Corporate Quality Assurance Documentation Associate - Saluggia, Italia - DiaSorin

DiaSorin
DiaSorin
Azienda verificata
Saluggia, Italia

2 settimane fa

Piero Bianchi

Inviato da:

Piero Bianchi

Reclutatore di talenti per beBee


Descrizione
DiaSorin Group Standard Job Description

Job
Corporate Quality Assurance Documentation Associate

Title

Job


Organizational Area:
Corporate

Kind of contract

Facts


Country / State:
Italy

  • Full Time /

Part Time:
Full time


Place of work:
Saluggia (VC)


  • Permanent / Temporary: Permanent

Home / Office based:
Hybrid work


Legal Entity:
DiaSorin S.p.
A


Job ID (1):


Professional Family:
Quality Assurance


Reporting To:
Senior Corporate Quality Assurance Documentation Specialist

Job


YOUR MISSION

Scope
Responsible for ensuring the proper management of Corporate quality system documentation

Main


YOUR CONTRIBUTIONS


Responsibilities:


  • Handle Corporate quality system documentation and the related Corporate Change Plans till documentation completion and implementation
- keep all the documentation updated and available

  • Prepare the documents with the support of the pertinent involved Company functions, as necessary and submit them for approval
  • Provide support as needed including procedure creation, tracking of documents or other activities
  • Ensure compliance with the Code of Ethics, the Quality Management System, the Company Policies and the Corporate Procedures.

YOU

Qualifications:


Education:
University degree or a professional qualification of an equivalent or higher standard, preferably scientific and technical.

Experience


Experience:


  • Minimum of 2 3 years' experience in the health care and sciences industry, preferably with diagnostic, medical devices or pharmaceutical prior knowledge/experiences.
  • Good knowledge of quality assurance within a regulated environment.

Technical Competencies:
Computer skills:, Google Apps, Excel, Word, PowerPoint, Outlook, Teams

Personal Strengths


Skills:


  • Personal characteristics : integrity, ethics, confidentiality, sincerity, diplomacy, openmind, sense of observation, perspicacious, persevering, resolute, selfconfident.
  • Abilities : analytical skills, ability to work equally as well on your own as in a team, aptitude to good interpersonal relationships, be organized, precise and flexible, optimal written and verbal communication skills. Pursue tasks with energy, drive, and initiative; even in a fastpaced environment

Languages:
Good spoken and written English.

Mobility


Travel availability:
na


Relocation availability:
na


Training required:


Internal training courses in relation to:

  • Good manufacturing Practice
- specific IVD MD processes (e.g. Reagents Manufacturing, Instrument development and Changes, Service and Marketing activities)


Specific Internal or external training course relation to:

  • Documentation management
  • Quality System Requirements (FDA CFR QSR 820, ISO 9001:2015, EN ISO 13485:2016/A11:202
  • Usability requirements,
(1) Assigned by Corporate Human Resources by Country.

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