drjobs Senior Specialist Quality Control LIMS

Senior Specialist Quality Control LIMS

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1 Vacancy
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Job Location drjobs

Thousand Oaks, CA - USA

Monthly Salary drjobs

$ 130000 - 160000

Vacancy

1 Vacancy

Job Description

Position Overview

The Sr. 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 Sr. 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 Sr. 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 tomorrows 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 crossfunctional 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 SOPs.
  • Translate functional business requirements into technical requirements and specifications. Ensure project deliverables meet business requirements
  • Own Quality Management System records (Deviations CAPAs Change Controls) 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 7 years of experience or an equivalent combination of education; or Master of Science (M.Sc. with 5 years of experience; or PhD in Science with 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 GDPs (GCP GLP and GMP) 21CFR 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 Labassociated systems (Empower) and/or ERP Systems (SAP Oracle)

Salary and Benefits:

  • $130000 to $160000 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 viaemail 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.



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EEO Information

Fujifilm is committedto 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 preemployment testing or otherwise participating in the employee selection process please direct your inquiries to our HR Department .


Required Experience:

Senior IC

Employment Type

Unclear

Company Industry

Department / Functional Area

Quality Control

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