Technical Process Technology & Validation Intern
GSK Group of Companies
Welcome to Haleon. We're a purpose-driven, world-class consumer company putting everyday health in the hands of millions. In just three years since our launch, we've grown, evolved and are now entering an exciting new chapter - one filled with bold ambitions and enormous opportunity.
Our trusted portfolio of brands - including Sensodyne®, Panadol®, Advil®, Voltaren®, Theraflu®, Otrivin®, and Centrum® - lead in resilient and growing categories. What sets us apart is our unique blend of deep human understanding and trusted science. Now it's time to fully realise the full potential of our business and our people. We do this through our Win as One strategy. It puts our purpose - to deliver better everyday health with humanity - at the heart of everything we do. It unites us, inspires us, and challenges us to be better every day, driven by our agile, performance-focused culture. Please note that only students currently enrolled in a university and able to provide a valid internship agreement will be considered for this position. We are currently looking for a Technical Intern - Process Technology & Validation to join our Nyon site as a key member of the Technical team. You will support the implementation of new technologies and contribute to safe, compliant and robust manufacturing and cleaning processes. Duration: To be confirmed Your Role at Haleon:- You will support the implementation of new technologies for manufacturing and cleaning processes, including digital and modelling solutions.
- You will map and simplify processes, data flows and technical requirements to identify opportunities for standardisation, automation and improved robustness.
- You will support process and cleaning development trials, including preparation, execution, sampling coordination, data collection and interpretation.
- You will contribute to process and cleaning validation activities through risk assessments, scientific rationales, protocols reports and traceable documentation under Technical SME supervision.
- You will analyse manufacturing, cleaning and validation data using appropriate statistical tools and communicate clear conclusions to cross-functional stakeholders.
- You are currently enrolled in or recently graduated from a Master's degree in Engineering, Chemical Engineering, Life Sciences Engineering, Data Science, Computer Science or a related field.
- You have strong analytical thinking and can simplify and structure complex technical problems.
- You are comfortable using Excel and at least one analytical or modelling tool such as Python, MATLAB, R or Minitab.
- You are curious, agile and pragmatic, with an interest in manufacturing, process control, cleaning technologies and validationin a regulated environment.
- You are fluent in written and spoken French and have a good working knowledge of English, with strong communication and collaboration skills.
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