LIMS Templator / LIMS Data Entry
This job does not exist anymore.
Try running a new searchor browse our vacancies.
Or fill in the form below to receive job alerts.
| Job Type | Contractor |
| Area | Dublin, Ireland |
| Sector | Laboratory/Scientific |
| Start Date | |
| Advertiser | Mary King |
| Job Ref | 1002821 |
| Job Views | 63 |
- Description
- Team Horizon is seeking a LIMS Templator / LIMS Data Entry for our client based in Dublin on a 6-months contract. 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.
Why you should apply:
This is an excellent opportunity to join a world class manufacturing operation, with an outstanding track record of reliably delivering high-quality medicines to patients around the world suffering serious illnesses.
There is a strong culture of continuous improvement and innovation within the company to strive for solutions that improve health outcomes and dramatically improve people’s lives.
Our client is developing the capability to produce all its medicines in Dublin, helping to ensure continuity of supply of our medicines as they expand internationally.
What you will be doing:
Review of Quality Documentation e.g. Sample Plans, FORMs and Environmental Monitoring sample plans,
Evaluate new or revised LMES eProcedures in conjunction with SMEs.
Provide support for LMES eProcedure revisions
Provide support for CIMS updates
Work with the Documentation Writers to provide support for SOP updates.
Assist with developing and deliver training documents.
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
What you need to apply:
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
