Molecular R&d Validation Associate - Gerenzano, Italia - DiaSorin

DiaSorin

Azienda verificata

Gerenzano, Italia

2 settimane fa

Inviato da:

Piero Bianchi

Reclutatore di talenti per beBee

Descrizione

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