- QA Release of excipients and other direct materials
- Evaluation and assessment of change records
- Review and approval of relevant GMP-documents
- OOS, deviation management and CAPA review and approval
- Review and approval of risk assessments in the area of responsibility
- Collaboration with our interfaces to Quality Control (QC) personnel and other departments to ensure a constant state of inspection readiness by identifying, escalating and working to resolve compliance risks in the area
- Master degree or PhD in Life Sciences and preferably severeal years of relevant experience in the pharmaceutical industry
- Demonstrated experience in quality assurance (and additionally preferably quality control)
- Knowledge of cGMP and Quality requirements
- Results-oriented, analytical working style
- Agile mindset, that is characterized by embracing change and the ability to work in self-organizing teams
- Ability to communicate clearly and professionally both verbally and in writing in German (C2) as well as English (C1)
- You will work in an international environment
- A very renowned company
Ihr Kontakt
Referenznummer
801110/1
Kontakt aufnehmen
Telefon:+41 44 225 50 00
E-Mail: positionen@hays.ch
Anstellungsart
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With over 15 years of experience in the pharmaceutical and chemical industry as well as in 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 experts who want to develop professionally and to further their careers. As recruitment specialists with an international network of contacts, we can offer you decisive advantages – completely free of charge. Register with us and reap the benefits of interesting job offers that match your skills and experience.
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