bluedoor data·Job Postings API·bluedoor.sh ↗

HomeCompaniesUscareers Fujifilm Icims ComSr. Scientist 2, Material Science

Sr. Scientist 2, Material Science

Uscareers Fujifilm Icims Com · Holly Springs, NC, US · Active · iCIMS

Job facts

FieldValue
CompanyUscareers Fujifilm Icims Com
TitleSr. Scientist 2, Material Science
Normalized title-
Department / teamProcess Sciences
LocationHolly Springs, NC, United States
Work model-
Employment typeOTHER
Salary-
Statusactive
ATS provideriCIMS
Posted / first seen2026-04-17 / 2026-05-31
Changed / last seen2026-06-04 / 2026-06-06

Related slices

PageWhat it containsOpen
Company jobsActive postings from Uscareers 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 Holly Springs.Open
Department jobsActive postings in Process Sciences.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

CompanyUscareers Fujifilm Icims Com
Sourcef8d75ae9-789d-4bc9-b0c7-b07ee3fba3e4
ATS provideriCIMS

Description

Position Overview The Sr Engineer or Scientist of Material Science 1 manages the design and development of new single-use consumables in conjunction with our manufacturing teams. This role manages the leachable and extractables program, including organizing testing and creating a data library based on products evaluated. This role also supports manufacturing investigations involving items such as: raw material variability and concerns, consumable issues, particle sources, and provides impact assessments in collaboration with other Process Science subject matter experts (SMEs). Additionally, this role writes investigation reports and leachable and extractable reports. The Sr Engineer or Scientist is the SME for customer and regulatory audits and articulates the Fujifilm Biotechnologies procedures, practices and rationale. Company Overview FUJIFILM Biotechnologies is building the future of bioproduction in Holly Springs, North Carolina. By end of 2025, we’ll open North America’s largest end-to-end CDMO biopharmaceutical manufacturing facility, offering drug substance production, fill-finish, and packaging under one roof. We’re looking for passionate, mission-driven people to help us realize this exciting vision and deliver the next vaccine, cure, or therapy. We offer a dynamic work environment and we’re proud to cultivate a culture that will fuel your purpose, energy, and drive—what we call Genki. Ready to shape the future of medicine? Let’s transform healthcare together! Holly Springs, North Carolina, combines small-town warmth with proximity to Raleigh’s thriving tech scene, making it the perfect blend of community and opportunity. 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 What You'll Do Provides oversight and supports the team with the introduction of new raw materials, and associated document requirements Ensures regulatory compliance, assesses vendor change notifications, and provides strategic input on raw materials related matters Oversees and supports change requests for introduction, modification, and discontinuation of raw materials Acts as a scientific liaison between Quality Control (QC), Supply Chain, Manufacturing, and Quality to assess material and supplier risks (e.g., supplier technical evaluations, risk assessments, raw material evaluation and qualification, and new product introductions) Develops and implements training for manufacturing staff on process improvement initiatives, as needed Leads or coordinates troubleshooting, process impact assessments, and execution of root cause analysis (RCA) and corrective and preventive action (CAPA) in response to critical deviations related to materials used in manufacturing, as needed Delivers documentation for internal and external use, such as comprehensive written protocols and reports, summarizing investigations and impact assessments, studies and projects Supports process sub-teams throughout the phases of technology transfer (TT) Serves as SME to support TT stage gate reviews on incoming processes and manufacturing readiness (e.g., acceptable process material evaluations, risk assessments, mitigation, and robust supporting data for the proposed changes) Provides comprehensive written manufacturing reports summarizing investigations, studies and projects Supports generation of sampling plans for process validation reports (PVRs) and investigations As technical SME, leads and supports generation of master plans, contamination control strategy, extractable and leachable assessment, and other site procedures or policies Collaborates with the Manufacturing department to support commercial and clinical manufacturing campaigns, investigate materials issues, and implement necessary changes Leads continuous improvement projects, in partnership with Manufacturing, Quality, Engineering, and global teams when applicable, to improve manufacturability, reliability, yield and cost Deploys and maintains Large Scale Business Unit (LSBU) strategic roadmap for continuous and breakthrough improvements, and associated requirements Other duties, as assigned Minimum Requirements: Bachelor's degree in