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Qualified person and quality assurance specialist - santarém

Santarém
Michael Page
Anunciada dia 28 março
Descrição

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. 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. DescriptionSupport 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. ProfileUniversity 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; Job OfferExcellent 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.#J-18808-Ljbffr

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