working knowledge of aseptic techniques and behaviors </li>\n <li>Effective communication, both written and verbal</li>\n <li>Technical writing and problem-solving skills</li>\n <li>Ability to aseptically gown into classified manufacturing spaces</li>\n <li>Ability to complete work both independently with minimal supervision</li>\n <li>Ability to prioritize and organize work to deliver assignments according to established schedules and deadlines</li>\n <li>Ability to effectively collaborate with coworkers and internal clients</li>\n <li>Ability to support audit readiness for the laboratory</li>\n <li>Familiarity with United States Pharmacopeia and European Pharmacopeia</li>\n <li>Willingness to learn and incorporate lean lab and six sigma principles into the work environment</li>\n <li>Ability to manage and complete tasks according to a structured plan</li>\n <li>Expertise with data management systems, such as TrackWise, LIMS, and capability to learn basic use and navigation within the systems </li>\n <li>Must be flexible to support 24/7 manufacturing facility</li>\n</ul>\n<p> </p>\n<p><strong>Minimum Education Requirements</strong></p>\n<ul>\n <li>High School Diploma and at least 4 years of laboratory experience in a cGMP environment; or</li>\n <li>Associate’s degree in Life Science, Pharmaceutical, or related field with at least 2 years of laboratory experience in a cGMP environment; or </li>\n <li>Bachelor’s degree in Life Science or Biology with no prior experience in a cGMP environment</li>\n</ul>\n<p><strong>Preferred Experience</strong></p>\n<ul>\n <li>BioWork Certificate</li>\n</ul>\n<p><strong>Physical Requirements:</strong></p>\n<ul>\n <li>Will work in environment which may necessitate repiratory protection</li>\n <li>Ability to discern audible cues</li>\n <li>Ability to inspect or perform a task with 20/20 corrected visition, visual acuity, including distinguishing color</li>\n <li>Ability to asend or descend ladders, scaffolding, ramps, etc.</li>\n <li>Ability to stand for prolonged periods of time (240 minutes)</li>\n <li>Ability to sit for prolonged periods of time (240 minutes)</li>\n <li>Ablity to conduct activities using repetitive motions that include wrists, hands, and/or fingers</li>\n <li>Ability to conduct work that includes moving objects up to 33lbs</li>\n <li>Ability to bend, push or pull, reach to retrieve materials from 18\" to 60\" in height, and use twisting motions. </li>\n <li>Will work in warm/cold environments (0-100F range)</li>\n</ul>\n<p> </p>\n<p>*#LI-Onsite</p>\n<p> </p>\n<p><em>To all agencies: Please, no phone calls or emails to any employee of FUJIFILM about this requisition. All resumes submitted by search firms/employment agencies to any employee at FUJIFILM via-email, the internet or in any form and/or method will be deemed the sole property of FUJIFILM, unless such search firms/employment agencies were engaged by FUJIFILM for this requisition and a valid agreement with FUJIFILM is in place. In the event a candidate who was submitted outside of the FUJIFILM agency engagement process is hired, no fee or payment of any kind will be paid.</em></p>\n<h2>EEO Information</h2>\n<p>Fujifilm is committed to providing equal opportunities in hiring, promotion and advancement, compensation, benefits, and training regardless of nationality, age, gender, sexual orientation or gender identity, race, ethnicity, religion, political creed, ideology, national, or social origin, disability, veteran status, etc.</p>\n<h2>ADA Information</h2>\n<p>If you require reasonable accommodation in completing this application, interviewing, completing any pre-employment testing, or otherwise participating in the employee selection process, please direct your inquiries to our HR Department ([email protected]).</p>",
    "directApply": true,
    "jobLocation": [
      {
        "@type": "Place",
        "address": {
          "@type": "PostalAddress",
          "postalCode": "27709",
          "addressRegion": "NC",
          "streetAddress": "6051 George Watts Hill Drive",
          "addressCountry": "US",
          "addressLocality": "Research Triangle Park",
          "postOfficeBoxNumber": "UNAVAILABLE"
        }
      }
    ],
    "validThrough": "2027-03-30T04:00:00.000Z",
    "employmentType": "OTHER",
    "hiringOrganization": {
      "name": "Fujifilm",
      "@type": "Organization",
      "sameAs": "https://uscareers-fujifilm.icims.com"
    },
    "occupationalCategory": "Quality Control"
  },
  "detail_meta": {
    "url": "https://uscareershub-fujifilm.icims.com/jobs/37362/qc-associate-i%2c-environmental-monitoring/job?in_iframe=1",
    "http_status": 200,
    "content_type": "text/html;charset=UTF-8",
    "response_bytes": 44876,
    "compact_response_bytes": 7915,
    "original_response_bytes": 44876
  },
  "sitemap_job": {
    "id": "37362",
    "url": "https://uscareershub-fujifilm.icims.com/jobs/37362/qc-associate-i%2c-environmental-monitoring/job",
    "slug": "qc-associate-i%2c-environmental-monitoring",
    "lastmod": "2026-04-07T14:58:36-04:00"
  },
  "detail_errors": []
}
Get this page with API

Rendered from the bluedoor Job Postings API. Reproduce it:

GET https://api.bluedoor.sh/job-postings/v1/jobs/8dd0d0b03102a3dfefd8bbb8f1d1d319b2a025e4?include=descriptionJSON
GET https://api.bluedoor.sh/job-postings/v1/orgs/63e98acc-2d53-4b16-a0e9-913c8cd24452JSON
GET https://api.bluedoor.sh/job-postings/v1/sources/6a86663d-e7d5-4a9b-a4c9-cc12544fb1a3JSON
GET https://api.bluedoor.sh/job-postings/v1/jobs/8dd0d0b03102a3dfefd8bbb8f1d1d319b2a025e4/eventsJSON