Software QA Engineer - Thermo Fisher Scientific

Farkas Kiss Endre legjobb állása Thermo Fisher Scientific

Bewerbung fur Software QA Engineer - Thermo Fisher Scientific

Levél szövege

Lieber Thermo Fisher Scientific!

Ich möchte mich bei Ihrem Unternehmen als Software QA Engineer - Thermo Fisher Scientific bewerben. 
Ich bin ein Fullstack-Entwickler, bei dem ich meine 10-jährige Erfahrung mit verschiedenen Technologien einsetzen kann.

Ich habe meinen Lebenslauf an diese E-Mail angehängt.

Wir freuen uns darauf, von Ihnen zu hören!


Endre Farkas Kiss "Sodika"
Java and PHP Fullstack Developer, Nudist, Vlogger

https://www.linkedin.com/in/farkas-kiss-63bb9210a
https://sodika.org

Álláshirdetés szövege

Deine Rolle im Team
Provide daily support to the development and commercial operations, including software validation packages, product monitoring, risk assessment and CAPA and problem investigations.
Ensure Software development design control, verification/validation is in compliance with applicable QMS and regulations (e.g ISO 27001, USFDA regulations (e.g. 21CFR Part 11), Eudralex Volume 4 Annex 11, ISO27001, SOC2, EU GDPR, among others)
Represent Quality Assurance in sprint planning, reviews, retrospectives, release planning, demos and other Scrum-related activities
Develop and implement appropriate product quality/process improvement strategies with guidance from multi-functional team based on risks and opportunities - e.g. continuously improve Software Development Life Cycle processes with the multi-functional team
Work closely with Software development team, Software testing team and product owners to increase the reliability of the software via improving test automation infrastructure/test coverage and standard processes to guarantee a quality user experience to our customers.
Responsible for the qualification of software vendors and service providers - verification/validation
Support the Quality Management System - e.g. quality plans/initiatives, change control/management, CAPAs, Supplier management, training, and audit program
Participate as a Quality resource/facilitator for audit programs including internal routine audits and external audits (e.g. ISO, Customer, etc.). Responsible to support the maintenance of the necessary multi-site certification by participating in Audits (for e.g. but not limited to ISO 9001, ISO 27001)
Acts as the Quality representative of the Product related CAPA review board (CRB), supports the organization to perform Root cause analysis and corrective/preventive action review
Engage in quality initiatives to continuously elevate the quality culture and drive process improvements, support quality metrics and reporting for management reviews

Technologien und Skills
Review Board
.NET
Java
Azure DevOps
Power BI

Unsere Erwartungen an dich:
Qualifikationen
Knowledge in regulations such as ISO9001, ISO27001 and 21CFR part 11
Excellent understanding of software lifecycle
Strong written and oral communication skills in English
Knowledge of the following .NET and JAVA would be a plus
Enjoys working independently and as part of a team, adaptability, diligent and positive approach

Erfahrung
Experience working with Azure DevOps dashboards & Power BI is welcomed

Ausbildung
Proven experience working in regulated laboratory environment - suitable for candidate's with various education background (biology, chemistry, biomedicine etc.)

Benefits
Bonuszahlungen