Associate Scientist QC Analytics // Johnson & Johnson in Bern

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

job details

veröffentlicht
Ort
Bern
Sektor
Life Sciences
Jobtyp
Temporary
Referenznummer
127140-123
Kontakt
Stephan Zoebeli, Randstad Inhouse Services J&J Zug
Telefon
058 231 57 94
jetzt bewerben

Stellenbeschreibung

'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 134,000 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 30,000 professionals working passionately to prevent, treat, cure and stop some of the most devastating and complex diseases of our time. In Bern, about 300 people of over 20 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 bring meaningful innovation to global health by combating major threats to the health of people worldwide.

Main Responsibilities

After the respective trainings, you are expected to coordinate and conduct analytical testing on raw products, raw materials and various other samples. The analytical methods applied in-house range from Western Blot, ELISA, gel based methods, RP-HPLC, SEC- and Ion chromatography.

  • Responsible for performing various release, stability, IPC and raw material testing according to internal and/or regulatory (EP, USP, ISO, other) standards for QC testing
  • Write scientifically sound technical documents and reports
  • Responsible for 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

  • University/Higher educational degree in LifeScience discipline with microbial and/or analytical background
  • Work experience in Pharma, Biotech or Vaccines industry is a major plus
  • GMP experience is a plus
  • Experience in method validations and verifications 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
  • Business fluent in German
  • Good English communication (verbal & written)

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