Job type: Full-time

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“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.

For our site in Bern we are looking for a highly committed

Sr Associate Scientist QC Release & Stability (f/m/d)

Purpose of the Position

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, Capillary Western analysis, ELISA, WES, gel based methods, qPCR, RP-HPLC, SEC and Ion chromatography.

Tasks
  • Be compliant with general guidelines, procedures and processes in the QC in accordance with the internal rules. This includes all steps of the analysis under cGMP from the sample collection point to the release of the results by the authorized person.
  • Timely and effective completion of lab events, investigations and CAPA including writing, execution and review of related documents
  • Maintenance, care and GMP-compliant handling of the devices and technical aids used in the QC.
  • Writing scientifically sound technical documents and reports
  • Perform laboratory duties to support department objectives
  • Periodic review and evaluation of analytical assays (cGMP) according to given timelines if needed
  • Support in planning activities if needed
  • Performing of qualification, verification and co-validation activities
  • Analyzing and reporting test results
  • Drive continuous improvement projects within Quality Control in operational efficiency and GMP compliance

Qualifications
  • Master or PhD in Chemistry, Biochemistry or a related field with an analytical background
  • 1 - 3 years of professional experience in Pharma, Biotech or Vaccines industry is a major plus
  • Hands-on experience with biochemical or chemical technologies and bioassays
  • GMP knowledge
  • 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
  • Analytical thinking and problem-solving skills
  • Ability to work in a dynamic environment (separate bullet point)
  • Your team spirit allows you to integrate easily into an existing team
  • Good level of spoken and written German and English (separate bullet point)
  • Ability to simultaneously manage multiple projects, duties and assignments and prioritize accordingly

Primary Location

Switzerland-Berne-Bern-

Organization

Janssen Vaccines AG (8851)

Job Function

R&D

Requisition ID

2105987442W

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Deadline: 02-05-2024

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