In sintesi
- Mansioni: Support e migliora il sistema di gestione della qualità in un ambiente dinamico.
- Azienda: Steelco S.p.A, leader nel settore della pulizia e disinfezione.
- Benefit: Ambiente di lavoro internazionale, benefit dedicati e opportunità di crescita.
- Altre informazioni: Unisciti a noi per un impatto reale nella salute e nell'industria farmaceutica.
- Perché questo lavoro: Fai la differenza nel settore sanitario con un team innovativo e aperto.
- Qualifiche: Esperienza in sistemi di gestione della qualità e ottima conoscenza dell'inglese.
La retribuzione prevista è compresa tra 60000 - 80000 € per anno.
- Employer
- Steelco S. p. A – HQ
- Location
- Via Balegante 27 Riese Pio X (TV) Italy
- Department
- Quality Assurance
- Type of work
Steelco and Belimed have joined forces to lead the way in advanced cleaning and sterile workflow solutions.
This partnership is powered by our united strengths: a dynamic product range, relentless innovation, utmost reliability, and an unmatched commitment to customer satisfaction.
As Steelco Belimed, we “Innovate with confidence”, as we set new industry standards to meet our customer’s needs offering high-quality products and comprehensive services for Infection Control and Life Science.
Your Role
The Quality Assurance Specialist will be part of the Quality Assurance team in Riese and will be responsible for implementing and maintaining the Company’s Quality Management System (QMS) in compliance with applicable industry standards.
- Tasks & Responsibilities
- Supports the organization in maintaining, improving and implementation of the Quality Management System.
- Supports the organization in controlling the cases in the CAPA Management System regarding
- Documentation quality
- Time deadlines
- Efficacy of Corrective and Preventive Actions
- Supports the operation of the CAPA Management System and understands the meaning of Non-Conformance handling processes such as audit findings, non-conformance, complaints, investigations and reportable incidents.
- Performs trainings of users in CAPA processes.
- Acts as interface between users of the CAPA Management Tool (super user), determines further developments of the CAPA Management Tool.
- Supports process owners in updating and improving the processes of the Quality Management System.
- Prepares and executes internal audits.
- Takes part during audits/inspections of Notified bodies or authorities.
- Supports the Business Units and plants in quality and regulatory questions.
Your Profile
- Directives, regulations and standards for medical devices quality systems: MDR 2017/745, EN ISO 13485, EN ISO 9001, EN ISO 14971, 21CFR Part 820 Quality System Regulation; Part 803 Medical Device Reporting; Part 806 Medical Device Corrections and Removals; Part 821 Medical Device Tracking etc.
- Excellent English language skills (Advanced C1).
- Strong team work skills.
- Hands on mentality.
- Flexibility, reliability, mediation skills, and a strong sense of responsibility.
Skills & Competencies
- Directives, regulations and standards for medical devices quality systems: MDR 2017/745, EN ISO 13485, EN ISO 9001, EN ISO 14971, 21CFR Part 820 Quality System Regulation; Part 803 Medical Device Reporting; Part 806 Medical Device Corrections and Removals; Part 821 Medical Device Tracking etc.
- Excellent English language skills (Advanced C1).
- Strong team work skills.
- Hands on mentality.
- Flexibility, reliability, mediation skills, and a strong sense of responsibility.
- Required Experience
- Previous experience in a similar role is prerequisite, particularly in quality management systems for medical devices and/or other regulated industries.
- 5 years of experience in an international acting company.
- Required Education
- Bachelor’s degree in or another similar scientific discipline.
- Our Offer
- Work in an international, fast-growing industry that makes a real impact on healthcare and pharmaceutical industry.
- Be part of an innovative and open-minded team.
- Join a company with a strong reputation and long-standing expertise in cleaning and disinfection solutions.
- We offer a people-focused work environment, with dedicated benefits and welfare initiatives.
Ready to make an impact? Apply now and join our team!
The personal data contained in your resume will be processed by Steelco S. p.
A., with registered office in Riese Pio X – TV, Via Balegante 27 (“Company”), for the selection process relating to this position or other similar positions.
Detailed information, including information on the rights recognized by the legislation on the protection of personal data, can be found in the information notice available on the Company's website on the “Careers” page (https://www. steelcogroup. com/it/careers/).
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Quality Assurance Specialist datore di lavoro: Belimed Group
Steelco S.p.A. è un datore di lavoro eccezionale, situato a Riese Pio X, dove i dipendenti possono contribuire a soluzioni innovative nel settore della salute e della scienza della vita. Offriamo un ambiente di lavoro collaborativo e orientato alle persone, con opportunità di crescita professionale e un forte impegno per il benessere dei nostri dipendenti. Unisciti a noi per fare la differenza in un'industria in rapida crescita che ha un impatto reale sulla salute globale.
