Specialist Product Quality // Johnson & Johnson

☞ Randstad Switzerland

View: 151

Update day: 24-04-2024

Location: Bern Bern BE

Category: Quality Assurance / Quality Control

Industry: Staffing Recruiting Biotechnology Research Pharmaceutical Manufacturing

Position: Entry level

Job type: Full-time

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Job content

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 135,000 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. The Bern site, with its approx. 500 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
  • Review of executed batch records
  • Preparation for batch disposition
  • Ensure the quality of produced materials
  • QA oversight for aseptic processing
  • Review and approval of documents, e.g. SOPs, work instructions and risk assessments, master batch records
  • Ensure the GMP-compliant production of active ingredients and drugs for clinical trials and marketed product
  • Ensure that deliverables assigned to Product Quality team as part of projects are successfully achieved on time
  • Contact person for production, development, and quality control for product quality related topics
  • Support Quality Operations and QA LMM in ensuring GMP readiness for NPI projects
  • Support review and release of batches of purchased raw materials and their qualification
  • Support the achievement of KPIs
  • Support the execution of external inspection and audits from local and foreign Health Authorities, including the FDA, and customers
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
  • Flexibility, accuracy and reliability
  • Ability to prioritize and to continuously review priorities
This job based in Bern, Switzerland will initially be limited to approx. 12 months. 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 #50plus
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Deadline: 08-06-2024

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