#Prismond Career
Location: Zurich / Zug
Country: Switzerland
Role: Subject Matter Expert (SME)
Team: Pharma / Biotech
Leading Quality Engineering activities for design, development and GxP manufacturing to ensure a high level of process and product quality
Develop, review and improve requirements, specifications, product plans and product drawings
Own and coordinate Qualification/Validation (incl. IQ, OQ, PQ) activities such as: Equipment qualification, production process validation, room qualifications etc.
Review/approve product and process change control documentation and specifications
Contribute to the development and improvement of design and manufacturing for existing and new products
Provide Technical Assessments to Change Controls/CAPA’s, Non-Conformities and Technical Suppliers Qualification
Master’s or Bachelor’s degree in Engineering, Bio-Pharma or another relevant life science discipline
In depth knowledge in Quality Engineering activities for design, development and manufacturing
Ability to communicate well verbally and in writing is essential
Demonstrated diplomacy and assertive skills in dealing with internal and external parties
A mature and disciplined approach to work is essential
Pronounced client focus and business orientation
Proficient use of MS Office suite and relevant database application
Prismond Group SA
Baarerstrasse 10
6302 Zug
Switzerland
Please note:
Please submit your online application in English or German language.
For further information, please contact our local Human Resources department.