7 Beste vacatures voor de functie van implementation division (nieuwe medewerkers gezocht)

RA Intelligence Officer
Terumo Europe —België
- Engels
- Onderzoek
- Communicatieve vaardigheden
1 dag
Mainframe System Engineer
Euroclear —België
- Weekendbeschikbaarheid
Mainframe DB2 System Engineer
Euroclear —België
- Secundair Onderwijs
Senior Kafka Engineer / Solution Designer
Euroclear —België
- Communicatieve vaardigheden
6 dagen
Enterprise Architect for Core Business Capabilities
Euroclear —België
- Engels
- Softwareontwikkeling
- ICT
System On Chip Embedded Software Engineer
NOKIA —België
- Voltijds
- Computerwetenschappen
- Master
- C++
Internship in GIZ’s EU Division
Deutsche Gesellschaft für Internationale Zusammenarbeit (GIZ) GmbH —Bruxelles Ixelles
- € 1.350 per maand
- Voltijds
- Microsoft Powerpoint
- Microsoft Excel
- Engels
5 uur

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RA Intelligence Officer

Terumo Europe
België

Nu solliciteren

Vacaturegegevens

1 dag geleden

Kwalificaties

Engels
Onderzoek
Communicatieve vaardigheden

Volledige vacaturetekst

At Terumo, we advance lifesaving medical technologies to benefit society. Are you eager to make a difference with us? Here, you’ll grow your expertise while staying true to your personal aspirations.

Guided by our Japanese heritage, we act with respect, take ownership, and pursue continuous improvement. If you see yourself in our values, keep reading; this might be the opportunity you're looking for

Department Info

EMEA Quality, Regulatory & Vigilance Division – Regulatory Affairs.

Job Summary

As a Regulatory Affairs Intelligence Officer, you support the Regulatory Affairs department in monitoring and analysing regulatory developments and ensuring compliance with applicable legislation and standards for medical devices.

In this role, you work closely with the RA Director and RA Intelligence Specialist to provide timely insights on regulatory changes and support the organisation in maintaining compliance across the EMEA region.

Job Responsibilities

Strategic Planning & Execution

Monitor developments and trends in European regulations for medical devices, including in vitro diagnostics
Follow regulatory and legal developments at national and international level (EMEA, US, Canada, Australia, China, etc.)
Support local offices on regulatory matters

Product Lifecycle Management

Monitor and analyse standardisation activities (ISO, EN, IEC and national standards)
Support implementation of updated standards and regulations within the organisation
Assist in impact analyses and implementation strategies for regulatory compliance

Stakeholder & Team Support

Communicate regulatory and standardisation updates to relevant departments
Support RA members in daily activities such as registration file preparation, technical file review and product labelling
Assist in training and onboarding of RA team members on legislation and standards

Performance & Process Improvement

Maintain and develop databases and systems related to regulatory information
Contribute to monthly and bi-annual reports on regulatory changes and trends
Support projects related to regulatory processes and compliance

Compliance & Quality

Support the organisation in ensuring compliance with applicable regulations and standards
Follow up on implementation of updated regulatory requirements
Liaise with national authorities under guidance of senior RA leadership

Profile Description

University degree in a scientific field, preferably medical or pharmaceutical oriented, or equivalent experience
Experience in a scientific environment (e.g. clinical research, biochemistry)
At least 1 year of experience in Regulatory Affairs within medical devices
Strong interest in analysing legislation and its impact on business

In addition, you recognize yourself in the following:

Accurate, well-organised and self-disciplined
Strong team player with excellent communication skills
Detail-oriented with strong analytical capability
Able to manage information, projects and regulatory data effectively
Good command of English; additional languages are an advantage

Offer

You will join an international Regulatory Affairs environment where you play an active role in monitoring regulatory developments, driving their implementation, and helping ensure compliance across the organisation.

Contact Person

Jarne Jans, Talent Acquisition Team

Working at Terumo means advancing healthcare with heart. Here, you are empowered to grow your own way, inspired to create to innovate, and supported as we get there together. Join us in shaping a healthier future for our patients, society, and each other.

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implementation division vacatures

RA Intelligence Officer

Mainframe System Engineer

Mainframe DB2 System Engineer

Senior Kafka Engineer / Solution Designer

Enterprise Architect for Core Business Capabilities

System On Chip Embedded Software Engineer

Internship in GIZ’s EU Division

More jobs to discover

Ik wil de nieuwste vacature-alerts ontvangen voor de functie van implementation division

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