Diagnostics Product Development Specialist

Diasorin; Saluggia; In loco; EUR 33.000 - 40.000; Tempo pieno

Vantaggi offerti da questo lavoro

Free canteen

Well-being program

Supplementary pension

Supplementary healthcare coverage

Flexible benefits

Descrizione del lavoro

DiaSorin is seeking a Diagnostics Specialist in Italy to contribute to product development, risk assessment, and regulatory submissions. You will work with the R&D and regulatory teams to ensure compliance with internal SOPs and external standards, supporting prototype evaluation and supplier collaborations.

The role requires a scientific degree and at least two years in diagnostics or pharma, with fluency in Italian and English.

Competenze

• University degree in a scientific discipline.
• Two years experience in diagnostic or pharmaceutical companies.
• Knowledge of mandatory requirements for in vitro Diagnostic Medical Devices.
• Skilled with MS Office tools (Word, Excel).
• Basic statistical analysis with MiniTab or equivalent.
• DoE basic skills.
• Fluent in written and spoken Italian and English.

Mansioni

• Assist definition of master formulas of kit components and assay schemes for prototypes.
• Update team managers on progress from technical and timeline perspectives.
• Verify critical aspects and requirements of bench prototypes per GOP-SOP and quality standards.
• Contribute to defining product claims compliant with internal and external standards.
• Support project documentation and regulatory submissions.
• Collaborate on material definition and vendor interactions during development and industrialization.

Conoscenze

Fluent Italian and English

Office Tools

Basic statistics with MiniTab

DoE basic skills

Proactive mindset

Ability to work under tight timelines

Formazione

University degree in a scientific discipline

2 years experience in diagnostic/pharma

Strumenti

MiniTab

MS Office (Word, Excel)

Descrizione del lavoro

DiaSorin is seeking a Diagnostics Specialist in Italy to contribute to product development, risk assessment, and regulatory submissions. You will work with the R&D and regulatory teams to ensure compliance with internal SOPs and external standards, supporting prototype evaluation and supplier collaborations.

The role requires a scientific degree and at least two years in diagnostics or pharma, with fluency in Italian and English.