20 annunci per il ruolo di quality specialist - veneto (recruiting in corso)

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Quality Assurance Specialist

Belimed -
Riese Pio X, Veneto

Candidati adesso

Dettagli della posizione

Tempo pieno
1 giorno fa

Qualifiche

Inglese
Laurea triennale
Pulizie

Descrizione completa della posizione

Quality Assurance Specialist

Employer
Steelco S.p.A – HQ

Location
Via Balegante 27
Riese Pio X (TV)
Italy

Department
Quality Assurance

Type of work
Full time (8.00 - 17.00)

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 SteelcoBelimed, 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 controling 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

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!

Apply online

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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