Engineering, Life Science or Chemical Engineering with 8 years of relevant experience; or Master's degree in in Engineering, Life Science or Chemical Engineering with 6 years of relevant experience; or PhD with 3 years of relevant experience Experience working in Good Manufacturing Practices (GMP) environment Preferred Requirements: Prior drug substance or manufacturing experience,including expertise in process validation, transfer and commercialization, and manufacturing support and troubleshooting Experience supporting or writing portions of regulatory filings and supporting regulatory audits Direct experience with new product launches and validation of process Experience managing global or multi-site validation programs Physical and Work Environment Requirements: Ability to discern audible cues 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 IDbb465e8b2f178127b0e562bdce651e11370524b0
Org ID51ab77ff-1617-41fc-aaef-c21d6b75e795
Source IDf8d75ae9-789d-4bc9-b0c7-b07ee3fba3e4
Board IDf8d75ae9-789d-4bc9-b0c7-b07ee3fba3e4
Providericims
Provider Job Key37575
TitleSr. Scientist 2, Material Science
Normalized Title
Statusactive
Activeyes
Location TextHolly Springs, NC, US
DepartmentProcess Sciences
Team
Employment TypeOTHER
Workplace Type
Remote Policy
CountryUnited States
RegionNC
CityHolly Springs
Salary RawPosition Overview The Sr Engineer or Scientist of Material Science 1 manages the design and development of new single-use consumables in conjunction with our manufacturing teams. This role manages the leachable and extractables program, including organizing testing and creating a data library based on products evaluated. This role also supports manufacturing investigations involving items such as: raw material variability and concerns, consumable issues, particle sources, and provides impact assessments in collaboration with other Process Science subject matter experts (SMEs). Additionally, this role writes investigation reports and leachable and extractable reports. The Sr Engineer or Scientist is the SME for customer and regulatory audits and articulates the Fujifilm Biotechnologies procedures, practices and rationale. Company Overview FUJIFILM Biotechnologies is building the future of bioproduction in Holly Springs, North Carolina. By end of 2025, we’ll open North America’s largest end-to-end CDMO biopharmaceutical manufacturing facility, offering drug substance production, fill-finish, and packaging under one roof. We’re looking for passionate, mission-driven people to help us realize this exciting vision and deliver the next vaccine, cure, or therapy. We offer a dynamic work environment and we’re proud to cultivate a culture that will fuel your purpose, energy, and drive—what we call Genki. Ready to shape the future of medicine? Let’s transform healthcare together! Holly Springs, North Carolina, combines small-town warmth with proximity to Raleigh’s thriving tech scene, making it the perfect blend of community and opportunity. 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 What You'll Do Provides oversight and supports the team with the introduction of new raw materials, and associated document requirements Ensures regulatory compliance, assesses vendor change notifications, and provides strategic input on raw materials related matters Oversees and supports change requests for introduction, modification, and discontinuation of raw materials Acts as a scientific liaison between Quality Control (QC), Supply Chain, Manufacturing, and Quality to assess material and supplier risks (e.g., supplier technical evaluations, risk assessments, raw material evaluation and qualification, and new product introductions) Develops and implements training for manufacturing staff on process improvement initiatives, as needed Leads or coordinates troubleshooting, process impact assessments, and execution of root cause analysis (RCA) and corrective and preventive action (CAPA) in response to critical deviations related to materials used in manufacturing, as needed Delivers documentation for internal and external use, such as comprehensive written protocols and reports, summarizing investigations and impact assessments, studies and projects Supports process sub-teams throughout the phases of technology transfer (TT) Serves as SME to support TT stage gate reviews on incoming processes and manufacturing readiness (e.g., acceptable process material evaluations, risk assessments, mitigation, and robust supporting data for the proposed changes) Provides comprehensive written manufacturing reports summarizing investigations, studies and projects Supports generation of sampling plans for process validation reports (PVRs) and investigations As technical SME, leads and supports generation of master plans, contamination control strategy, extractable and leachable assessment, and other site procedures or policies Collaborates with the Manufacturing department to support commercial and clinical manufacturing campaigns, investigate materials issues, and implement necessary changes Leads continuous improvement projects, in