Senior Specialist Quality & Regulatory Affairs EMEA

Location: Càrcer

Supports EMEA-wide QA/RA operations, participating to EMEA QA/RA Management meetings, documenting EMEA policies, accompanying the Snr. Director QA/RA EMEA to perform quality visits to countries and issue gap analysis, ensures CAPA follow-up on identified issues and support countries in implementing solutions within the Global Distribution Group Henry Schein Sites in EMEA.

ESSENTIAL DUTIES AND RESPONSIBILITIES:

Supports EMEA-wide QA/RA operations, documenting EMEA policies and provides support to implement the EMEA Quality Management System.

Supports to perform quality & regulatory visits and /or audits to countries and issues gap analysis, ensures CAPA follow-up and related documentation on identified issues and support countries in implementing solutions.

Organizing virtual, onsite, and offsite regional meetings, including logistics, agendas and close follow-up on decided actions with related functional / country QA/RA Lead.

Support and assistance to Exec. Director QA & RA EMEA and the EMEA QA/RA Team

Support to multiple projects, tracking timelines, and ensuring successful outcomes for EMEA-wide QA/RA initiatives.

Maintenance of eQMS and Quality Document Management Tool

Oversight of change control activities and CAPA follow-up, timely closure

Provides support to the country QA/RA Teams in Quality related topics to ensure compliance with GDP and MDR.
Implementation of regulatory requirements and continuous improvement, support to ongoing transformation projects and product launch activities

Support roll-out eQMS implementation in identified countries. o Inspection readiness initiatives and to roll- of required tools o Conduct and oversee quality training and compliance communications.

Assists PRRC and EC Rep responsibilities such as adverse event reporting, post-market surveillance and FSN management

Other tasks and projects as needed

Physical

Activities:

Job holder based in any country in EMEA

Home based – ready to travel regularly (up to 30%)

QUALIFICATIONS:

Experience:

Quality Management, Project Management experiences, Medical Device

Experiences, Pharmaceutical (GDP) experience is a plus

MDR /IVDR Regulations/ ISO 13485

Validation of (computerized systems) and Risk management (FMEA) knowledge is a plus

Education:

Bachelor’s degree in Life Sciences, Pharmacist, Biomedical Engineering, Business management or a related field.

Specialised Knowledge and

Skills:

Knowledge and understanding of Quality Management Systems and Project Management

Quality System process implementation and maintenance to meet ISO 13485:2016; GDP and MDR.

Solution oriented, problem-solving attitude, pragmatic, high adaptability and flexibility

Ability to work in a matrix, regional environment with different departments and countries

English speaker

Good communication skills and stakeholder management

Other:

Balances a sense of urgency of time pressures with adherence to all regulatory requirements.

Sensitive in dealing with confidential Information

Demonstrates advanced oral and written communication skills

Must be fluent in written and spoken English

Information on pay transparency pursuant to Directive (EU) 2023/970

Please note that we comply with the relevant legal obligations regarding pay transparency, in particular those set forth in the EU Pay Transparency Directive (Directive (EU) 2023/970) and its respective national implementation.

In this context, we will inform you of the starting salary or the corresponding salary range for the advertised position no later than before the first job interview or before a personal discussion of your application. This information is based on objective, gender-neutral criteria established for the position in question.

Please note that we will not ask about your current or previous salary during the rest…