Technical Writer // Johnson & Johnson

Administration / Secretarial

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 140,000 people. 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. 600 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 in writing documents for CapEx projects
  • Support in writing and translation (from English to German or vice versa) documents for other Manufacturing Science Drug Substance related projects
  • Providing MSIT Manufacturing Science Drug Substance with document writing support
  • Translation of documents from English to German or vice versa
  • Supports MSIT and GMP Operations to update documentation for WorkInstructions, equipment manuals, repair histories, provide technical data updates, and input necessary changes to e.g. bill of equipment and bill of materials
  • Must be able to work effectively with others at all levels and functional areas on site


Who we are looking for:

  • University degree in pharmacy, natural science, chemistry, medicine or equivalent
  • Working experience as professional technical writer (c)GMP in Quality departments in pharmaceuticals, biotechnologies or chemical industry
  • Kledge of (c)GMP documentation and writing (create, revise, and format new or existing documents (MBRs, SOPs, forms, jobs aids, technical documents, worksheets etc.) and assists in tracking each revision
  • Kledge of GMP-requirements and their technical implementation in cleanrooms and health, work & safety and environment requirements of J&J are an advantage
  • Initiative and team oriented personality with strong communication skills
  • Autonomous working style, very flexible and able to work under pressure
  • SAP kledge in Master data maintenance is a advantage
  • Fluent in English and German

This job based in Bern, Switzerland will initially be limited to approx. 5 months with the opportunity to extend long term. 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 #50 plu