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QC analyst I (CDD 1 an)

Neuchâtel, Switzerland


Every day, employees working in Takeda’s Global Manufacturing and Supply Chain, and Global Quality business unit are shaping the future of healthcare. They are breaking down barriers and ensuring our life-changing medicines are available, accessible, and affordable to patients. Life-changing for you. Life-changing for patients.

Global Manufacturing and Supply Chain, and Global Quality is the backbone of Takeda, and our employees are the guardians for our patients, our products, and our reputation. As a member of our team, we can offer you the opportunity to grow in a meaningful career, develop your skills, and come to work every day knowing that what you do makes a genuine difference.

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What makes a successful member of our team? Check out the traits we’re looking for and see if you have the right mix.

  • Agile
  • Ambitious
  • Analytical
  • Collaborative
  • Enthusiastic
  • Entrepreneurial

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  • Bold initiatives, continuous improvement, and creativity are at the heart of how we bring scientific breakthroughs from the lab to patients.

  • Here, you will feel welcomed, respected, and valued as a vital contributor our global team.

  • Through trust and respect, you will have genuine support from leaders, managers, and colleagues to do your best work.

  • A strong, borderless team, we strive together towards our priorities and inspiring mission.

  • Recognized for our culture and way of working, we’re one of only 13 companies to receive Top Global Employer® status for 2018.

  • Our people-first mission extends beyond patients to include their families, communities, and our own Takeda family.

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QC analyst I (CDD 1 an)

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Job ID SR0042843 Date posted 10/29/2019 Location Neuchâtel, Switzerland


Rattaché(e) au département « Quality Control – Analytical Laboratory  ».

L’horaire s’appliquant à ce poste de travail est l’horaire de journée (variable)

Votre mission

La mission principale du département « Quality Control – Analytical Laboratory » est de réaliser les analyses physico-chimiques et biochimiques nécessaires pour déterminer la qualité et la stabilité des produits en cours de fabrication et des produits finis.

Responsabilités principales

  • Effectuer les analyses des matières premières selon les pharmacopées et selon les procédures opérationnelles et protocoles définis, dans le respect des plannings et des délais, en accord avec les bonnes pratiques de laboratoire
  • Supporter l’investigation en cas de résultats invalides si nécessaire
  • Préparation de solutions et tampons
  • Participer au maintien et à l’amélioration continue des processus du laboratoire
  • Participer au bon fonctionnement du laboratoire, dans le respect des standards 5S et EHS

Profil recherché

  • Idéalement 2 ans d’expérience dans l’industrie pharmaceutique. Titulaire au minimum d’un CFC de laborantin/e ou équivalent dans le domaine technique de la biologie, biochimie ou dans un domaine proche
  • Application des règles de Bonnes Pratiques de Fabrication (cGMP) et d’Eudralex
  • Connaissance, interprétation et application des pharmacopées (Européennes, Japonaises, Américaines)
  • Bonne communication verbale et écrite en français, l’anglais représente un atout
  • Méthode et rigueur dans le travail avec une facilité d’analyse de problèmes techniques
  • Disponibilité et flexibilité avec un fort esprit d’équipe
  • Caractère dynamique et volontaire

Notice to Employment / Recruitment Agents:

Employment / Recruitment agents may only submit candidates for vacancies only if they have written authorization to do so from Shire, a wholly-owned subsidiary of Takeda’s Talent Acquisition department. Any agency candidate submission may only be submitted to positions opened to the agency through the specific Agency Portal. Shire, a wholly-owned subsidiary of Takeda will only pay a fee for candidates submitted or presented where there is a fully executed contract in place between the Employment / Recruitment agents and Shire, a wholly-owned subsidiary of Takeda and only if the candidate is submitted via the Agency Portal. Candidates submitted or presented by Employment / Recruitment Agents without a fully executed contract or submitted through this site shall not be deemed to form part of any Engagement for which the Agency may claim remuneration.

Job ID SR0042843

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