Roche develops medicines and diagnostic solutions. Its Swiss activities include research and development and pharmaceutical and diagnostics work, notably in Basel, Kaiseraugst and Rotkreuz.
Internship Process Engineer (for 12 months in Basel)
Cet internship de Process Engineer chez Roche Suisse, au sein de la fabrication de substances pharmaceutiques à Bâle, porte sur la validation des procédés et les transferts de technologie. Vous contribuerez notamment aux livrables de validation, à l'interprétation des données, au traitement des déviations selon les normes GMP et aux projets d'optimisation. Le stage dure 12 mois et requiert un cursus scientifique ou technique ainsi que l'anglais courant ; l'allemand conversationnel est un atout.
Information about Roche Suisse
- Official domain
- roche.com
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Job details
The full description published by Roche Suisse.
Description de l’offre
Chez Roche, vous pouvez être vous-même et être apprécié pour les qualités uniques que vous apportez. Notre culture encourage l'expression personnelle, le dialogue ouvert et les connexions authentiques, où vous êtes valorisé, accepté et respecté pour ce que vous êtes, vous permettant de prospérer tant personnellement que professionnellement. Voici comment nous visons à prévenir, arrêter et guérir les maladies et à garantir à chacun l'accès aux soins de santé aujourd'hui et pour les générations à venir. Rejoignez Roche, où chaque voix compte.
La position The Process Validation Chapter is a part of the Basel Drug Substance Manufacturing organization and is responsible for supporting the validation of the production process during routine commercial manufacturing, technology transfers, process optimizations and for leading implementation of new technologies to drive manufacturing efficiencies. This internship position is located in Basel, Switzerland. The Opportunity:
- You will contribute to process validation strategies, execution, and projects to drive operational success across manufacturing.
- Supporting technical process technology transfers enables you to play a key role in transitioning processes from development into commercial-scale manufacturing.
- You will manage end-to-end validation deliverables, spanning conceptual work, plan creation, training implementation, sample coordination, data interpretation, and report preparation.
- Cross-functional troubleshooting activities will be planned and coordinated by you in close collaboration with pilot laboratories, production, and the quality department.
- You will process deviations and changes in full compliance with GMP guidelines.
- Active involvement in optimization projects will allow you to drive continuous improvement, efficiency, and process robustness. Who You Are:
- You are currently enrolled in a Bachelor’s or Master’s program, or have completed your degree within the last 12 months prior to the start date, in a scientific or technical field—preferably in Biotechnology, Bioprocess engineering, or (bio)Chemical engineering, Pharmacy, Biology.
- Practical experience or solid knowledge of working within a regulated GMP environment will be a core foundation of your qualifications.
- You will bring a collaborative mindset as an independent team player who thrives in a dynamic environment and enjoys partnering across diverse interfaces.
- Adapting quickly to a fast-paced setting will enable you to manage shifting priorities effectively and respond with agility to operational requests.
- Strong interpersonal and communication skills will allow you to articulate complex technical topics clearly and build productive working relationships.
- Fluency in English is required to collaborate and communicate clearly within an international, cross-functional team. Conversational German skills are considered an asset.
Additional Information
- Start : Date &
- Duration : The preferred
- start : date for the internship is in early 2027 with a
- duration : of 12 months (or upon mutual agreement).
Application Process
- Please upload your CV (in English), a motivation letter with your application, and a certificate of enrollment (if you are currently studying) or your degree certificate (if you have already completed your studies). - Non-EU/Non-EFTA citizens must attach an official confirmation from your university stating that a mandatory internship is an integral part of your curriculum, and you must remain continuously enrolled throughout the entire duration of this internship. Ready to take the next step? We look forward to receiving your application!
Qui nous sommes Un avenir plus sain nous pousse à innover. Ensemble, plus de 100 000 employés à travers le monde sont dédiés à faire progresser la science et à garantir à chacun l'accès aux soins de santé aujourd'hui et pour les générations à venir. Nos efforts aboutissent à plus de 26 millions de personnes traitées avec nos médicaments et plus de 30 milliards de tests réalisés avec nos produits de Diagnostique.
Nous nous encourageons mutuellement à explorer de nouvelles possibilités, à favoriser la créativité et à conserver nos grandes ambitions, afin de fournir des solutions de santé qui changent des vies et ont un impact mondial. Construisons ensemble un avenir plus sain. Roche est un employeur offrant l'équité en matière d'emploi.
Requirements
- Bachelor’s ou Master’s en domaine scientifique ou technique
- Expérience pratique ou connaissances solides d’un environnement GMP réglementé
- Esprit collaboratif
- Capacités interpersonnelles et de communication
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