Job description
At LenioBio, we believe every person should have the opportunity to live a healthy and productive life. We have one goal: to simplify manufacturing and speed up drug delivery to the patient. We are in the midst of an incredible journey. Our ALiCE® technology scales with the pharmaceutical R&D process: from discovery to product testing and clinical trials, and finally to GMP-grade production in the form of an end-to-end integrated production platform.
We are looking for passionate individuals who share our mindset of curiosity and commitment to add their knowledge to the team. Do you want to be part of our journey? Then please keep reading.
About this job
We are about to strengthen our manufacturing capabilities for the ALiCE® Production and seek for a motivated team member (all genders) to support our production and research processes.
Your responsibilities: - You will be responsible for collection, cleaning and sterilization of reusable laboratory production items.
- You will provide the cleaned laboratory production items for manufacturing and research activities.
- You will be responsible for cleaning our laboratory equipment in accordance with internal requirements.
- You will be responsible for disposal of all waste produced, taking into account the principles of separation.
- You will support in filling, packaging and labeling of sample solutions including storage.
- You will support in periodic inventory control activities.
- You will record the work carried out in accordance with DIN ISO and/or internal quality documentation.
We are looking for people who want to bring in their best, learn from the best, and create the best. You are an expert in your craft because you love what you do, you know you can become even better, and you are constantly looking for the boundary of the possible.
Requirements
This job will suit you best if you - have worked in laboratory and/or hygiene controlled environments.
- have experience in handling chemicals and hazardous substances within national HSE requirements.
- As a plus: you have experience with QM-conform operations and SOP documentation (cGMP).
- work in a reliable, structured and autonomous manner.
- have level self-initiative and ownership on task that are handed over to you.
- like to work in a team and are fluent in German and English.
- have good knowledge of Microsoft Office tools.
- enjoy learning and increasing your skills on a continuous basis.
A high level of responsibility and care is required for this role. You will have a direct impact on our product quality.
Contact us
Have we aroused your interest? Then we look forward to receiving your application including a cover letter.