QA Specialist, DSM (Project QA) jobs in United States
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FUJIFILM Biotechnologies · 8 hours ago

QA Specialist, DSM (Project QA)

FUJIFILM Biotechnologies is building the future of bioproduction in Holly Springs, North Carolina. The QA Specialist, Drug Substance Manufacturing (DSM) is responsible for quality oversight of DSM project processes, ensuring that systems and processes are maintained in a validated state throughout their lifecycle.

BiotechnologyHealth CareManufacturing
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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 regulated facilityASTM E2500SmartsheetTrackwiseMasterControlKneat validation softwareLife Sciences

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 Biotechnologies

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For over 30 years, FUJIFILM Biotechnologies' mission has been advancing tomorrow’s medicine.

H1B Sponsorship

FUJIFILM Biotechnologies 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
2021 (1)

Funding

Current Stage
Late Stage

Leadership Team

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Lars Petersen
President & Chief Executive Officer
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Morten Munk
Director - Global Alliance Management
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Company data provided by crunchbase