Design Visual Inspection Qualification Program for the manual inspection program
Design, Qualification, Validation and Maintenance of equipment that supports Drug Product manufacturing and new Technology within Downstream Processing.
Work with other colleagues from around the network; coordinating activities, evaluating best practices in other areas, and working on continuous improvement project.
Support the development of Batch Documentation for DP Manufacturing.
Execute Batch Document / Run Equipment on the Process floor in coordination with other members of the team (Setup, Filling, Visual Inspection).
Provide support for Process Simulations (Microbial / Personnel) and Investigations.
Support coordination of daily work schedules and effectively organize needed support groups by attending the Tier meetings.
Investigate and Purchase New technologies to bring efficiencies to the organization and make the area a leader of innovation within the global network
Qualifications: University degree (MSc/BSc) in Biology, Pharmacy, Process engineering, or another relevant discipline
At least 3 years of work experience in the pharmaceutical or biotech industry (sterile manufacturing of pharmaceutical or biological components/finished products)
Demonstrated Microbiological knowledge and practical experience
Familiarity with Biotech Manufacturing processes and a good understanding of Downstream Unit Operations
Competent in analyzing complex situations and show practical problem solving capabilities
Effective verbal or spoken communication skills
Good communication skills in English; German language skills are highly desirable
Are you interested? Then apply now. For telephone inquiries, you can call Tanja Güntert, PhD at 044 225 41 07. Kelly Services (Schweiz) AG, Kelly Scientific Resources, Löwenstrasse 29, 8001 Zürich, Öffnungszeiten von Mo - Fr 8h00 – 12h00 / 13h30 – 18h00