QA Specialist, DSM (Project QA) jobs in United States
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FUJIFILM America · 7 hours ago

QA Specialist, DSM (Project QA)

FUJIFILM Biotechnologies is building the future of bioproduction in Holly Springs, North Carolina, and they are seeking a QA Specialist for Drug Substance Manufacturing. This role is responsible for quality oversight of DSM project processes, ensuring systems are maintained in a validated state, and providing support for day-to-day operations and issue resolution.

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H1B Sponsor Likelynote

Responsibilities

Performs a role within the QA team for the development of documents, processes, and procedures for the DSM program
Generates, reviews, and approves QA procedures for the validation approach and lifecycle documents for Manufacturing Systems
Provides QA oversight and supports DSM operations in accordance with governing processes and procedures
Provides QA support of DSM tasks such as Batch Record and Solution Lot Record review, including exception-based oversight using Quality Review Management tool
Real time event triage and implementation of immediate response to identified deviations
Area changeover and return to service
Real time WO oversight per applicable procedures
Ensures department objectives are met within desired timelines and/or in accordance with identified KPIs
Contribute to the development of QA documentation, procedures, and processes for operational readiness objectives and QA support of manufacturing operations in cGMP regulated facility
Participate in streamlining or efficiency improvement initiatives with other FUJIFILM Biotechnologies sites
Perform other duties, as assigned

Qualification

GMP Quality AssuranceValidationCGMP manufacturingFDA regulationsASTM E2500SmartsheetTrackwiseMasterControlKneat validation softwareLife Sciences degreeEngineering degreeSoft skills

Required

BS/BA in Life Sciences or Engineering or equivalent with 2+ years of relevant experience OR
Masters in Life Sciences or Engineering or equivalent with 0 years' relevant experience
1-3 years' experience in a GMP environment
Experience in Validation, cGMP manufacturing operations and/or Quality oversight, in an FDA regulated facility

Preferred

2+ years of experience in GMP Quality Assurance and/or similar role
Experience and working knowledge of ASTM E2500, Smartsheet, Trackwise, MasterControl and/or Kneat validation software

Company

FUJIFILM America

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For over 90 years, Fujifilm has found #ValueFromInnovation through expanding its portfolio to represent a broad spectrum of industries including medical and life sciences, electronic, chemical, graphic arts, information systems, industrial products, broadcast, data storage, and photography.

H1B Sponsorship

FUJIFILM America has a track record of offering H1B sponsorships. Please note that this does not guarantee sponsorship for this specific role. Below presents additional info for your reference. (Data Powered by US Department of Labor)
Distribution of Different Job Fields Receiving Sponsorship
Represents job field similar to this job
Trends of Total Sponsorships
2025 (3)
2022 (2)

Funding

Current Stage
Late Stage
Total Funding
unknown
2006-06-13Acquired

Leadership Team

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Deepak Mahulikar
Chief Technology Officer
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Patrícia Colombo
Chief Compliance Officer
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Company data provided by crunchbase