Job Detail

Stellenbeschreibung

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

• Coordinate activities in cooperation with planner and peers


• Acts as SME related to any issue with production equipment


• Analyzes project technical requirements and institutes specific guidelines for the immediate engineering activity


• Prepares summary reports of findings


• Conducts investigations and studies to troubleshoot problems


• Manages relationships externally and internally by supplying industrial manufacturing information as required


• Ensure and document that approved projects are executed and that any changes to media systems and production systems make all required GMP requirements and EHS compliant


• Support the organization to guarantee the technical qualified status according to the current given internal and external requirements supporting the specific qualification owner


• Contributes to standards and guidelines for Quality and EHS


• Participates if necessary in CAPEX project routine meetings


• Ensures site requirements i.e. maintenance, documentation, specifications are considered in CAPEX projects


• Assists as needed in the acceptance of new equipment and the acquisition of documentation


• Reviews and approves the URS document

Qualifikation

Who we are looking for

• University Degree in Engineering or equivalent practical experience


• Technical expertise in the GMP area is a major plus


• In-depth knowledge of quality requirements


• English and German spoken and written


• Analytical thinking for problem solving

This role based in Bern, Switzerland will initially be limited to 12 months with the option of a long term extension. 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!