Job Summary The successful candidate will play a key role in analysing and optimising our current test documentation processes. You will work closely with laboratory technicians to understand their needs and identify opportunities for digitalisation. Your goal will be to propose and implement digital solutions that meet these needs while ensuring compliance with regulatory requirements.

Key Responsibilities

• Analyse current test documentation processes and identify areas for improvement
• Collaborate with laboratory technicians to understand their needs and gather requirements
• Propose and implement digital solutions to optimise test documentation
• Develop a plan for implementation and validate the proposed solution
• Participate in testing and training users on the new system
• Ensure clear communication around changes introduced

Requirements

• Currently studying for a Bachelor's or Master's degree in a relevant field (data analysis, business analytics, management, economics, computer science, or related field)
• Fluent in French and proficient in English (technical English reading skills a minimum requirement)
• Familiarity with quality norms, GMP, and document integrity
• Experience with data structuring, versioning, and validation workflows
• Basic knowledge of laboratory environments and data management systems

What We Offer

• The opportunity to gain valuable work experience in a global biopharma company
• A chance to contribute to improving the health of millions of people worldwide
• A dynamic and supportive work environment

Duration and Location

• 4-6 month internship
• On-site work required (GSK Wavre, Belgium), with occasional remote work possible

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As an intern, you will work on production operations, respecting quality and safety standards, and collaborate with technicians, supervisors, and quality teams.

Key responsibilities:

• Perform and document production steps according to quality procedures
• Execute technical manipulations (filling, filtration, purification or process operations)
• Follow and complete check-lists and batch records accurately
• Participate in investigations of deviations and alert hierarchy in case of anomalies
• Collaborate with support teams (QA, maintenance, logistics) to ensure operation continuity
• Propose and contribute to improvement actions for procedures and work tools

Requirements:

• Currently studying for a Master's degree in Sciences (chemistry, biochemistry, biology, agronomy, pharmacy or equivalent)
• Fluent in French and basic knowledge of technical English
• Basic knowledge of office tools (Word, Excel)
• First experience in pharmaceutical production or similar internship
• Knowledge of Good Manufacturing Practices (GMP) or interest in learning
• Experience with document management systems or SAP

Benefits:

• Opportunity to gain valuable professional experience in a real-world setting
• Contribute to improving the health of billions of people
• Certain expenses will be reimbursed

We offer a dynamic work environment where you can develop your skills and acquire valuable experience for your future.

To apply, please visit our website and follow the application process.

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Responsibilities:

• Integrate into a maintenance team and monitor equipment (TGHT, TGBT, backup groups, UPS)
• Participate in and provide support to projects

Requirements:

• Currently pursuing a Bachelor's degree in Electrical Engineering in an alternating education program at a Belgian teaching institution
• Strong interest in maintenance, particularly electrical
• Ability to work in a team
• Adaptability to change and willingness to work following EHS rules
• French language proficiency
• Knowledge of RGIE and electrical distribution is desirable

What's in it for you?

• Opportunity to gain professional experience and develop your skills
• Chance to work with a global biopharma company and contribute to improving public health

How to apply: Interested candidates should apply as soon as possible, as the offer will close once sufficient applications are received.

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As an intern, you will work on real projects and contribute to improving the health of billions of people. You will assist in setting up a robust transition process between production and maintenance periods, streamlining raw material procurement processes, managing projects with operational impact, and participating in the development and follow-up of the production unit's planning.

To be eligible, you must be a student in a European educational institution, fluent in French, and have basic English comprehension. Familiarity with Microsoft Office is required.

The internship is not paid, but certain expenses will be reimbursed according to Belgian law.

Responsibilities:

• Setting up a robust transition process between production and maintenance periods
• Streamlining raw material procurement processes for the production unit
• Managing projects with operational impact
• Participating in the development and follow-up of the production unit's planning
• Improving workflows and available tools within the team
• Acquiring in-depth knowledge of GSK's vaccine supply chain

Requirements:

• Student in Bachelors/Masters in a scientific or industrial field
• Fluent in French, basic English comprehension
• Familiarity with Microsoft Office
• Ability to work as a true business partner and build strong relationships with stakeholders
• Adaptable and able to manage change in a dynamic environment
• Strong communication and collaboration skills
• Curious and motivated by learning and problem-solving

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