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Operator/Biotechnologist (m/f/d).

Job Details

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Job Details

We are looking for a Biotechnologist (m/f/d) for Lonza AG (100%). This is a temporary position for 3 months, with an opportunity to extend.

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

Key responsibilities

  • Manual visual inspection of liquid and lyophilized vials

  • Defect classification according to regulations

  • Periodic qualification and requalification using existing test sets

  • Assistance in the creation of new test sets and their annual qualification

  • Support in case of deviations and clarification of root causes

  • Sample collection after visual inspection

  • Focal points of the tasks:

  • GMP-compliant work and timely documentation of the work performed (e.g. computer systems (MES) or logs).

  • Ensure correct execution of processes/procedures

  • Know the process flows

  • Recognize potential problem at an early stage and report it

  • Assisting with the induction of new employees

  • Know the relevant SOPs and regulations (e.g. hygiene concept, safety regulations, etc.) and complies with them.


We are looking for a Biotechnologist (m/f/d) for Lonza AG (100%). This is a temporary position for 3 months, with an opportunity to extend.

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

Key responsibilities

  • Manual visual inspection of liquid and lyophilized vials

  • Defect classification according to regulations

  • Periodic qualification and requalification using existing test sets

  • Assistance in the creation of new test sets and their annual qualification

  • Support in case of deviations and clarification of root causes

  • Sample collection after visual inspection

  • Focal points of the tasks:

  • GMP-compliant work and timely documentation of the work performed (e.g. computer systems (MES) or logs).

  • Ensure correct execution of processes/procedures

  • Know the process flows

  • Recognize potential problem at an early stage and report it

  • Assisting with the induction of new employees

  • Know the relevant SOPs and regulations (e.g. hygiene concept, safety regulations, etc.) and complies with them.


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MS

Mari Slavova

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