Validation Specialist // Johnson & Johnson in Bern

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

job details

Stephan Zoebeli, Randstad Inhouse Services J&J Zug
058 231 57 94
jetzt bewerben


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 130,000 people. Our worldwide headquarters is in New Brunswick, New Jersey, USA.

Janssen Vaccines, one of the Janssen Pharmaceutical Companies of Johnson & Johnson, is a global biopharmaceutical company dedicated to bringing meaningful innovation to global health. We do this by discovering, developing, manufacturing and marketing products that combat major threats to the health of people worldwide. The Bern site acts as a center of expertise for development and manufacturing of innovative cell based viral- and bacterial vaccines and is recently expanding its portfolio into bacterial based therapeutic products.

Main Responsibilities

  • Accountable for delivering compliant controlling and manufacturing systems and processes to the users by leading adequate qualification / validation activities with additional focuses on EHS, cost reduction and project timelines
  • Support on time closure on maintenance / calibrations / notifications task within SAP
  • Support operational document compliance
  • As project member, support Quality status overview (GMP Readiness) on systems
  • Support investigation / corrective and preventive actions as Quality Leader
  • Report and maintain KPIs for SAP Quality tasks
  • Proactively solves and / or communicate challenges in timely manner to support Quality and site objectives
  • Ensure Validation process compliance with regulations and standards
  • Ensure timely review/approval of operating documents / Validation documents and, appropriate alignment within Quality Operations (e.g. alignment with qualification by reviewing an equipment job instruction)


Who we are looking for

  • University degree in a Life Sciences or Engineering discipline
  • Knowledge in cGMP processes is a major plus
  • Knowledge in biological manufacturing processes is a major plus
  • Excellent problem solving and analytical capabilities
  • Team player and a personality with excellent interpersonal communication skills
  • Capacity to communicate fluently in English and preferably German

This role based in Bern, Switzerland will initially be limited to approx. March 2020. 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!