Biotechnologist Drug Product Ibex® (m/w/d)

☞ CH12 Lonza AG

View: 163

Update day: 01-04-2024

Location: Visp Valais VS

Category: R & D IT - Software

Industry: Human Resources Services

Position: Mid-Senior level

Job type: Full-time

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Job content

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.Ibex® Solutions (www.ibex.lonza.com) is a modular build complex to develop and manufacture biological products. It enables companies to get access to a complete solution, gaining speed and achieving a simplified value chain.The Ibex® Complex is our contribution to the medicine of tomorrow and possibly the next step in your career?At our location in Visp, in the canton of Valais, we are constantly looking for Biotechnologists with a relevant background at all levels in Life Sciences in order to support our growth in several business units.Key Responsibilities
  • Executes manufacturing activities in the area of Drug Product according to cGMP guidelines, ensuring batch execution, evaluating test results, resolving issues, troubleshoot manufacturing equipment and make recommendations for resolution.
  • Provides front line technical and procedural support, working with the manufacturing team.
  • Securing each batch is manufactured safely, on time, in compliance with the batch instructions and quality requirements
  • Responsible to establish timely and with high quality the required production documentation (preparation, execution and review of batch records) or other relevant GMP documents for the assigned production area.
  • Supports process related investigations and assists in decision making on production issues
  • Supports process changes and CAPAs related to processes within required timelines
  • Performs training activities of relevant areas as operator and supports others and new joiners.
Key Requirements
  • 1-3 years of experience GMP environment on the shopfloor (preferably in sterile manufacturing of Drug Product)
  • Fluent in either English or German
  • Familiar with GMP requirements, quality procedures and SOP execution
  • Strong team orientation
  • Good communication skills and interaction with a variety of interfaces within the organization
  • Structured, focused and well-organized working attitude
  • High motivation and dynamic drive
  • IT knowledge and knowledge in SAP and MES is a benefit
  • Prepared to work flexible working hours
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.
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Deadline: 16-05-2024

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