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Specialist Product Quality // Johnson & Johnson

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27/03/2024 100% Temporary (short-term)
Randstad (Schweiz) AG, c/o Johnson & Johnson
Specialist Product Quality // Johnson & Johnson
Jobdescription

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 Johnson & Johnson 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 120,000 people.

Johnson & Johnson Innovative Medicine is a global pharmaceutical 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:

  • Ensure the GMP-compliant production of active ingredients and drugs for clinical trials and commercial market
  • Contact person for production, development, and quality control for all product quality related topics
  • Ensure that deliverables assigned to Product Quality team as part of projects are successfully achieved on time
  • Review of executed batch records
  • Preparation for batch disposition
  • QA oversight for aseptic processing
  • Review and approval of non-conformities, CAPAs, and Change Controls
  • Ensure the relevancy and effectiveness of corrective and preventive actions
  • Review and approval of SOPs, work instructions and risk assessments
  • LIMS profiles' approval for SEMIs and stability studies
  • SAP Set up for SEMIs
  • Support for internal and external audits as subject matter expert
  • Support complaints management
  • Support for risk management at the site
  • Support the execution of external inspection and audits from local and foreign Health Authorities, including the FDA, and customers
Functie-eisen

Who we are looking for:

  • University degree in pharmacy, natural science, medicine, or equivalent
  • Work experience in a GMP related environment, preferable in Quality is a major plus
  • Good communication skills in English language
  • Communication skills in German is a plus
  • Excellent communication and teamwork skills
  • Ability to work in a diverse and changing environment
  • Ability to prioritize and to continuously review priorities

This job based in Bern, Switzerland will initially be limited to 12 months. If you are interested in working with a global leading pharmaceutical company in a dynamic, inclusive and collaborative environment, then send us your application today. Or give us a call if you have any questions!

Stephan Zoebeli

Address

Randstad (Schweiz) AG, c/o Johnson & Johnson


About the company
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