Job Detail

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 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, 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:

After the respective trainings, you are expected to coordinate and conduct microbiological and analytical testing on raw materials, products and various other samples.

• Responsible for performing various microbial testing according to internal and/or regulatory (EP, USP, ISO, other) standards for QC testing (sterility, bioburden, endotoxin, growth promotion, etc.)


• Responsible for performing environmental monitoring tests (air and surface sampling; water and gasses sampling etc.) in the QC labs


• Responsible for performing analytical tests on raw materials required for the production process (e.g. FTIR, Ion Identity testing, pH, conductivity)


• Responsible for release and stability testing


• Responsible writing and conducting study plans and method validations work, when the need arises


• Conduct equipment validation and qualification


• Perform laboratory duties to support department objectives


• Supports the Quality department in internal and external audits and requests


• Responsible for compliance with Quality goals for this position


• Provide support to analytical development, process development and other stakeholders when the need arises

Qualifikation

Who we are looking for:

• PhD with relevant work experience


• Work experience in Pharma, Biotech or Vaccines industry is a plus


• Experience in method validation and verification and equipment qualification


• Preferably familiar with compendial testing and related industry guidelines


• Demonstrate innovative spirit, strong interpersonal skills and project management abilities


• Ability to work in a dynamic environment according to tight and challenging timelines


• Team player


• Very Good German & English communication (verbal & written)

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