Stability Coordinator, Drug Product Services
vor 5 Tg.

At Lonza, we invest in great people. We encourage our employees to challenge themselves and we offer an environment that fosters creativity and success.

Headquartered in Basel, Switzerland, we operate production, R&D, and business sites around the world, including Europe, North America, and Asia.

Our vision :

We strive to be the leading supplier using science and technology to improve the quality of life.

Our mission :

We work with passion, using advanced technologies, to transform life science into new possibilities for our customers.

Do you want to help us as we shape the future of this great organization?

Job Description Summary

For DPS (Drug Product Services) in Basel Switzerland, we have an open position for a Stability Coordinator in our growing team.

Working closely with Analytical and Formulation Development, this team offers specialized services solutions for customers.

Become part of this exciting opportunity by applying for the position of Stability Coordinator, DPS.

Key Responsibilities :

  • Carry out supporting activities on all DPS stability programs according to current regulations (e.g. cGMPs), including : -
  • physical setup of stability studies (staging) according to relevant stability protocol, updating and maintaining stability planning / scheduling tools and LIMS according to relevant stability protocols, ensuring timely execution of tests in-

    house or at partner sites according to the respective protocols, close coordination with the DPS Lab Manager and people responsible for lab planning and scheduling

  • Manage logistics of pharmaceutical samples according to internal procedures (e.g. good receipt and shipments)
  • Authors required documents in support of GMP stability programs.
  • Generates metrics for stability programs.
  • Supports regulatory inspections as the subject matter expert for stability studies. Perform other duties as assigned.
  • Required Qualifications and Skills

  • A degree in Life Sciences such as Analytical Chemistry, Biochemistry, Pharmacy or related
  • Excellent working knowledge and solid experience working in a GMP environment.
  • Good working knowledge in stability testing of pharmaceuticals.
  • Experience and understanding of ICH stability guidelines.
  • Prior experience with QC stability and sample management and LIMS.
  • Good working knowledge in biotechnology development processes
  • Excellent communication skills
  • Excellent reporting and scientific skills
  • Ability to work independently and in a team environment
  • Strong attention to detail and well structured
  • Good inter-personal skills
  • Enthusiastic and open-minded
  • Willingness to learn and carry out new and complex tasks
  • Proactive attitude
  • Excellent knowledge of written and spoken English
  • Basic knowledge of spoken German
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