Molecular R&d Validation Associate

Title

Job

**Organizational Area**: Molecular R&D
Kind of contract

Facts

**Country / State**: Italy
- Full Time / Part Time: Full time

**Place of work**: Gerenzano (VA) until November 2023. Bresso permanent location.
- Permanent / Temporary: Permanent

**Home / Office based**: Office

**Legal Entity**: DiaSorin Italia S.p.a

**Professional Family**: R&D

**Reporting To**: Molecular R&D Manager Europe

Job
YOUR MISSION

Scope
The Molecular R&D Validation Associate is responsible for conducting laboratory experimentations and investigations in compliance with Quality and Health&Safety procedures with the purpose of drafting a final report. He/she will follow all applicable regulations including, but not limited to, FDA, ISO, IVDD, and CMD/CAS requirements.

Main
YOUR CONTRIBUTIONS

**Responsibilities**:
Assisting in drafting protocols and executing laboratory research activities, in accordance with the company’s quality policies and procedures;
If necessary, suggesting new validation procedures while always respecting validation protocols objectives;
Once the protocol is approved, he/she will validate the test by conducting laboratory activities;
Analyzing the data based on performed tests and interpreting the results, interacting with internal and external scientists;
Supporting deviations management;
Defining a drafted report to be reviewed by scientists/managers;
Performing other laboratory activities when necessary;

**Qualifications**:
YOU

Experience

**Education**: Master’s degree in a scientific discipline

Personal Strengths

**Specialization**: Biology, biotechnology

Mobility

**Experience**: 1 year experience in a R&D molecular diagnostics laboratory.

**Technical Competencies**:
Basic knowledge of statistics (standard deviation and CV percentage);
Ability to work in compliance with the standard GMP procedures;
Basic knowledge on nucleic acid extraction;
PCR, RT-PCR and Real-Time PCR preferred;
Ability to exercise judgment within defined procedures to determine appropriate action;
Technical writing skills required;
Basic understanding of systems data management;
**Skills**:
Accuracy;
Analysis and problem solving capability;

Team work;

Time management;

Good communication skills;

Ability to work following rules and procedures

**Languages**: Basic knowledge of English language is required to read, draft and edit protocols, reports and working instructions.

**Travel availability**: N/A