How do I apply for the Internship: Scientist Global Regulatory Affairs position at GSK Stockmann and track my application?

We provide a direct link to the official application portal. You can apply directly here . Additionally, you can easily track this and other applications by clicking the bookmark icon to save it to your YGI Kanban board .

Is the internship at GSK Stockmann paid and what compensation can candidates expect?

Yes, this is a paid internship opportunity. Exact compensation details are typically finalized during the company interview process.

What are the working arrangements and expected duration for the Internship: Scientist Global Regulatory Affairs role?

This position is a full-time, structured as a not disclosed role, with an expected duration of 4.5 months.

What educational background or degree level is required for the Internship: Scientist Global Regulatory Affairs at GSK Stockmann?

Candidates are generally expected to be holding or pursuing the following degree levels: Master, PhD.

Does GSK Stockmann provide visa sponsorship or assistance for international applicants?

Regarding visa assistance and sponsorship for this role, the official status is currently listed as: Not disclosed.

Internship: Scientist Global Regulatory Affairs

GSK Stockmann

Found 2 weeks ago

Location

Wavre, Belgium

Duration (Months)

4.5 Months

Time

Full-time

Work Mode

Not disclosed

Salary

According to Belgian legal requirements, the internship will not be paid. However, some expenses will be reimbursed.

Visa Help

Not disclosed

Last Verified

2 weeks ago

Education

Master
PhD

Skills & Qualifications

Technical Skills

Regulatory Affairs
Engineering
Pharmacy
Biology
Chemistry
Bioengineering
technical regulatory documents
market specific requirements
Artificial Intelligence
Digital fluency

Soft Skills

interpersonal skills
communication skills
honesty
transparency

Job Description

A GSK internship offers you the opportunity to kickstart your career – to take on a real role with genuine impact! You’ll take on challenging, serious work on live projects or assignments. You’ll also get to learn from us, develop your skills and gain valuable experience for wherever the future takes you. What will you do? You will get tailored on-the-job training from Regulatory Affairs experts and take part in meaningful tasks that support vaccine development and lifecycle management, for example: Preparation and authoring of technical regulatory documents for vaccines in compliance with the applicable regulatory & scientific standards. Help compile market specific requirements. Support the preparation of responses to regulatory authority questions. Assist with deployment and adoption of new IT tools (Artificial Intelligence & Digital fluency) for GSK vaccines within Global Regulatory Affairs. Contribute to a variety of other regulatory and cross-functional projects

Requirements

regularly enrolled in a Master in Regulatory Affairs, Engineering, Pharmacy, Biology, Chemistry, Bioengineering or a related field in an Educational Establishment located in Europe
proficient in English
good interpersonal and communication skills
value honesty and transparency
mandatory & done in the framework of the curriculum, for which an agreement must be signed between GSK, the student and the Educational Establishment

Biology and Biotech

Biology Lab & Research

Languages

English

Nice to Haves

help bring safe, effective vaccines to patients around the world

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