EMEA Quality Customer Service Program Manager
Varian Medical Systems Visualizza tutti gli annunci
- Italia
- Tempo indeterminato
- Full time
- Elaborates, analyzes and implements quality concepts, methods, tools and procedures as part of an effective agile/lean-oriented Quality Management System, in a specific quality area, or in an assigned organizational unit.
- Creates transparent and open environment for quality culture together with management.
- Gives guidance that risks are identified, considered and controlled throughout the design and the use of the Quality Management system.
- Creates real-time transparency for ad-hoc analysis, instant decision making, preventive action and continuous improvement.
- Drives innovative digital solutions to improve quality by thinking outside of the box, coaching and fostering the application of creativity methods.
- Trains employees in a specific quality area.
- Coaches team members of agile/lean projects or even leads projects e.g. as a CAPA expert, owner, reviewer
- Ensures, implements and assesses quality-related standards and regulatory requirements in a specific quality area, or in organizational unit(s) assigned.
- Analyzes and improves a series of process steps by applying appropriate methods like Value Stream Mapping, Root cause analysis etc..
- Coordinates a group of quality-related staff without leading the team.
- Ensures effective cooperation with both internal and external stakeholders.
- Coordinates an assigned international/national quality network in a specific quality area.
- Academic Background: Bachelor’s or master’s degree in engineering, Biology, or other STEM disciplines (Science, Technology, Engineering, and Mathematics).
- Professional Experience: Minimum of 5 years of experience within the Medical Device industry, specifically in Quality Management roles (e.g., Quality Manager, Quality Responsible or Quality Specialist, Consultant or Auditor).
- Quality Assurance: Strong working knowledge of ISO 13485 standards, Proven track record in managing Corrective and Preventive Actions (CAPA) processes, experience in planning, conducting, documenting internal audits and related follow-up, experience in hosting external audits (i.e. notified bodies, competent authorities) and related follow-up
- Regulatory Expertise: working knowledge of Medical Device Regulation (EU) 2017/745
- Mindset: A curious and proactive individual with a strong desire to learn and innovate. Attitude towards teamwork in an international and multicultural environment
- Mobility: Available for travel approximately 20% of the time (visiting Siemens Healthineers/Varian sites and conducting occasional on-site client audits).
- Location: Based in Milan, Italy.
- Language Skills: Proficiency in English (Fluent/Professional level) is highly desirable. French is a plus