Senior QA Specialist Vibe-X (f/m/d)

Lonza AG

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  • Publication date:

    29 February 2024
  • Workload:

    100%
  • Contract type:

    Unlimited employment
  • Place of work:

    Visp

Senior QA Specialist Vibe-X (f/m/d)

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.

Currently we are looking for Senior QA Specialists, who will work on our new growth project Vibe-X. As a member of a CAPEX projects Quality Project team, you will manage the QA related activities in close contact with QC, Engineering and Manufacturing to ensure the quality oversight is given. You will ensure timely delivery of project, even in the face of project requirements and priorities through excellent planning and management of the project.

Join Lonza and apply for this innovative opportunity!

Key responsibilities:

  • Responsible for project specific QA Operation work during commissioning/qualification and project tech transfer in IBEX

  • Assess and manage tasks that would impact Quality operation during GMP manufacturing

  • Plan for future activities and coordinate with other departments (e.g. QC, Engineering, Manufacturing) to complete the planned activities

  • Support day-to-day Quality Assurance activities in accordance with approved SOPs/Policies for a GMP manufacturing facility

  • Review GMP records to ensure compliance with cGMP per written procedures

  • Make real-time decisions on process events on the floor, based on knowledge of defined SOPs & policies

  • Participate in walkthroughs and audit/inspections

Key requirements:

  • Bachelor of Science in Life Science or a related field

  • Significant experience in the pharmaceutical quality area

  • Work experience in a role in Quality Assurance, Production or Engineering, in pharmaceutical industries and cGMP controlled environment. QA experience in tech transfer is preferred

  • Excellent knowledge of computer systems (e.g. TW, SAP, etc.) and quality tools such as risk based approaches (e.g. FMEA)

  • Fluency in English

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.

Reference: R59112

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  • Lonza AG

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