partnership with Manufacturing, Quality, Engineering, and global teams when applicable, to improve manufacturability, reliability, yield and cost Deploys and maintains Large Scale Business Unit (LSBU) strategic roadmap for continuous and breakthrough improvements, and associated requirements Other duties, as assigned Minimum Requirements: Bachelor's degree in Engineering, Life Science or Chemical Engineering with 8 years of relevant experience; or Master's degree in in Engineering, Life Science or Chemical Engineering with 6 years of relevant experience; or PhD with 3 years of relevant experience Experience working in Good Manufacturing Practices (GMP) environment Preferred Requirements: Prior drug substance or manufacturing experience,including expertise in process validation, transfer and commercialization, and manufacturing support and troubleshooting Experience supporting or writing portions of regulatory filings and supporting regulatory audits Direct experience with new product launches and validation of process Experience managing global or multi-site validation programs Physical and Work Environment Requirements: Ability to discern audible cues 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://uscareers-fujifilm.icims.com/jobs/37575/sr.-scientist-2%2c-material-science/job
Apply URLhttps://uscareers-fujifilm.icims.com/jobs/37575/sr.-scientist-2%2c-material-science/job
First Seen At2026-05-31 18:50:10Z
Last Seen At2026-06-06 08:41:57Z
Last Checked At2026-06-06 08:41:57Z
Last Changed At2026-06-04 14:26:59Z
Inactive At
Source Posted At2026-04-17 04:00:00Z
Source Updated At2026-06-03 16:21:39Z
Raw Payload Uris3://job-postings-prod-raw-590183727216/raw/provider=icims/board=uscareers-fujifilm.icims.com/date=2026-06-06/2026-06-06T08-41-47-834Z-a2cf6860342c6e808a12cf1bd7d1b1c0c4f0254c4c6f43db5a95b437acbed040.json
Event Fields
{
  "content_hash": "b434cc9dabbc1fbfe4a41a14caeeebc21e31ac653b009bb0b873a684e58a0496",
  "source_hash": "b2d2c9b8758520d11e9547d24f2e1dbc444b01efb6c20c99ac5e5f12d6105d9a",
  "last_changed_at": "2026-06-04T14:26:59.075Z",
  "active_status": "active"
}
Parsed Structured
{
  "language": "en",
  "location": {
    "raw": "Holly Springs, NC, US",
    "city": "Holly Springs",
    "region": "NC",
    "country": "United States",
    "is_remote": false,
    "confidence": 0.8
  },
  "salary_max": null,
  "salary_min": null,
  "inferred_at": "2026-06-06T08:41:57.479Z",
  "launch_scope": {
    "reason": "english_us_canada",
    "included": true,
    "language": "en",
    "location": {
      "raw": "Holly Springs, NC, US",
      "city": "Holly Springs",
      "region": "NC",
      "country": "United States",
      "is_remote": false,
      "confidence": 0.8
    },
    "countries": [
      "United States"
    ]
  },
  "remote_policy": null,
  "salary_period": "hour",
  "workplace_type": null,
  "salary_currency": null
}
Extensions
{}
Native Structured
{
  "json_ld": {
    "url": "https://uscareers-fujifilm.icims.com/jobs/37575/sr.-scientist-2%2c-material-science/job",
    "@type": "JobPosting",
    "title": "Sr. Scientist 2, Material Science",
    "@context": "http://schema.org",
    "datePosted": "2026-04-17T04:00:00.000Z",
    "description": "<h2>Position Overview</h2>\n<p>The Sr Engineer or Scientist of Material Science 1 manages the design and development of new single-use consumables in conjunction with our manufacturing teams. This role manages the leachable and extractables program, including organizing testing and creating a data library based on products evaluated. This role also supports manufacturing investigations involving items such as: raw material variability and concerns, consumable issues, particle sources, and provides impact assessments in collaboration with other Process Science subject matter experts (SMEs). Additionally, this role writes investigation reports and leachable and extractable reports. The Sr Engineer or Scientist is the SME for customer and regulatory audits and articulates the Fujifilm Biotechnologies procedures, practices and rationale.</p>\n<h2>Company Overview</h2>\n<p>FUJIFILM Biotechnologies is building the future of bioproduction in Holly Springs, North Carolina. By end of 2025, we’ll open North America’s largest end-to-end CDMO biopharmaceutical manufacturing facility, offering drug substance production, fill-finish, and packaging under one roof.</p> \n<p>We’re looking for passionate, mission-driven people to help us realize this exciting vision and deliver the next vaccine, cure, or therapy. We offer a dynamic work environment and we’re proud to cultivate a culture that will fuel your purpose, energy, and drive—what we call Genki. Ready to shape the future of medicine? Let’s transform healthcare together!</p> \n<p>Holly Springs, North Carolina, combines small-town warmth with proximity to Raleigh’s thriving tech scene, making it the perfect blend of community and opportunity.