Scientist QC Analytics // Johnson & Johnson in Bern

veröffentlicht
Kontakt
Stephan Zoebeli, Randstad Inhouse Services J&J Zug
Jobtyp
Temporär
jetzt bewerben

job details

veröffentlicht
Ort
Bern
Sektor
Life Sciences
Jobtyp
Temporär
Referenznummer
127140-176
Kontakt
Stephan Zoebeli, Randstad Inhouse Services J&J Zug
Telefon
058 231 57 94

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:

The QC department is involved in the validation and transfer of various test methods as well as in performing of routine release and stability tests for novel clinical phase materials. The analytical methods applied in-house range from Western Blot, ELISA, WES, gel-based methods, RP-HPLC, SEC- and Ion chromatography. The scope of this temporary Scientist position is to support the QC team in the following areas:

  • Performing of qualification, verification and co-validation activities
  • Performing of product release, stability and IPC testing
  • Analyzing and reporting test results
  • Writing scientifically sound technical documents and reports
  • Maintenance of laboratory equipment and operation of analytical and other instruments
  • Drive continuous improvement projects within Quality Control in operational efficiency and GMP compliance
  • Timely and effective completion of lab events, investigations and CAPA including writing, execution and review of related documents

Qualifikation

Who we are looking for:

  • PhD in Chemistry, Biochemistry or a related field with an analytical background
  • Professional experience in Pharma, Biotech or Vaccines industry is a major plus
  • Hands-on experience with analytical technologies and bioassays (e.g. HPLC, IC, GC, IEF, SDS-PAGE, ELISA)
  • GMP knowledge is a major plus
  • Demonstrate innovative spirit, strong interpersonal skills and project management abilities
  • Independent way of working and taking ownership of assigned tasks, planned individually and delivered according to agreed timelines
  • Ability to simultaneously manage multiple projects, duties and assignments and prioritize accordingly
  • Your team spirit allows you to integrate easily into an existing team
  • Good level of spoken and written German and English

This role based in Bern, Switzerland will initially be limited to 12 months. If you are interested in working for a globally 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!