20 melhores vagas de support engineer para porto (Contratando agora!)

Regulatory Affairs Specialist - Medical Devices
knok —Porto
- Período Integral
- Modelo Híbrido
Candidatura rápida
Join Our Loyalty Team
Pepco Tech Hub —Porto
- Período Integral
- Modelo Híbrido
Candidatura rápida
Há 7 dias
Business Data Analyst (Maintenance)
SBM Offshore —4100 Porto
- Mestrado
- Graduação
IFS-CMMS Implementation Lead (Temporary Contract)
SBM Offshore —4100 Porto
- Graduação
Senior Data Engineer
knok —Porto
- Modelo Híbrido
Candidatura rápida
Junior Oracle DBA
QUANTEAM —Porto
- Modelo Híbrido
Candidatura rápida
Intern - Enterprise Solutions & Continuous Improvement
SBM Offshore —4100 Porto
- Mestrado
Há 11 dias
Platform Engineer Tech Lead
Euronext —Porto
- Período Integral
- Mestrado
Java Lead Engineer – eDO Transport (Hybrid)
eDreams ODIGEO —Porto
- Modelo Híbrido
Senior Data Engineer
Keyrock —Porto
- Período Integral
Lead Engineer (Java) – eDO Transport (Hybrid)
eDreams ODIGEO —Porto
- Modelo Híbrido
Chief Electrician M/F - Seagoing
Mystic Cruises —Porto
Candidatura rápida
Forecast to Control and Accounting Department Manager
SBM Offshore —4100 Porto
- Mestrado
Há 13 dias
Rental Sales Agent
Europcar —Porto
- Período Integral
Senior HR Business Analyst
SBM Offshore —4100 Porto
- Graduação
HR Reporting and Analytics Manager
SBM Offshore —4100 Porto
- Graduação
Indirect Tax Analyst
SBM Offshore —4100 Porto
- Mestrado
- Graduação
Intern - Treasury Control Officer
SBM Offshore —4100 Porto
- Mestrado
Há 11 dias
Senior Data Engineer - Platforms
SBM Offshore —4100 Porto
- Mestrado
- Graduação
Sales Development Representative - German Market
TeamViewer Germany GmbH —4100 Porto
- Modelo Híbrido
- Mestrado
Candidatura rápida

Quero receber o alerta de ofertas mais recentes para support engineer em porto

Ao iniciar sessão na sua conta, concorda com os Termos de Serviço do SimplyHired e consente com a nossa Política de Privacidade e Cookies.

Explorar ofertas em mais locais

support engineer jobs near porto

Regulatory Affairs Specialist - Medical Devices

knok -
Porto

Candidatura rápida

Detalhes da oferta

Período Integral

Descrição completa da oferta

Learn About knok

At knok, we dare to lead and humanise the digital transformation of healthcare. We envision a world where everyone has timely access to quality healthcare through digital technology, creating a more equal society. We genuinely believe in it, and you can recognise it in every person who embraces this mission.

Through a Digital Front Door strategy, knok connects patients, providers and healthcare professionals in one place. Our API-first white-label platform enables a continuous, engaging and personalised healthcare experience for all conditions through a cutting-edge Patient Journey Engine.

With regular clinical practice as our main source of knowledge, we leverage ready-to-use data to improve care automation and increase financial savings. Since 2015, we have enabled more than 2.5 million clinical interactions in over 12 countries. Our platform is scalable and AI-ready, enhancing the power of data-driven care to deliver better outcomes during all stages of life.

Are you ready to join us in revolutionising healthcare and making a tangible impact on people's lives?

Responsibilities

Manage and support regulatory processes for medical devices (primarily within the EU - MDR);
Prepare technical documentation for certification (CE marking);
Ensure compliance with applicable regulatory requirements;
Collaborate with internal teams (product, engineering, clinical) to ensure regulatory alignment;
Support and maintain the Quality Management System (QMS), ensuring compliance with standards such as ISO 13485;
Liaise with notified bodies and other regulatory authorities;
Monitor regulatory changes and ensure internal implementation.

Requirements

3 to 5 years of experience in regulatory affairs for medical devices;
Proven experience in certification processes (e.g. CE marking under MDR);
Solid knowledge of quality management systems (e.g. ISO 13485);
Experience in preparing technical documentation (Technical File / Design Dossier);
Ability to work both independently and within a multidisciplinary team;
Fluency in Portuguese and English (mandatory).

Nice to Have

Experience with Software as a Medical Device (SaMD);
Knowledge of IEC 62304, IEC 62366 or ISO 14971;
Experience with regulatory audits and inspections;
Experience in digital health / health tech environment.

Candidatura rápida

Refine sua pesquisa

support engineer vagas para: porto

Regulatory Affairs Specialist - Medical Devices

Join Our Loyalty Team

Business Data Analyst (Maintenance)

IFS-CMMS Implementation Lead (Temporary Contract)

Senior Data Engineer

Junior Oracle DBA

Intern - Enterprise Solutions & Continuous Improvement

Platform Engineer Tech Lead

Java Lead Engineer – eDO Transport (Hybrid)

Senior Data Engineer

Lead Engineer (Java) – eDO Transport (Hybrid)

Chief Electrician M/F - Seagoing

Forecast to Control and Accounting Department Manager

Rental Sales Agent

Senior HR Business Analyst

HR Reporting and Analytics Manager

Indirect Tax Analyst

Intern - Treasury Control Officer

Senior Data Engineer - Platforms

Sales Development Representative - German Market

Quero receber o alerta de ofertas mais recentes para support engineer em porto

Related Searches

Explorar ofertas em mais locais

Ferramentas para Candidatos

Ferramentas da empresa

Procurar

Mantenha-se em Contacto