Site Name: Belgium-Wavre
Posted Date: Sep 6 2024
This is a great opportunity to join the team as Supervisor QC Support Testing.

Your key responsibilities will be:

• You contribute to lab testing by aligning material and human resources and skills
  
• You work in collaboration with a First Line Leader to manage a team of Laboratory Technicians (train and develop the team, plan, prioritize and control laboratories activities, manage the resources and proactively anticipates resources needs)
  
• A term, you will have the possibility of management of a lab team (7-10 technician for laboratory testing)
  
• You ensure the performance and commitment of the team in order to achieve production objectives while guaranteeing EHS, Quality, Costs and Supply requirements
  
• You release of commercial lots, testings for stability studies : Assures the efficiency of Quality Control (quality, delay, results interpretation, KPI) and releases results of tests conducted in his/her laboratory
  
• You perform follow-up of experiments with laboratories and collect data
  
• You ensure the quality of results provided by the Laboratory team
  
• You write reports and submit the reports for review and approval
  
• You are responsible for the validation of new reagents and participation to the validation of analytical methods
  
• You follow-up of the quality system used in the laboratory and reagents follow-up
  
• You are responsible for the management of Laboratory and availabilility of associate equipments
  
• You perform critical review of analytical data
  
• You are responsible for Quality documentation writing (deviations, CAPA, procedures, protocols, reports …).
  
• You have transversal interactions with other teams in QC, with QA and different MPU : Guarantee good communication for transversal interactions.
  

Why you?

Basic qualifications:

• Master degree / engineer with an experience in pharmaceutical area
  
• Scientific background in analysis of Physicochemistry tests
  
• Pratical and theoretical knowledges in the domain of laboratory activities (tests : HPLC/UPLC/GC, spectrophotometry …)
  
• Theoretical knowledge of GMP (practical knowledge is an asset)
  
• Experience in the field of analytics and quality control
  
• French (fluent is mandatory) and English (spoken and written)
  

Preferred Qualifications:

If you have the following characteristics, it would be a plus:

• Ph D in Physicochemistry/Biotechnology or equivalent
  
• Data management: DMAIC approach knowledge is an asset.
  
• Knowledge of deviation process is an asset
  
• Experience in Pharmaceutical area is a plus
  

If you have a disability and require assistance during the course of the selection process, you will have the opportunity to let us know what specific assistance you require in order to make suitable arrangements.

Why GSK?
Uniting science, technology and talent to get ahead of disease together.

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. We prevent and treat disease with vaccines, specialty and general medicines. We focus on the science of the immune system and the use of new platform and data technologies, investing in four core therapeutic areas (infectious diseases, HIV, respiratory/ immunology and oncology).

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.

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