eLIMS Coordinator | GMP | Leiden, NL

Location: Netherlands

SIRE® is the market leader in Life Sciences recruitment. We believe the recruitment market needs to gear up in technology and continuous innovation. We like technology, in a Life Sciences market driven on science, we couldn’t stay behind; we drive Recruitment Science. Investing a majority of our turnover in technology enables us to use unique Resource Technologies. By using highly advanced algorithms, we enable our team of Resource & Data Strategists© to maintain the most advanced, detailed and complete Life Sciences network in Europe. This big data enables us to work Reverse Recruitment©: we first analyze the market in-depth before we go out to the market. Because we analyze the whole market, we can compare facts and data. This enables us to do Facts & Big Data Recruitment©, making sure we, or better yet, you find the right career!Our client is a professional Pharmaceutical and Biotechnology organisation, based in Zuid-Holland Netherlands.

The Company

Janssen Vaccines is committed to developing first-in-class or best-in-class vaccines for some of the world’s most life-threatening infectious diseases. We have built a dedicated, world-class, multi-functional team across a variety of disciplines to develop a promising vaccines pipeline. In Leiden, we have a workforce of 700 scientists and support staff, 45% of our employees has a nationality other than Dutch with over 20 nationalities represented. We partner with many of the world’s leading experts, academic and clinical institutions and other pharmaceutical companies for the development of vaccines against, for example, Ebola and HIV.

Role Description

We are searching for a suitable candidate to reinforce our multidisciplinary team as eLims coordinator with main focus on support to our release and stability process of our vaccines. As eLims coordinator you have a wide knowledge of electronic laboratory information management systems within a quality control department of a pharmaceutical company. You will combine your experience in quality control testing and eLims knowledge to not only maintain but also improve the digital processes that support our labs. You will translate business needs into eLims functional processes and have an important role to ensure availability of our vaccines for clinical trials and the patients.

Responsibilities

o master data configuration and approval;
o global contact person for the site;
o Provide technical help in troubleshooting eLIMS application related issues;
o General system admin responsibilities, configuring user access and roles;
o Troubleshoot incidents/issues with LIMS and follow through to resolution;
o Create, update, and maintain all standard operating procedures, (local procedures) relevant to eLIMS;
o R&S/QCD Coordination assistance;
o KPI dashboards creation (spotfire);
o Initiate eLims improvement projects;
o Cross departmental contact;
o Giving training on eLims use;
o Develop documentation and execute testing when required.

Requirements

MBO4 + a minimum of 5 years of experience in a GMP laboratory environment OR a BSc. with a minimum of 2 years of lab experience in Analytical Chemistry, Biotechnology, Life Sciences or related fields;
• Minimum of 2 years of experience with digital Data Management Systems configuration (preferably eLims);
• Experience in a development GMP environment.

Other information

You will be offered a year contract, followed by a permanent contract. Full time is preferred, but 32 hours per week is discussable.

Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Cees Roffelsen.