GSK
SupervisorQC(1yearfixedcontract)
Neural analysis suggests this role is
optimal for Mid+ candidates.
“Supervisor QC (1 year fixed contract) at GSK. Skills: process management, cross-functional coordination, vendor/stakeholder management, operational metrics, resource planning, continuous improvement. Management of a logistic operator team (around 5 people). Responsibility of the laboratory and the follow-up of the equipments”
Industry & Context.
1 year fixed contract
What They're Looking For.
Must Have
Experience in people management, Practical and theoretical knowledges in the domain of laboratory in vivo activities, Theoretical knowledge of GMP, Experience in the field of analytics and quality control, French (fluent is mandatory) and English (spoken and written)
Nice to Have
Experience in the field of laboratory animal science and in in Pharmaceutical area is a plus, Knowledge of deviation & CAPA process is an asset, Practical and theoretical knowledges in the domain of laboratory in vivo activities is an asset
What You'll Do.
Management of a logistic operator team (around 5 people)
Responsibility of the laboratory and the follow-up of the equipments
Ensure the daily organization of the activities of the team
Management of logistic activities (management of the supply of stock/orders
follow-up of equipments)
Quality documentation management (deviations
Ensure EHS rules are applied
Ensure compliance with EHS
quality and ethics rules/guidances
Ensure good management of the area
Ensure the monitoring of environmental parameters and alarms
Participate in the follow-up of the maintenance and validation of the equipment in the area
Participate to implementation of logistic’s projects (paperless
new “prep mat” organization
task frequencies review
How You'll Work.
Team & Collaboration
Transversal interactions with other teams (internal customers/ support teams)
Full Job Description
# **This is a fixed term contract of 1 year** # # **About the role** * Management of a logistic operator team (around 5 people) * Responsibility of the laboratory and the follow-up of the equipments # **About the responsibilities** * Ensure the daily organization of the activities of the team * Management of logistic activities (management of the supply of stock/orders, follow-up of equipments) * Quality documentation management (deviations, CAPA, procedures, …) * Transversal interactions with other teams (internal customers/ support teams) * Ensure EHS rules are applied * Ensure compliance with EHS, quality and ethics rules/guidances * Ensure good management of the area * Ensure the monitoring of environmental parameters and alarms * Participate in the follow-up of the maintenance and validation of the equipment in the area * Participate to implementation of logistic’s projects (paperless, new “prep mat” organization, task frequencies review,…) * Ensure the daily organization of the activities of the team # **About you** * Experience in people management * Practical and theoretical knowledges in the domain of laboratory in vivo activities * Theoretical knowledge of GMP * Experience in the field of analytics and quality control * Experience in the field of laboratory animal science and in in Pharmaceutical area is a plus * French (fluent is mandatory) and English (spoken and written) * Knowledge of deviation & CAPA process is an asset. * Practical and theoretical knowledges in the domain of laboratory in vivo activities is an asset **Please take a copy of this job description as it won 't be available after the posting** #GSKVaccines #LI-GSK Belgium Salary Range / Fourchette salariale – Belgique: EUR 53,325 to EUR 88,875 The annual gross base salary range for new hires in this position is listed above for each applicable location. These ranges take into account a number of factors including the candidate’s skills, experience, education level and the market rate for
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