Corporate Quality Assurance Documentation Associate - Saluggia, Italia - DiaSorin
Descrizione
DiaSorin Group Standard Job DescriptionJob
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
- 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 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,
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