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Senior LIMS Analyst - EQMS

FUJIFILM Diosynth Biotechnologies
College Station, TX
Start date
Aug 6, 2022

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Job Details

Summary:  The Sr. LIMS Analyst will be the Quality organization's Subject Matter Expert (SME) as it relates to the configuration, implementation, analysis as well as the maintenance of the (eQMS) across multiple facilities.

External US

Essential Functions:

  • Member of a team responsible for coordinating and executing all activities necessary to maintain compliance with cGMP and/or ISO 13485 and the integrity of the Quality Management System
  • Develop and maintain eQMS installation and configuration management procedures.
  • Following up on support issues proactively to provide timely updates and resolutions to end users.
  • Provide troubleshooting expertise to end users on an ad hoc basis, consulting with the software vendor(s) as needed. Work with the vendor to troubleshoot and resolve application issues. Coordinate and communicate with impacted stakeholders as needed.
  • Provide quality oversight and compliance support to implement and validate electronic systems in accordance with the corporate computer system validation (CSV) procedures and requirements
  • Develop or review protocol, plans, scripts, reports, SOPs etc. associated with the implementation and maintenance of computerized systems
  • Provide QA oversight during risk, Part 11 and Annex 11 and regulatory assessments
  • Represent the eQMS group at cross-functional meetings
  • Review changes to validated state of system through the change control and participate in planning and implementing changes
  • Serve as the QA contributor on projects including inquiries pertaining to the interpretation of the FDA and other regulatory requirements for computer system validation
  • Perform other quality and computer system validation duties as assigned
  • Stakeholder in the development, implementation, and continued improvement of quality systems within the QA department.
  • Execute document and change control processes to ensure standardization, accuracy, and completeness of documents prior to release.
  • Maintain controlled copies of Quality documents in the files and in electronic databases
  • Facilitate document retrieval during regulatory inspections.
  • Participate in cross-functional teams comprised of laboratory, materials management, EH&S, and Quality personnel across multiple sites to expand and improve the use of the LIMS system and to design and implement added-value applications within the LIMS and other local or global lab informatics environments.
  • Implement the LIMS workflows and reports to meet business needs.
  • Manage the administration and implementation of the LIMS and all QC instrument software following client policies.
  • Administer accounts, roles, and system functions per global and local LIMS procedures.
  • Solve end-user LIMS template and end-user LIMS data entry issues.
  • Work with IT and Quality personnel to ensure system compliance.
  • Develop and execute validation scripts as needed for change control issues.
  • Identify operational improvement opportunities which LIMS can provide solutions.
  • Define project scope, goals and deliverables that support business goals in collaboration with senior management and stakeholders.
  • Develop new SOP's and/or revise existing SOPs; write deviations, CAPA's, and Change Controls as needed as well as developing specific LIMS SOPs
  • Perform other duties as assigned.

Required Skills & Abilities:

  • Self-motivated with a drive for excellence
  • Positive attitude and strong interpersonal skills
  • Honesty, integrity, respect and courtesy with all colleagues
  • Creative and can work with minimal supervision following internal procedures balanced with independent thinking
  • Resilient through operational and organizational change
  • Exceptional planning and organizational skills and the ability to multi-task and meet deadlines is required
  • Requires the ability to communicate effectively using speech, vision, hearing and written word
  • Must be able to walk or move or drive between locations
  • Interacts with all departmental staff, including giving training and / or presentations to small and large groups
  • Apply knowledge of cGMPs on a daily basis, as applicable
  • Adhere to the standards of quality ruled by current GMP and the company Quality Policies and site SOPs
  • Ability to accurately complete required documentation
  • Excellent organization, detail oriented and accurate
  • Knowledge of MS Office (Word, Excel, Outlook)

Preferred Experience, Skills & Abilities:

  • Ability to multi-task and prioritize work assignments with little supervision.
  • Experience with Quality System investigations and other concepts (Deviation, OOS, CAPA, Change Control, Audits, etc.).
  • Experience with MasterControl/Trackwise/LIMS/MODA etc is a plus
  • Experience in developing cGMP training materials is preferred
  • Must have working knowledge of FDA (21CFR 210, 211 & 820) and EU regulatory requirements
  • Previous experience implementing or administration of an eQMS software system is necessary

Working Conditions & Physical Requirements:

The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job.  Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.  While performing the duties of this job, the employee is regularly required to:

  • Must be willing to work flexible hours
    • Experience prolonged standing, some bending, stooping, and stretching
    • Ability to sit for long periods to work on a computer
    • Use hand-eye coordination and manual dexterity sufficient to operate a keyboard, photocopier, telephone, calculator, and other office equipment is required
    • Attendance is mandatory



  • B.S. Degree in Biology, Chemistry, Engineering, Information Technology or related discipline and 5-7 years' experience in the pharmaceutical/biotechnology industries.
  • Experience with LIMS is required.
  • Experience with LabWare is required.
  • Must have superior database maintenance/development experience.
  • Familiarity with a variety of lab equipment
  • Proficient computer skills.
  • Excellent documentation skills.
  • Strong technical aptitude for problem solving and data driven decision making.


FUJIFILM Diosynth Biotechnologies is an industry leading cGMP Contract Development and Manufacturing Organization (CDMO) supporting our partners in the biopharmaceutical industry with the development and production of their biologic, vaccines and gene therapies.

With over 30 years of experience in process development and cGMP manufacturing, a dedicated staff of over 2,000 and a reputation for excellent customer service, flexibility and responsiveness, we’ve become a trusted partner to some of the most prominent biotech developers and pharmaceutical companies in the industry.

Our Process Development experience includes the development of processes for molecules expressed via fermentation (e.g., E. coli, P. pastoris), cell culture systems including CHO, HEK, Vero, MDCK, EB66 and insect cells, and from transgenic sources.

Our network expands within five development and manufacturing facilities located in Teesside, United Kingdom; Research Triangle Park, North Carolina, USA; College Station, Texas, Thousand Oaks CA USA and Hillerød, Denmark.


Find Us
Thousand Oaks, CA
Research Triangle Park, NC
College Station, TX
Holly Springs, NC
Watertown, MA
United States
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