Validation Specialist // Johnson & Johnson in Bern

veröffentlicht
Kontakt
Stephan Zoebeli, Randstad JnJ HQ
Jobtyp
Temporär
jetzt bewerben

job details

veröffentlicht
Ort
Bern
Sektor
Bau
Jobtyp
Temporär
Referenznummer
127140-72
Kontakt
Stephan Zoebeli, Randstad JnJ HQ
Telefon
058 231 57 94
jetzt bewerben

Stellenbeschreibung

Caring for the world, one person at a time... inspires and unites the people of Johnson & Johnson. 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 230 operating companies in more than 60 countries employing approximately 126,400 people. Our worldwide headquarters is in New Brunswick, New Jersey, USA.


Janssen Vaccines AG, 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.


Main Responsibilities:


The Validation Specialist is accountable for delivering compliant controlling and manufacturing systems including utilities to the users by reviewing and approving qualification / validation documentations. Also, he/she will pro-actively valuable inputs regarding cost saving and EHS to direct line responsible. He/she will also support process documents periodic review and improvements. Key tasks will include but are not limited to:



  • Review / approval of qualification documents in accordance with local, global standards and regulations

  • Review / approval of validation documents in accordance with local, global standards and regulations

  • Writing / reviewing process documents (procedure, instruction)

Qualifikation


  • Bachelor degree in Sciences, Applied Sciences or Quality

  • Knowledge in cGMP processes is a major plus

  • Knowledge of systems / utilities qualification is a plus

  • Analytical thinking and problem-solving ability

  • Strong communication ability

  • English, written and spoken, German appreciated

  • Time and self-management

  • Basic software skills (Windows pack)

This role based in Bern, Switzerland will initially be limited to approx. 6 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!