CAREERS  |  METALTRONICA

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WORK WITH US

Open positions

1 SENIOR MAMMOGRAPHY APPLICATION SPECIALIST

Note: ONLY CANDIDATES WITH BELONGING TO PROTECTED CATEGORIES WILL BE CONSIDERED.
Mammography Application Specialist will deliver clinical and operational expertise by providing excellent education and training support to clinical end-users. In addition, as a clinical expert, he/she will facilitate evidence-based practice and support the commercial teams during sale visits highlighting the clinical value proposition.
Responsibilities and duties
• Provide on-site training and online support to customers showing best practices on installation protocols
• Support our distributors with product and clinical information
• Promote and Increase customer satisfaction
• Ability to drive solutions to customer satisfaction and collaborate across teams (sales, applications, service).
• Collection of feedback from the field and sharing with Product Management and R&D;
• Product presentation at customer sites and participation in exhibitions and workshops.
• Develop strong clinical relationships with KOLs within the Breast Imaging Segment.
Required Qualifications
• Bachelor's Degree as Radiographer or biomedical engineering degree with a minimum of two years experience in Breast Imaging Department workflow
• Must be willing to travel up to 80% on national and international territory
• High-level knowledge of written and oral English language
• High level of self-organization & planning
• Interpersonal skills and teamwork
Desired Characteristics
• Breast Imaging experience
• Mammography industry experience preferred.
• Good knowledge of a second language (Spanish, German or French is a plus). 
Place of work:
Pomezia (RM), industrial area (unreachable by public transport). This is not a smart working position. Pay grade and compensation will be assessed and commensurate with the candidate's actual work experience and qualifications.
In accordance with Laws 903/77 and 125/91, this search is destined for people of all ages, genders and nationalities, pursuant to Legislative Decrees 215/03 and 216/03.

1 ENGINEER TECHNICAL DOCS FOR DEVICE MASTER RECORD

Note: THE SPECIFIC REQUIREMENTS ARE MANDATORY: CANDIDATES WHO DO NOT MEET ALL THE REQUIREMENTS WILL NOT BE TAKEN INTO CONSIDERATION.
Responding to the Documentation and Technical Regulations Area Manager, the resource will be responsible for following everything related to the product-related documentation, in details:
  • Management of the Device Master Record (DMR), coordinating the archiving of the documentation for the realization of the product
  • Definition and update of assembly, testing, packaging, installation and related operating instructions
  • Elaboration and update of User Manuals for installers and technicians
  • Development and update of technical specifications and supplier documentation of mechanical, electrical and commercial components
  • Evaluation of alternative components following obsolescence
  • MINIMUM REQUIREMENTS:
  • - Degree in Biomedical / Electronic / Mechanical Engineering or Technical Expert with over ten years experience
  • - At least three-year experience in drafting technical product documentation
  • - Great confidence in the use of IT tools (especially office package, in particular word / excel but also solidworks, solid modeling programs and graphics programs like Photoshop)
  • - Good knowledge of English language
  • - Reliability, systematicity and good autonomy in organizing your work
  • - Predisposition to personal relationships and teamwork
  • - Any willingness to work overtime.
The resource will obviously be personally involved during company audits in supporting the Quality, Production and Warehouse departments.
Assignment and compensation will be assessed and in line with the candidate’s experience and skills.
In accordance with Laws 903/77 and 125/91, this search is destined for people of all ages, genders and nationalities, pursuant to Legislative Decrees 215/03 and 216/03.

ENGINEER TECHNICAL DOCS FOR DEVICE MASTER RECORD

Note: THE SPECIFIC REQUIREMENTS ARE MANDATORY: CANDIDATES WHO DO NOT MEET ALL THE REQUIREMENTS WILL NOT BE TAKEN INTO CONSIDERATION.
Responding to the Documentation and Technical Regulations Area Manager, the resource will be responsible for following everything related to the product-related documentation, in details:
  • Management of the Device Master Record (DMR), coordinating the archiving of the documentation for the realization of the product Definition and update of assembly, testing, packaging, installation and related operating instructions
  • Elaboration and update of User Manuals for installers and technicians
  • Development and update of technical specifications and supplier documentation of mechanical, electrical and commercial components
  • Evaluation of alternative components following obsol
  • MINIMUM REQUIREMENTS:
  • Degree in Biomedical / Electronic / Mechanical Engineering or Technical Expert with over ten years experience
  • At least three-year experience in drafting technical product documentation
  • Great confidence in the use of IT tools (especially office package, in particular word / excel but also solidworks, solid modeling programs and graphics programs like Photoshop)
  • Good knowledge of English language
  • Reliability, systematicity and good autonomy in organizing your work
  • Predisposition to personal relationships and teamwork
  • Any willingness to work overtime.
Assignment and compensation will be assessed and in line with the candidate’s experience and skills.
In accordance with Laws 903/77 and 125/91, this search is destined for people of all ages, genders and nationalities, pursuant to Legislative Decrees 215/03 and 216/03.

SEND US YOUR CV

Please, send us your CV and your personal information by filling out the registration form on your right; otherwise you can send us an e-mail indicating the open position of interest at:

hr@metaltronica.com

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