Position: Entry level

Job type: Full-time

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Job content

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 265 operating companies in more than 60 countries employing approximately 135,000 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, with its approx. 500 people of over 25 nationalities, acts as a center of expertise for development and manufacturing of innovative cell based viral- and bacterial vaccines and bacterial based therapeutic products.

Main Responsibilities
  • Support the qualification and validation activities of computerized and non-computerized systems within the Quality Control department
  • Perform and/or support the writing of specification documents (URS) & system impact assessments (SIA)
  • Support the calibration & maintenance of laboratory equipment
  • Review test protocols, plans and reports
  • Support test execution
  • Supporting the timely and effective completion of investigations, change controls and CAPA’s
Who We Are Looking For
  • Degree in a LifeSciences/Biotechnology, Chemistry discipline or comparable work experience
  • Experience with the use and qualification of laboratory and analytical QC equipment
  • Good understanding of analytical technologies
  • Strong analytical thinking and problem-solving ability
  • Excellent communication and teamwork skills
  • Ability to simultaneously support multiple projects, duties and assignments and prioritize accordingly
  • Excellent writing skills for scientifically sound technical documents, instructions, protocols and reports
  • Self-dependent way of working and taking ownership of assigned task to plan and deliver according to agreed timelines
  • Good verbal and written skills in English, German is a plus
This job based in Bern, Switzerland will initially be limited to approx. 12 months. If you are interested in working with a global leading pharmaceutical company in a dynamic, progressive, and collaborative environment, then send us your application today. Or give us a call if you have any questions!

#diversity #50plus
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Deadline: 09-06-2024

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