3 bästa jobben som support coordinator i sweden (Rekryterar nu!)

Regulatory Affairs & Quality Lead (Region Europe)
Elekta —Stockholm
- Microsoft Office
- Budgetansvar
- Kommunikationsfärdigheter
- Betald semester
12 tim
Head of Learning
STIFTELSEN STOCKHOLM INTERNATIONAL SCHOOL —Stockholm
- Heltid
- Medicin
- Skrivkunskaper
- Engelska
10 tim
Environment and Energy Coordinator
SKF —Katrineholm
- Engelska
- Organisationsförmåga
- Kommunikationsfärdigheter
10 tim

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Regulatory Affairs & Quality Lead (Region Europe)

Elekta -
Stockholm

Ansök nu

Jobbinformation

12 timmar sedan

Förmåner

Betald semester
Privat sjukvårdsförsäkring

Kvalifikationer

Microsoft Office
Budgetansvar
Kommunikationsfärdigheter

Fullständig jobbeskrivning

Stockholm, Sweden

What You’ll Do At Elekta

As Regulatory Affairs & Quality Lead for Region Europe, you will play a critical leadership role in driving regulatory and quality excellence across the region. You will oversee regional regulatory submission strategies, ensure compliance with evolving legislation, and support the development and execution of quality systems aligned with global standards.

You will collaborate closely with regional teams, global stakeholders, and external authorities to enable safe and compliant delivery of Elekta’s products, while continuously improving processes and supporting organizational priorities.

Responsibilities

Lead and coordinate regulatory affairs and quality activities across Region Europe
Define priorities, set expectations, and align regional goals with global strategies
Drive execution of regional regulatory submission strategies and maintain the regulatory roadmap
Act as regional coordinator for regulatory submissions and provide guidance on legislation and interpretation
Represent Elekta in interactions with regulatory bodies and industry organizations
Support local regulatory and quality teams in submissions, compliance, and authority interactions
Establish, maintain, and improve regional processes, procedures, and quality systems
Ensure deployment of Elekta Quality Policy and adherence to applicable directives
Monitor and report on budget, planning, and logistics for the function
Approve documentation, including regulatory submissions and quality system changes
Ensure only compliant products are released for shipment
Participate in management reviews of regulatory and quality system performance
Mentor and develop team members, fostering a high-performing and collaborative environment
Drive continuous improvement initiatives and lead change within the organization
Deputize for the direct manager when required

What You’ll Bring

Proven experience in Regulatory Affairs within the medical device industry
Strong knowledge of European medical device regulations; familiarity with US FDA regulations is advantageous
Experience working with quality systems, supplier quality, or manufacturing engineering
Demonstrated ability to lead regulatory strategy and translate regulations into business requirements
Experience coordinating submissions and interacting with regulatory authorities
Strong leadership and team development capabilities
Ability to influence stakeholders and drive alignment across functions
Structured, problem-solving mindset with knowledge of quality tools and methodologies
Excellent communication skills, both written and verbal
High level of integrity and ability to build trusted relationships
Experience managing budgets and operational planning
Proficiency in Microsoft Office applications
Degree in engineering or a related field, or equivalent experience
ISO Auditor experience is preferred
Ability to work effectively in a multicultural, international environment

What You’ll Get

30 paid vacation days per year
4 additional Elekta days off
Defined contribution pension scheme
Private medical insurance
Lunch benefit
Contribution to wellness activities
Collaborative office environment with four days per week on-site alongside colleagues

Application process

We look forward to receiving your application. Please submit your CV in English We review applications on an ongoing basis, so we encourage you to apply as soon as possible. The last day to apply is 27 July 2026.

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Regulatory Affairs & Quality Lead (Region Europe)

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