Global Hardware Development Engineer Immuno - Saluggia, Italy - ITA 2023-008

Job Title

Global Hardware Development Engineer Immuno

Job Facts

Organizational Area
Corporate
Country / State
Italy
Place of work
Saluggia
Home/Office based
Office based

Professional Family: 

  • R&D - SD&I
Reporting To
Global Hardware Development Manager

Kind of contract

Full Time / Part Time
Full Time
Permanent / Temporary
Permanent
Job ID
ITA 2023-008

Job Scope

Your Mission

To provide a valuable operative and documentary contribution to the Team in accomplishing Hardware design and test activities, related to development of new instruments and improvement of existing instruments, through a professional, quality-driven and proactive attitude, with the target of building a solid Corporate know-how and in order to transfer to DiaSorin Customers the best quality in products and services

Main Responsibilities

Your Contributions

• Define, review and update hardware requirements (high-level and low-level) deriving from higher level requirements, from market feed-back or from regulatory/safety requirements
• Review the associated hardware specifications
• Interact with the other development areas within the Team (“Software”, “Consumables” and “Assay Integration”), as per the joint development/improvement tasks
• Manage hardware installations aimed at hardware testing activities
• Edit, review and perform hardware verification/validation plans
• Contribute actively to troubleshooting and defects fixing with the instrument Development Partners
• Investigate on anomalous and/or uncommon situations
• Interact with other Company functions, in order to provide team’s know-how and support to problem solving
• Ensure compliance with the Code of Ethics, the Quality Management System, the Company Policies and the Corporate Procedures

Qualifications Experience Personal Strengths Mobility

You
Education
Master’s Degree
Specialization
Engineering or equivalent
Experience

• 2-5 years’ experience in a technical field is a plus
• Previous experience in IVD (In Vitro Diagnostics) and/or highly regulated FDA environments and biotechnology industry experience is highly appreciated

Technical Competencies

• Knowledge of GMP (Good Manufacturing Practice) is appreciated
• Seasoned experience using Microsoft Office package

Skills

• Accuracy, comprehension of technical issues
• High problem-solving and decision-making capability
• Effective analytical skills
• Interdisciplinary thought and quality awareness
• Well organized, ability to work well independently as well as part of a team
• High commitment and willingness to learn
• Positive, proactive and open-minded attitude
• Focus on results

Languages
Fluent spoken and written Italian and English
Travel Availability
Travels may be required (max.: a few days every 1-3 months)
Relocation Availability
N/A
Training Required

Induction Program Once Hired

Benefits

We Offer You

As for Company Policy