Job purpose
You will support operational quality assurance across our Belgium R&D site. You will work essentially with analytical R&D labs and/or GMP clinical manufacturing operations for drug substance, aseptic drug product, or technical services
We offer practical coaching, hands-on experience and clear development paths. You will join a team that values respect, openness, practical problem solving and collaborative working.
This role offers visible impact, learning and career growth while helping GSK unite science, technology and talent to get ahead of disease together.
Responsibilities
This role will provide you the opportunity to support or lead key activities such as :
Provide day-to-day QA oversight for R&D operations related to clinical manufacturing and testing activities to ensure compliance with Good Manufacturing Practice and GSK quality standards including technical services, distribution and supply activities
Review and approve deviations, change controls, CAPA and technical records in a timely and accurate way.
Review and approve qualification and validation activities related to process or equipment
Lead or support investigations and root cause analysis for quality events and ensure robust corrective actions are implemented.
Run self-inspections, support external inspections and drive inspection readiness across R&D activities.
Monitor quality metrics, perform trend analysis and work with teams to deliver local continuous improvements.
Coach and advise cross-functional teams on quality expectations, data integrity and documentation best practices.
This role is on-site in Belgium with occasional hybrid working as agreed with your manager.
Why You?
Basic Qualification
We are seeking professionals with the following required skills and qualifications to help us achieve our goals:
Degree in life sciences, pharmacy, engineering, chemistry or equivalent practical experience.
A previous experience in a regulated pharmaceutical, biotech, or related R&D/manufacturing environment.
Practical knowledge of Good Manufacturing Practice (GMP)
Experience handling deviations, CAPA, change control and technical investigations.
Strong written and spoken English. Knowledge of French or Dutch is an advantage.
Able to work on-site in Belgium and willing to work occasional shifts if required.
Fluency in French in addition to English.
Preferred Qualification
If you have the following characteristics, it would be a plus:
Master’s degree or higher in a relevant science or engineering discipline.
Experience in batch release, product quality review or operational QA in an R&D or small-scale manufacturing context.
Familiarity with electronic quality management systems, electronic batch records or SAP.
Training in root cause analysis, risk assessment or continuous improvement methods.
Experience supporting inspections and responding to audit findings.
Apply now!
If this role fits your skills and ambition, we would love to hear from you.
Application closing date: Tuesday 30 June 2026
Please take a copy of the Job Description, as this will not be available post closure of the advert.
Belgium Salary Range / Fourchette salariale – Belgique: EUR 55,425 to EUR 92,375The 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 the role. In addition, this position may offer an annual bonus and eligibility to participate in our share based long term incentive program which is dependent on the level of the role. More detailed information on the total benefits package will be supplied during the recruitment process. This role is available for applicants from multiple locations, and therefore salary ranges for certain locations are also shown. Salary ranges for other locations are shown because some markets have pay transparency laws that require salary information on job postings, and those locations are potential job sites for this role. If salary ranges are not displayed in the job posting for a specific location or country, the relevant compensation will be discussed during the recruitment process. Please note salaries vary by country based on the candidate’s skills, experience, education level and the market rate for the role. Offers are typically made within the advertised range based on the candidate’s skills, experience and qualifications, with the upper end generally reserved for highly experienced candidates or other exceptional circumstances aligned with these criteria.Le salaire de base mensuel brut minimum pour les nouvelles recrues à ce poste est indiqué ci dessus pour chaque lieu applicable. Ce salaire de base mensuel brut minimum tient compte de plusieurs facteurs, notamment les compétences, l’expérience et le niveau de formation du/de la candidat(e), ainsi que le taux du marché pour le poste. En outre, ce poste peut donner droit à un bonus annuel ainsi qu'une éligibilité pour participer à notre programme de long term incentive basé sur des actions, en fonction du niveau du rôle. Des informations plus détaillées sur l’ensemble du package salarial seront fournies au cours du processus de recrutement. Ce poste étant ouvert à des candidat(e)s basé(e)s dans plusieurs pays, des fourchettes de salaire sont également indiquées pour certains lieux. Les fourchettes salariales pour d'autres localisations sont mentionnées parce que certains marchés ont des lois en matière de transparence salariale qui imposent que les informations sur les salaires soient affichées dans les offres d’emploi, et que ces pays sont des lieux potentiels pour ce poste. Si aucune fourchette salariale n’est indiquée dans l’offre d’emploi pour un lieu ou un pays spécifique, la rémunération correspondante sera discutée au cours du processus de recrutement. Veuillez noter que les salaires varient selon le pays en fonction des compétences, de l'expérience, du niveau de formation du/de la candidat(e) et du taux du marché pour le poste. Les offres sont généralement faites dans la fourchette annoncée en fonction des compétences, de l'expérience et des qualifications du/de la candidat(e), la partie haute de la fourchette étant généralement réservée aux profils très expérimentés ou à des circonstances exceptionnelles répondant à ces critères.
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 purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases – to impact health at scale.
People and patients around the world count on the medicines and vaccines we make, so we’re committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.
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