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Specialist Quality Control LIMS

FUJIFILM Diosynth Biotechnologies
Thousand Oaks, CA Full Time
POSTED ON 3/19/2025
AVAILABLE BEFORE 4/17/2025
The Specialist, Quality Control supports Fujifilm Diosynth Biotechnologies California (FDBC) QC with the business analysis, design, development, implementation, validation, and support of existing and new Laboratory Information Management Systems (Labware LIMS) and other lab applications. The Specialist, Quality Control is a customer facing role, working in close collaboration with Quality Control (QC), Quality Assurance, Manufacturing, and Information Technology (IT) teams. The Specialist will follow FDBC methodologies for systems and project governance, leverage tools & techniques to capture business and functional requirements and use approved corporate documentation templates and systems for software development lifecycle documentation.

Company Overview

Join us! FUJIFILM Diosynth Biotechnologies is advancing tomorrow’s medicine, impassioning employees to chase the impossible and continually expand their potential. We are a company of emboldened goal seekers – driven by an innate desire to better ourselves, our families, our workplace, our company, our community, and the world at large.

Job Description

Reports to: Senior Manager, QC

Location: Thousand Oaks (northwest Los Angeles area)

Travel: 10%

Primary Responsibilities:

  • Plan and implement the design, configuration and/or customization of LIMS according to business requirements. (i.e., Configure Analysis, Sample Plan and Product Specification, Electronic Lab Notebook (ELN) Templates, calculations etc. in Labware LIMS for New Products Introduction)
  • Lead optimization of LIMS activities in collaboration with functional areas, which include defining LIMS workflows, maintain dynamic/static data in LIMS, perform and participate in GMP review, LIMS Access review and internal/external audits.
  • Evaluate product enhancements and capabilities as required.
  • Fully lead, manage, and own project implementations.
  • Triage, delegate and manage the LIMS project deliverables and priorities with cross-functional leads.
  • Work with subject matter experts (SMEs) to clarify and document user requirements. Create and maintain application procedures and system configuration documents. Author and review SOP’s.
  • Translate functional business requirements into technical requirements and specifications. Ensure project deliverables meet business requirements
  • Own Quality Management System records (Deviations, CAPAs, Change Control’s) to completion.
  • Support creation, review and executing system validation documentation (IQ, OQ and PQ) and change control documentation.
  • Serve as a point of contact for LIMS and provide support and training on LIMS to end users for any new enhancements or major changes implemented in LIMS.
  • Responsible for management of equipment and supplies related to LIMS, which includes vendor coordination, setting up printers, ordering supplies for printers.

Qualifications:

  • Bachelor of Science or Engineering in Computer Science / programming and/or similar field with 5 years of experience or an equivalent combination of education; or Master of Science (M.Sc.) with 3 years of experience; or PhD in Science with 0-3 years of experience.
  • Advanced knowledge of LIMS software / configuration/ system usage, and/or laboratory experience. Experience with Labware LIMS version 7.0 or greater software is a plus. Experience with Product lot management, Environmental Monitoring and Stability samples in LIMS is a plus.
  • Working knowledge of document management and lifecycle
  • Working knowledge of quality systems and their interconnections (e.g., LIMS and document revisions)
  • Advanced knowledge of sampling plan lifecycle and inventory management
  • Basic knowledge of product testing, data analysis, and reporting.
  • Working knowledge of Validation Life Cycle and knowledge of GAMP, GDP’s (GCP, GLP, and GMP), 21-CFR Part 11 regulation of Electronic Records, Electronic Signatures, and Audit Trails.
  • Advanced knowledge of Quality Management System (CAPA, deviation, change control)
  • Basic knowledge in Reporting software program is a plus (Power BI or Tableau or Crystal Reports).
  • Basic knowledge of Lab-associated systems (Empower) and/or ERP Systems (SAP, Oracle)

Salary and Benefits:

  • $104,000-$130,000, depending on experience
  • Medical, Dental and Vision
  • Life Insurance
  • 401k
  • Paid Time Off

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 (FDBCHR@fujifilm.com).

Salary : $104,000 - $130,000

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