水平: Entry level

工作类型: Full-time

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工作内容

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 135,000 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 40,000 professionals working passionately to prevent, treat, cure and stop some of the most devastating and complex diseases of our time. In Bern, about 400 people of over 25 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.

For our USP Development team we are looking for an open-minded, motivated team player with a background in microbial or mammalian cell fermentation. As part of the USP Development team you will be involved in characterization and development activities of API manufacturing processes from shake flask to 10L bench scale system.

Main Responsibilities
  • Achieve cost efficient API manufacturing processes through optimization, characterization, scale-up and validation work and provision of the required compilation according to GLP
  • Document and present study reports
  • Plan, write and execute studies for development activities utilizing advanced skills in QbD, DoE and data analysis to drive characterization studies and CMC enabling documentation
  • Evaluation of data using state of the art statistical tools
  • Review and create GLP documentation (equipment instructions, work instructions)
  • Work towards the identification, assessment and development of new scientific concepts and technologies
  • Supports continuous improvements in the development of new refined materials, processes, products and/or scientific procedures
  • Support GMP activities during clinical trial manufacturing at pilot scale in a GMP environment
  • Participate in regular lab inspections to ensure safety at work
Who We Are Looking For
  • MSc level studies in Biotechnology / Biology / Chemistry or equivalent
  • Work experience with microbial or mammalian cell cultivation is a plus
  • Background in statistics is advantageous
  • Good level of communication in German and English
  • Passionate team player and communicative personality
This job is based in Bern, Switzerland and will initially be limited to 12 months. If you are interested in working for a global leading health care company, in a highly dynamic and flexible work environment, then send us your application today. Or give us a call if you have any questions!

#diversity #50plus
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最后期限: 10-05-2024

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