LES Laboratory Equipment Connectivity Specialist

Job description

Nombre del sítio: Belgium-Wavre
Fecha de publicación: Feb 21 2024

This position lead oversees LES Equipment connectivity design and implementation, ensuring that business needs are well defined, and implementation have followed QA and data integrity guidance.

The position includes best practices sharing with QC Be Laboratories, LBPO LES, LES SME, LES admin and Global QC.

Covered scope is QC Belgium for LES Laboratory connectivity definition, implementation & support

In this role you will…

·  Translate Business needs linked to LES equipment connectivity, standardisation while ensuring quality requirements are met
·  Coordination, planning, testing and execution of lab equipment Connection (SDMS/Lantronix/File Service/OneCDS) to the LES
·  Equipment connectivity documentation management (report) and execution of data extraction needed for parsing activity.
·  Collaborate with and support appropriate stakeholders (Business, QA, equipment validation team, LBPO LES, LES SME, Key users, LES admin, GQC, integration and Lab computers support teams) locally.
·  Manage eCC for his/her scope of responsibilities. Contribute in the post interfacing support (e.g. support issue during data transfer to the LES, bug LabWare) and live cycle, management of risks and opportunities linked to LES in QC Labs
·  Support LBPO LES in the analysis of BE Site roles assignment
·  Contribute to trackers tools and KPI on LES equipment connectivity and follow up

This job opportunity is a permanent contract not opened for relocation.

Why you?

Qualifications & Skills:

·  Bachelor degree or Master university degree
·  At least 3 years of experience in Pharmaceutical Manufacturing, R&D or Quality Control Environment
·  Computer skills in excel, word, outlook, PowerPoint
·  Experience in pharmaceuticals or IT environment
·  Knowledge in equipment validation process
·  Demonstrates project management skills
·  Good interpersonal and influencing skills, communication skills, strong collaborator/communicator;
·  Working experience in a GxP regulated environment
·  Compliance minded
·  Effective time management, ability to clearly identify priorities and manage multiple tasks
·  Ensures efficient and collaborative partnership with operational colleagues as well as with key stakeholders
·  Fluent in French and independent in English. Other international languages are considered as an asset.

Preferred Qualifications & Skills:

·  Participates in establishing the project team.; clearly defines roles, responsibilities and individual objectives
·  Works in cooperation with the entities concerned and helps them to understand project impact
·  Communication skills to build relationships based on trust within project team and outside
·  Internal and external network development in order to ease and accelerate projects’ progress
·  Communicate customers & stakeholders in a manner which is always clear, concise, well-structured and easily understood, using the most appropriate communication channels to inform on progress made
·  Key stakeholders can be outside QC Belgium (e.g.: R&D as QC Belgium give also the support to R&D for Infrastructure and Equipment management)
·  Is aware of the value of the contribution of others
·  Promote teamwork to establish consensus among team members

*Li-GSK

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Why GSK ?

GSK is a global biopharma company with a special purpose – to unite science, technology and talent to get ahead of disease together – so we can positively impact the health of billions of people and deliver stronger, more sustainable shareholder returns – as an organisation where people can thrive. Getting ahead means preventing disease as well as treating it, and we aim to impact the health of 2.5 billion people around the world in the next 10 years.

Our success absolutely depends on our people. While getting ahead of disease together is about our ambition for patients and shareholders, it’s also about making GSK a place where people can thrive. We want GSK to be a place where people feel inspired, encouraged and challenged to be the best they can be. A place where they can be themselves – feeling welcome, valued and included. Where they can keep growing and look after their wellbeing. So, if you share our ambition, join us at this exciting moment in our journey to get Ahead Together.

Si tiene una discapacidad y necesita asistencia durante el curso del proceso de selección, tendrá la oportunidad de hacernos saber qué asistencia específica necesita para hacer los arreglos adecuados.

Nuestro objetivo es ser una de las empresas de atención médica más innovadoras, de mejor desempeño y más confiables del mundo. Creemos que todos aportamos algo único a GSK y cuando combinamos nuestros conocimientos, experiencias y estilos, el impacto es increíble. Únase a nuestra aventura en GSK donde se inspirará para hacer el mejor trabajo para nuestros pacientes y clientes. Un lugar donde puede ser usted mismo, sentirse bien y seguir creciendo.

    

Aviso importante a las empresas o agencias de empleo

GSK no acepta recomendaciones de empresas de empleo o agencias de empleo con respecto a las vacantes publicadas en este sitio. Todas las empresas o agencias de empleo están obligadas a ponerse en contacto con el Departamento de Contrataciones Comerciales y Generales o el Departamento de Recursos Humanos de GSK para obtener autorización previa por escrito antes de recomendar a cualquier candidato a GSK. La obtención de autorización previa por escrito es una condición precedente a cualquier acuerdo (verbal o escrito) entre la empresa o agencia de empleo y GSK. En ausencia de dicha autorización por escrito, se considerará que las acciones que emprenda la empresa o agencia de empleo se han realizado sin el consentimiento o el acuerdo contractual de GSK. Por lo tanto, GSK no será responsable de ninguna tarifa derivada de tales acciones o cualquier tarifa que surja de cualquier recomendación por parte de las empresas o agencias de empleo con respecto a las vacantes publicadas en este sitio.