Assay Transfer & Validation Technician

Diasorin

Saluggia

In loco

EUR 30.000 - 37.000

Tempo pieno

7 giorni fa
Candidati tra i primi
Generatore di candidature

Non inviare un curriculum generico — genera un curriculum e una lettera di presentazione personalizzati per questo specifico ruolo.

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Vantaggi offerti da questo lavoro

Permanent contract
CCNL classification
Supplementary pension fund
Supplementary healthcare coverage
Company welfare plan
Free canteen
Well-being program

Descrizione del lavoro

Diasorin is a global leader in immunodiagnostic and molecular diagnostic solutions seeking a Diagnostics Specialist for Manufacturing and QC Immuno Liaison activities. You will perform validation batches, immunometric QC testing, and support industrialization processes under GMP and Quality Procedures.

The role involves collaboration across sites for technology transfer, validation activities, and continuous improvement.

Competenze

  • Higher diploma or university degree in technical-scientific field.
  • Experience in biomedical labs or medical devices is preferred.
  • Good written and verbal communication skills.
  • Good interpersonal and organizational skills.
  • Strong English knowledge.

Mansioni

  • Ensure compliance with Code of Ethics, QMS and company policies.
  • Prepare validation batches and pilots per GMP and Quality Procedures.
  • Perform immunometric QC testing and data evaluation.
  • Support drafting of industrialization documents.
  • Collaborate on technology transfer activities and validation efforts.
  • Support in data collection and validation planning and change management.

Conoscenze

Communications skills
Good English
Interpersonal skills
Organizational skills

Formazione

Higher diploma or university degree in technical-scientific field

Strumenti

Microsoft Office

Descrizione del lavoro

Diasorin is a global leader in immunodiagnostic and molecular diagnostic solutions seeking a Diagnostics Specialist for Manufacturing and QC Immuno Liaison activities. You will perform validation batches, immunometric QC testing, and support industrialization processes under GMP and Quality Procedures.

The role involves collaboration across sites for technology transfer, validation activities, and continuous improvement.

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