Regulatory Affairs Trainee

GSK; Lisboa; Híbrido; EUR 8900 - 11 000; Tempo integral

Vantagens oferecidas por esta oferta de emprego

Structured training

On-site with hybrid options

Resumo da oferta

GSK in Portugal is offering an 8-month Regulatory Affairs trainee programme. You will join the Regulatory Affairs team as a dedicated resource for a key internal project, taking ownership of regulatory activities required to support its successful implementation.

We value curious learners, strong communicators and people who pay attention to detail. You will gain hands-on experience, guided learning and exposure to EU/national procedures, with emphasis on attention to detail, communication, and

Qualificações

• Degree (Bachelor or Master) in Pharmacy, Pharmaceutical Sciences, Life Sciences or related subject.
• Fluent Portuguese and strong English written and spoken skills.
• Good organizational skills and ability to manage priorities and deadlines.
• Strong attention to detail.

Responsabilidades

• Prepare and submit regulatory variations and dossier updates through national and European procedures.
• Track and follow up regulatory procedures with the national competent authority (INFARMED, I.P).
• Maintain and update internal regulatory databases and trackers.
• Support updates to product information documents (SmPC, PILs, labeling).
• Review and approve packaging artwork from a regulatory perspective.
• Collaborate cross-functionally to deliver Regulatory Affairs activities and priorities.

Conhecimentos

Agile Planning

Business Acumen

Change Management

Digital Fluency

Learning Agility

Problem Solving

Regulatory Strategies

Formação académica

Bachelor or Master in Pharmacy or Life Sciences

Descrição da oferta de emprego

Position Summary

You will join our Regulatory Affairs team in Portugal as a trainee for a 8-month programme. You will act as the dedicated resource for a key internal project, taking ownership of the regulatory activities required to support its successful implementation. We value curious learners, strong communicators and people who pay attention to detail. This role offers guided learning, real responsibility and the chance to make a meaningful impact while growing your regulatory skills at GSK. You will help us unite science, technology and talent to get ahead of disease together.

Responsibilities

This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following:

• Prepare and submit regulatory variations and dossier updates through national and European procedures.
• Track and follow up regulatory procedures with the national competent authority (INFARMED, I.P).
• Maintain and update internal regulatory databases and trackers.
• Support updates to product information documents, such as summaries of product characteristics, patient information and labelling.
• Review and approve packaging artwork from a regulatory perspective.
• Collaborate cross-functionally to deliver strategic Regulatory Affairs activities and business priorities.

Why You?

Basic Qualification

• Degree (Bachelor or Master) in Pharmacy, Pharmaceutical Sciences, Life Sciences or related subject.
• Fluent Portuguese and strong English written and spoken skills.
• Good organizational skills and ability to manage priorities and deadlines.
• Strong attention to detail.
• Good communication skills and ability to work in a team.
• Dynamic and proactive
• Interest in a career in regulatory affairs and readiness to learn.

Preferred Qualification

• Postgraduate training or coursework in Regulatory Affairs.
• Previous internship or work experience in regulatory affairs or pharmaceutical industry.
• Familiarity with national and European regulatory procedures (e.g. national, Mutual recognition Procedure, Decentralized Procedure and Centralized Procedures).
• Experience with regulatory databases or document management systems.
• Basic understanding of packaging and labelling requirements.
• Ability to work independently with initiative and adaptability.

Work Arrangement

This role is on-site in Portugal with hybrid working options depending on business needs and line manager agreement.

What we offer

You will receive structured training and coaching. You will work alongside experienced regulatory professionals. You will gain hands‑on experience across regulatory processes and exposure to cross‑functional projects. This role supports career growth and practical development in an established global company.

Skills

Agile Planning, Business Acumen, Change Management, Digital Fluency, Learning Agility, Problem Solving, Regulatory Strategies

This is a temporary internship opportunity focused on professional development. Any reimbursement, scholarship, allowance, or financial support will be provided in accordance with applicable local laws, regulations, and GSK site policies. More detailed information will be provided during the recruitment process.Esta é uma oportunidade temporária de estágio, com foco no desenvolvimento profissional. Qualquer reembolso, bolsa, subsídio ou outro tipo de apoio financeiro será atribuído de acordo com a legislação local aplicável, bem como com os regulamentos e políticas da GSK no respetivo local. Informações adicionais serão fornecidas durante o processo de recrutamento.

Why GSK?

Uniting science, technology and talent to get ahead of disease together.GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases - to impact health at scale.People and patients around the world count on the medicines and vaccines we make, so we're committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.