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Corporate Quality Assurance Documentation Associate

DiaSorin

Saluggia

In loco

EUR 35.000 - 50.000

Tempo pieno

30+ giorni fa

Descrizione del lavoro

DiaSorin is seeking a Corporate Quality Assurance Documentation Associate to manage quality system documentation and ensure compliance with regulations. The role requires a university degree and 2-3 years of relevant experience in healthcare or diagnostics, with strong analytical and communication skills. Join us to make a meaningful impact in global healthcare solutions.

Competenze

  • Minimum 2-3 years’ experience in healthcare and sciences industry.
  • Good knowledge of quality assurance in regulated environments.
  • Experience writing documentation for technical applications.

Mansioni

  • Ensure proper management of Corporate quality system documentation.
  • Handle Corporate Change Plans till their completion.
  • Ensure compliance with the Quality Management System and Company Procedures.

Conoscenze

Integrity
Analytical skills
Communication skills

Formazione

University degree (scientific or technical)

Strumenti

Quality System Requirements (FDA CFR QSR 820, ISO 9001:2015, ISO 13485:216)

Descrizione del lavoro

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Corporate Quality Assurance Documentation Associate

Published on: Jun 19, 2025

Job Category: Quality

Employment type: Regular Full Time

Diasorin is a global leader in diagnostic solutions, pushing the boundaries of science and technology to create cutting-edge tools that improve healthcare worldwide. With a legacy spanning over 50 years, we've earned our reputation for excellence by developing innovative diagnostic assays and instruments that are trusted by healthcare providers around the world.
Our broad offering of diagnostic tests and Licensed Technology solutions, made available thanks to ongoing investments in research, positions us as the player with the widest range of specialty solutions in the sector and identifies us as the "Diagnostics Specialist."
Why Join Diasorin?
Impactful Work: When you join Diasorin, you become part of a team that's dedicated to improving lives. Your contributions will directly impact patient care, making a meaningful difference in the world.
Global Reach & Innovation: Our work transcends borders. Joining Diasorin means collaborating with colleagues from all over the world, expanding your horizons, and contributing to global healthcare solutions at the forefront of the diagnostic industry.
Diverse and Inclusive Culture: We believe in the strength of diversity, and our inclusive culture reflects this commitment. We value your unique perspective and offer a supportive, collaborative environment where everyone can thrive.
Join Our Team: If you're passionate about innovation, diversity, and making a positive impact on healthcare, Diasorin is the place for you. We're looking for passionate and talented individuals who are ready to embrace new challenges and drive healthcare solutions forward.
Are you ready to be part of a dynamic team that's shaping the future of diagnostics? Join Diasorin and become a catalyst for change in the world of healthcare. Apply today and be a part of our exciting journey toward a healthier, more connected world. Together, we can make an impact!

Job Scope

Responsible for ensuring the proper management of Corporate quality system documentation

Key Duties and Responsibilities

- Handle Corporate quality system documentation and the related Corporate Change Plans till their 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.

Education, Experience, and Qualifications

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

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.

- recent experience writing documentation for technicalapplications

Quality System Requirements (FDA CFR QSR 820, ISO 9001:2015, ISO 13485:216)

Good manufacturing Practice

Documentation Management

Skills:

- Personal characteristics: integrity, ethics, confidentiality, sincerity, diplomacy, open-mind, sense of observation, perspicacious, persevering, resolute, self-confident.

- 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 fast-paced environment

Languages:

Good spoken and written English.

Diasorin is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status, and will not be discriminated against on the basis of disability.
In compliance with federal law, all persons hired will be required to verify identity and eligibility to work in the United States and Canada and to complete the required employment eligibility verification document form upon hire.
Diasorin is committed to providing reasonable accommodations for qualified individuals with disabilities. If you are a US or Canada candidate and require assistance or accommodation during the application process, please contact the North America Talent Acquisition Team at hrtalent@diasorin.com or 1-800-328-1482 to request an accommodation.
The above job description is intended to describe the general content, identify the essential functions, and set forth the requirements for the performance of this job. It is not to be construed as an exhaustive statement of duties, responsibilities, or requirements.
Diasorin reserves the right to modify or amend this job posting as needed to comply with local laws and regulations.
Please note that offers of employment at Diasorin may be contingent upon successful completion of a pre-employment background check and drug screen, subject to applicable laws and regulations.
This position is not eligible for partnership with a third-party search firm vendor without expressed, written consent from the Diasorin Human Resources Department.
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