Position title
Global Quality Systems Data Scientist Specialist
Description

 

Today, Lonza is a global leader in life sciences operating across three continents. While we work in science, there’s no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that’s the kind of work we want to be part of.

We are looking for an agile person to join our Global QMS team. The Global Quality Systems Data Scientist Specialist will support initiatives for the global QMS-DMS team at Global level in the implementation of new advanced digital technologies enabling more efficient and effective ways of working as well as increasing automation and simplification of quality related activities. As part of the Global QMS team you would act as the global coordinator for our document management system assisting system users and managing system master data.

Key responsibilities:

  • Actively participate in the implementation of systems, tools and processes related to data management, data modeling and reporting.
  • Support the Global QMS -DMS Team with development and maintenance of existing reporting and monitoring tools (dashboards, databases, and KPI’s) leveraging Microsoft Power BI and Excel.
  • Perform data analysis by utilizing relevant tools (e.g., SQL).
  • Act as Global Super User/Coordinator of DMS application
  • Act as point of contact for resolution of Global DMS user support requests (incl. F11 ticketing and email requests).
  • Support on the approval of specific global documentation (last approval role)
  • Support the Global QMS-DMS team to implement DMS improvements and in the management of technical issues and testing

Key requirements:

  • Degree in technical fields like Biochemistry, Chemistry, Pharmaceutical Sciences, Computer Science, or Engineering.
  • At least 3 years of experience with Quality System management in a GMP regulated environment
  • At least 3 years of experience in the (Bio)pharmaceuticals or similar highly regulated  industry
  • Solution drive
  • Very strong PC and Software skills and excellent knowledge in Data management and data tools (SQL)
  • Experience and/or good understanding of Processes Mapping and Process performance is a plus
  • Solution drive
  • Is enthusiastic and actively contributes to discussions aimed at the continuous improvement of the QMS
  • Ability to communicate and efficiently / effectively  interact in an international environment
  • Good knowledge of English (written and spoken), German is a plus

Every day, Lonza’s products and services have a positive impact on millions of people. For us, this is not only a great privilege, but also a great responsibility. How we achieve our business results is just as important as the achievements themselves. At Lonza, we respect and protect our people and our environment. Any success we achieve is no success at all if not achieved ethically.

People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences. In return, we offer the satisfaction that comes with improving lives all around the world. The satisfaction that comes with making a meaningful difference.

How the process will look like

Your teammates will gather all requirements within our organization. Then, once priority has been discussed, you will decide as a team on the best solutions and architecture to meet these needs. In continuous increments and continuous communication between the team and stakeholders, you’re part of making data play an even more important (and understood) part withing Brand New Day.

 

Job Benefits

EUR 92K - 170K *

Employment Type
Full-time
Beginning of employment
asap
Job Location
CH - Basel HR
Working Hours
40
Base Salary
euro EUR 92K - 170K *
Date posted
June 6, 2024
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