Specialist QC Services // Johnson & Johnson in Bern

Stephan Zoebeli, Randstad Inhouse Services Johnson&Johnson Zug
jetzt bewerben

job details

Life Sciences
Stephan Zoebeli, Randstad Inhouse Services Johnson&Johnson Zug
058 231 57 94


Caring for the world … one person at a time inspires and unites the people of Johnson & Johnson. This culture of caring is the focus of our corporate philosophy, that is anchored in the internationally applicable Credo. We embrace research and science - bringing innovative ideas, products and services to advance the health and well-being of people. Employees of the Johnson & Johnson Family of Companies work with partners in health care to touch the lives of over a billion people every day, throughout the world. We have more than 260 operating companies in more than 60 countries employing approximately 134,000 people. Our worldwide headquarters is in New Brunswick, New Jersey, USA.

Janssen Vaccines in Bern (Switzerland) belongs to the Janssen Pharmaceutical Companies of Johnson & Johnson. Janssen is an organization of over 30,000 professionals working passionately to prevent, treat, cure and stop some of the most devastating and complex diseases of our time. In Bern, about 300 people of over 20 nationalities work together with the wider Janssen organization and partners on the development, manufacturing and analytical testing of novel vaccines and bacteria-based pharmaceutical products. We are committed to bringing meaningful innovation to global health by combating major threats to the health of people worldwide.

Main Responsibilities

  • Managing outsourcing activities (Organization of sample shipments and analytical testing with internal and external partners (CROs, other J&J sites))
  • Coordinating equipment maintenance activities with QC laboratories, external suppliers, quality and Technical Services
  • Supporting equipment/system qualification and validation activities within the QC department (e.g. clarification with vendors and the QC testing labs, ordering equipment, writing technical documents)
  • Supporting the timely and effective completion of investigations, change controls and CAPA's related to sample shipment and equipment activities
  • Driving continuous improvement projects within the Quality Control Department in operational efficiency and GMP compliance
  • Helping to build a strong team to expand, strengthen and maintain the current knowledge base and expertise within QC to reflect changing business needs


Who we are looking for

  • University degree
  • Excellent communication skills in English, German is a plus
  • Good organization and teamwork skills
  • Strong analytical thinking and attention to detail
  • Strong work experience with IT systems (advanced Excel, Sharepoint, LIMS, SAP or similar)
  • Ability to simultaneously support multiple projects, duties and assignments and prioritize accordingly
  • Independent way of working and taking ownership of assigned task to plan and deliver according to agreed timelines
  • Good understanding of analytical technologies and GMP experience is a plus

This role based in Bern, Switzerland will initially be limited to approx. 12 months. If you are interested in working for a global leading health care company in a challenging role, then send us your application in English today. Or give us a call if you have any questions!