(Senior) QA Specialist (f/m/d)

Lonza AG

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  • Date de publication :

    12 février 2024
  • Taux d'activité :

    100%
  • Type de contrat :

    Durée indéterminée
  • Lieu de travail :

    Visp

(Senior) QA Specialist (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 a (Senior) QA Specialist who will support to establish and maintain quality management & compliance processes at Visp site. The QA Specialist will be responsible to provide QA support in the Bioconjugates Business Unit. You will work closely with various quality and operational functions to ensure GMP-compliant manufacturing and documentation.

Key responsibilities:

  • Responsible for project specific QA Operation work during commissioning/qualification 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 multi-product, GxP contract manufacturing facility

  • Review GMP records to ensure compliance with cGMP per written procedures (e.g., batch records, TW records, etc)

  • 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's degree within the field of natural sciences or related

  • Working experience from QA Operations in the Biopharma environment

  • Knowledge and experience of the practical and theoretical requirements of quality management system in a GMP facility

  • Hands-on experience coordinating & interacting with internal departments on manufacturing activities

  • Fluent in English, German is preferred

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: R58676

Contact

  • Lonza AG

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