Quality Assurance Architect
vor 2 Wochen
**My duties**
- Authority
- and customer inspections
- Preparation of GMP documents for regulatory submissions
- Responses to questions from regulators
- Coordination, performance and follow-up of paper based GMP inspections
- Preparation of GMP-certificate renewal and tender relevant documentation based on request by Affiliates
- Change Management: Ensuring timely implementation of Regulatory Compliance related actions
- Supporting answers to Regulatory Compliance related questions from internal or external
- Perform Ad-Hoc duties in specialized field
- Participation in predetermined trainings
- Compliant performance of activities after appropriate training
**My qualifications**
- Education University degree or university of applied sciences degree in natural sciences (e.g. Biology, Chemistry or Pharmacy)
- Experience in Quality or manufacturing in a pharmaceutical GMP environment
- Experienced in reading regulations
- Demonstrated german and english skills (written and spoken)
- Demonstrated communication skills
- Demonstrated interest for technical processes
**My benefits**
- A very renowned company
- Modern company spirit and modern working environment
- Good chances of a permanent position
- A highly motivated team and an open way of communication
**About Hays**
- 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.**My contact at Hays**
**Reference number**
681560/1
**Contact**
Phone: +41 44 225 50 00
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