Qualified Person and Quality Assurance Specialist - Santarém

Santarém Indefinido Trabalho Remoto / Híbrido Consultar descrição da função
Pharmaceutical organization operating under EU‑GMP standards, focused on high‑quality production and global distribution.Strategic Qualified Person & Quality Assurance role with high responsibility and strong development prospects.

Added 23/03/2026

  • Pharmaceutical organization operating under EU GMP standards
  • Hybrid QP/QA role with impact, responsibility, and growth potential

Sobre o nosso cliente

Our client, a fast‑growing organization operating in the highly regulated pharmaceutical and healthcare sector, is strengthening its Quality function and is currently recruiting a GMP Quality Assurance professional to reinforce its in‑house Qualified Person (QP) capabilities.

Descrição

  • Support and contribute to Quality Assurance activities within an EU‑GMP environment, ensuring full compliance with pharmaceutical quality systems and regulatory requirements;
  • Strengthen QP‑related processes, assuming responsibilities aligned with the Qualified Person scope (for candidates who already hold, or will soon obtain, QP certification);
  • Ensure robust implementation, maintenance, and continuous improvement of GMP standards across production, packaging, logistics, and distribution operations;
  • Work collaboratively with cross‑functional teams, promoting a culture of quality, operational excellence, and regulatory compliance;
  • Act proactively in identifying risks, proposing corrective and preventive actions, and supporting decision‑making with strong analytical rigor;
  • Serve as a business partner to internal stakeholders, ensuring alignment between quality requirements and operational needs, and supporting the organization's global expansion.

Perfil ideal

  • University degree in Pharmaceutical Sciences or related field, with QP Certification from the Ordem dos Farmacêuticos (or in the process of being obtained);
  • Experience in Quality Assurance roles within the pharmaceutical industry;
  • Solid knowledge of pharmaceutical quality systems, GMP regulations, and applicable regulatory frameworks;
  • Strong communication and influence capabilities, with the ability to partner with multidisciplinary teams;
  • Excellent analytical mindset, ethical standards, and strong sense of confidentiality;
  • Ability to work collaboratively in a dynamic and evolving environment;
  • Proficiency in spoken and written English;
  • Location: Santarém.

Vantagens

Excellent opportunity to join a rapidly expanding organization in the pharmaceutical and medical cannabis sector, operating with EU‑GMP standards and global reach. You will integrate a skilled, collaborative, and highly motivated team, contributing to projects with real impact on patient care worldwide, and benefiting from a dynamic environment with room for growth, ownership, and innovation.

Pesquise mais Ofertas
Joana Gouveia Lopes
Quote job ref
JN-032026-6977746

Resumo da Função

Setor
Healthcare & Life Sciences
Subsetor
Qualidade
Adicionar indústria
Healthcare / Pharmaceutical
Localização
Santarém
Tipo de contrato
Indefinido
Nome do Consultor
Joana Gouveia Lopes
Referência da Oferta
JN-032026-6977746
Tipo de trabalho
Trabalho Remoto / Híbrido

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