Regulatory Affairs Trainee

1 semana atrás


Vale de Cambra, Portugal Colep Consumer Products Tempo inteiro

We are looking for a Regulatory Affairs Trainee to join our R&D team to collaborate in the reception, verification, organization, management and update of raw and packaging materials as well other required documentation under the responsibility of R&D and other specific tasks.

**Main Activities and Responsibilities**:

- Support in the organization, maintenance and updating of the all documentation related to raw and packaging materials in the applicable software;
- Validate the defined fields of raw and packaging materials in the applicable software and fulfill the assigned ones;
- Ensures documentation compliance with company quality policies as well relevant regulations and standards;
- Cooperate with cross-functional teams, such as Product Development, Packaging Innovation, Regulatory Affairs, Product Industrialization and Marketing, Project Managers and others to gather information, address documentation needs, and support projects;
- Ensures the control of all Customer Black Lists and its introduction, maintenance and updating in the applicable software;
- Assist, when applicable, in creating and updating internal documents such as forms, guidelines, work instructions and others;
- Support the relevant teams in the communication with suppliers and customers when required;
- Support, when required, the requests from the teams regarding the preparation of Product Safety Data Sheets.
- Conduct periodic checks to keep the process under control and reconciling any possible discrepancies.
- Identify potential opportunities for streamlining documentation processes, improving data accuracy, and enhancing overall efficiency in documentation management.

**We are looking for**:

- Degree in Pharmacy, Chemistry, Chemical Engineering, Biochemistry, Biology or similar;
- Proficiency in Microsoft Office tools: Excel, PowerPoint, and Word;
- Fluency in English;
- Curious and proactive profile with good ability to learn;
- Good communication skills - verbal and written;
- Focused on goals, organised and meticulous;
- Good planning and organisational skills;
- Teamwork capabilities.

**What we offer**:

- Integration in an international and multicultural company with real opportunities for career development;
- Positive, informal and energetic work environment;
- Plenty of space for curiosity, creativity and growth;
- Health Service for employees and Employee Assistance Programme, with support in Psychological, Legal, Financial and Work-Life / Social areas.

**Job Type**: Internship
Contract length: 9 months

Pay: 1,000.00€ - 1,200.00€ per month



  • Parque Urbano de Miraflores, Portugal Zentiva Tempo inteiro

    We are looking for a Regulatory Affairs & Medical Affairs Specialist to join our team in Portugal. This is a dynamic role combining Regulatory Affairs, Medical Affairs, and Market Access responsibilities. You will play a key role in supporting product launches, ensuring regulatory compliance, and driving pricing and reimbursement processes. RESPONSIBILITIES...


  • Parque Urbano de Miraflores, Portugal Zentiva Tempo inteiro

    We are looking for a Regulatory Affairs & Medical Affairs Specialist to join our team in Portugal. This is a dynamic role combining Regulatory Affairs, Medical Affairs, and Market Access responsibilities. You will play a key role in supporting product launches, ensuring regulatory compliance, and driving pricing and reimbursement processes....


  • Parque Urbano de Miraflores, Portugal Zentiva Tempo inteiro

    We are looking for a Regulatory Affairs & Medical Affairs Specialist to join our team in Portugal. This is a dynamic role combining Regulatory Affairs, Medical Affairs, and Market Access responsibilities. You will play a key role in supporting product launches, ensuring regulatory compliance, and driving pricing and reimbursement processes. ...


  • Área Metropolitana de Lisboa, Portugal Hays Tempo inteiro

    Regulatory Affairs Specialist (m/f/d) | Empresa de Consultoria Farmacêutica A empresa onde vai trabalhar Integre uma empresa de consultoria para a Indústria Farmacêutica, assumindo a função de Regulatory Affairs Specialist. A sua nova função Este profissional será responsável pela preparação e submissão de pedidos de AIM (procedimento...


  • Paço De Arcos, Portugal Laboratório Edol - Produtos Farmacêuticos, S.A. Tempo inteiro

    O Laboratório Edol, empresa do Grupo Faes Farma, pretende reforçar a sua equipa de Assuntos Regulamentares com um Técnico de Assuntos Regulamentares – Mercado Nacional & Exportação (Regulatory Affairs Specialist) , para as suas instalações de Carnaxide. Esta vaga será para substituição de uma licença de maternidade. Principais...


  • Vila Nova de Famalicão, Portugal Continental Tempo inteiro

    Company Description Continental develops pioneering technologies and services for sustainable and connected mobility of people and their goods. Founded in 1871, the technology company offers safe, efficient, intelligent and affordable solutions for vehicles, machines, traffic and transportation. In 2024, Continental generated sales of €39.7 billion and...


  • Vila Nova de Famalicão, Portugal Continental Tempo inteiro

    Company Description Continental develops pioneering technologies and services for sustainable and connected mobility of people and their goods. Founded in 1871, the technology company offers safe, efficient, intelligent and affordable solutions for vehicles, machines, traffic and transportation. In 2024, Continental generated sales of €39.7 billion and...