</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>What You'll Do</strong></p>\n<ul>\n <li>Provides oversight and supports the team with the introduction of new raw materials, and associated document requirements</li>\n <li>Ensures regulatory compliance, assesses vendor change notifications, and provides strategic input on raw materials related matters </li>\n <li>Oversees and supports change requests for introduction, modification, and discontinuation of raw materials</li>\n <li>Acts as a scientific liaison between Quality Control (QC), Supply Chain, Manufacturing, and Quality to assess material and supplier risks (e.g., supplier technical evaluations, risk assessments, raw material evaluation and qualification, and new product introductions)</li>\n <li>Develops and implements training for manufacturing staff on process improvement initiatives, as needed</li>\n <li>Leads or coordinates troubleshooting, process impact assessments, and execution of root cause analysis (RCA) and corrective and preventive action (CAPA) in response to critical deviations related to materials used in manufacturing, as needed</li>\n <li>Delivers documentation for internal and external use, such as comprehensive written protocols and reports, summarizing investigations and impact assessments, studies and projects</li>\n <li>Supports process sub-teams throughout the phases of technology transfer (TT)</li>\n <li>Serves as SME to support TT stage gate reviews on incoming processes and manufacturing readiness (e.g., acceptable process material evaluations, risk assessments, mitigation, and robust supporting data for the proposed changes)</li>\n <li>Provides comprehensive written manufacturing reports summarizing investigations, studies and projects</li>\n <li>Supports generation of sampling plans for process validation reports (PVRs) and investigations</li>\n <li>As technical SME, leads and supports generation of master plans, contamination control strategy, extractable and leachable assessment, and other site procedures or policies</li>\n <li>Collaborates with the Manufacturing department to support commercial and clinical manufacturing campaigns, investigate materials issues, and implement necessary changes </li>\n <li>Leads continuous improvement projects, in partnership with Manufacturing, Quality, Engineering, and global teams when applicable, to improve manufacturability, reliability, yield and cost</li>\n <li>Deploys and maintains Large Scale Business Unit (LSBU) strategic roadmap for continuous and breakthrough improvements, and associated requirements</li>\n <li>Other duties, as assigned</li>\n</ul>\n<p> </p>\n<p><strong>Minimum Requirements:</strong></p>\n<ul>\n <li>Bachelor's degree in Engineering, Life Science or Chemical Engineering with 8 years of relevant experience; or</li>\n <li>Master's degree in in Engineering, Life Science or Chemical Engineering with 6 years of relevant experience; or </li>\n <li>PhD with 3 years of relevant experience</li>\n <li>Experience working in Good Manufacturing Practices (GMP) environment</li>\n</ul>\n<p><strong>Preferred Requirements:</strong></p>\n<ul>\n <li>Prior drug substance or manufacturing experience,including expertise in process validation, transfer and commercialization, and manufacturing support and troubleshooting</li>\n <li>Experience supporting or writing portions of regulatory filings and supporting regulatory audits</li>\n <li>Direct experience with new product launches and validation of process</li>\n <li>Experience managing global or multi-site validation programs</li>\n</ul>\n<p><strong>Physical and Work Environment Requirements:</strong></p>\n<p> </p>\n<ul>\n <li>Ability to discern audible cues</li>\n</ul>\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": "27540",
          "addressRegion": "NC",
          "streetAddress": "100 Biotechnology Ave",
          "addressCountry": "US",
          "addressLocality": "Holly Springs",
          "postOfficeBoxNumber": "UNAVAILABLE"
        }
      }
    ],
    "validThrough": "2027-04-17T04:00:00.000Z",
    "employmentType": "OTHER",
    "hiringOrganization": {
      "name": "Fujifilm",
      "@type": "Organization",
      "sameAs": "https://uscareers-fujifilm.icims.com"
    },
    "occupationalCategory": "Process Sciences"
  },
  "detail_meta": {
    "url": "https://uscareers-fujifilm.icims.com/jobs/37575/sr.-scientist-2%2c-material-science/job?in_iframe=1",
    "http_status": 200,
    "content_type": "text/html;charset=UTF-8",
    "response_bytes": 45106,
    "compact_response_bytes": 7467,
    "original_response_bytes": 45106
  },
  "sitemap_job": {
    "id": "37575",
    "url": "https://uscareers-fujifilm.icims.com/jobs/37575/sr.-scientist-2%2c-material-science/job",
    "slug": "sr.-scientist-2%2c-material-science",
    "lastmod": "2026-06-03T12:21:39-04:00"
  },
  "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/bb465e8b2f178127b0e562bdce651e11370524b0?include=descriptionJSON
GET https://api.bluedoor.sh/job-postings/v1/orgs/51ab77ff-1617-41fc-aaef-c21d6b75e795JSON
GET https://api.bluedoor.sh/job-postings/v1/sources/f8d75ae9-789d-4bc9-b0c7-b07ee3fba3e4JSON
GET https://api.bluedoor.sh/job-postings/v1/jobs/bb465e8b2f178127b0e562bdce651e11370524b0/eventsJSON