Referenznummer: 461605/1 Startdatum: asap Projektdauer: 12 MM Ort: Solothurn
Perform and document daily manufacturing operations in a cGMP environment including operation of process equipment, execution of validation protocols, and revising cGMPdocumentation
Ensure compliance to cGMP as well as maintaining equipment and facilities. The manufacturing associate is detail-oriented with strong understanding of automated systems and processcontrols
Execute manufacturing processing steps and/or manufacturing support activities using electronic batch records
Maintain training to the required level and support other functions on site
Academic background (Life Science, Pharmaceutical, Food, Healthcare or similar)
Minimal to no experience required
We will create a candidate profile containing your strengths and potential and thus increase your chance of being placed in a position
We provide security – attractive salary, punctual payment, full social insurance
Über Hays: With over 15 years of experience in the pharmaceutical industry, biotechnology and medical engineering, we know the key contacts at companies that are recruiting for challenging jobs with real potential. The current high demand for staff has opened up exciting opportunities for dedicated professionals looking to develop themselves professionally and to further their careers. As recruitment specialists with an international network of contacts, we can offer you decisive advantages – all completely free of charge. Register with us and reap the benefits of job offers that are both interesting and relevant to your skills and experience.
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