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LIMS Templator / LIMS Data Entry

Reference:JSC00032350 Location: Dublin
Qualification:DegreeExperience:See description
Job Type:Fixed Term ContractSalary: Not Disclosed
May be suitable for: Data Management

We’re currently recruiting for an exciting opportunity with an award-winning pharmaceutical organization based in Dublin. This is an excellent position for anyone who is looking to join a leading multinational who are one of the best at what they do.

The Laboratory Information Management System (LIMS) Upgrade project requires LIMS Templators / LIMS Data Entry resources to support the data migration, LIMS templating and data entry efforts under the guidance and direction of the Business Workstream Lead and Project/Program Management.

• Work within the LIMS Modernization Project Team to provide laboratory business administration, implementation and technical support services for SM-LIMS, Biovia Smartlab (LMES) and Biovia CIMS (Inventory Management).

• Review of Quality Documentation e.g. Sample Plans, FORMs and Environmental Monitoring sample plans, Methods, Specifications to:
o Build, develop and maintain LIMS templates.
o Evaluate new or revised LMES eProcedures in conjunction with SMEs.
o Provide support for LMES eProcedure revisions
o Provide support for CIMS updates

• Work with the Documentation Writers to:
o Provide support for SOP updates.
o Assist with developing and deliver training documents.
o Assist with UAT script writing

• Be responsible for specific tasks within several workstreams associated to the LIMS Modernization Upgrade project.
Ensure timely completion of each stage of the Project Tasks
Ensure flow of communication to stakeholders.

Key Competencies:

• Apply analytical thinking to evaluate and interpret complex situations/problems using multiple sources of information.
• Excellent verbal and written communication skills including technical writing, presentation and facilitation skills.
• Work collaboratively with global business team
• Ability to work under minimal supervision.
• Ability to work in a fast paced environment with changing priorities.
• Excellent Organizational and Time Management Skills.
• Ability to identify and manage competing priorities.
• Anticipate and prevent potential problems.
• Skills in the areas of teamwork, flexibility, coaching and motivating.

Knowledge and Experience:

• Hold a third level qualification in a Science related discipline.
• Minimum 4 years experience in a Biotechnology/ Pharmaceutical/ GMP Environment.
• Familiar with (or can learn) new laboratory information systems and can self-teach technical topics.
• Familiar with system validation of computerized systems.
• Familiar with SQL querying, excel logic, java or html is a plus.
• Knowledge of lab operations, analytical lab techniques, commercialization, and cGMP.
• Knowledge on Data Integrity Assessments (DIA) for computerized systems and execution of CFR 21 Part 11 for computerized systems.
• Experience as a user (as a minimum) of LIMS System

Any applicant must be eligible to work in Ireland. Existing work permit or EU passport required. No visa sponsorship will be offered with this role. Contact Jack Caffrey at for more details.