Position Overview: We are looking for a motivated and detail-oriented Quality Associate to join a pharmaceutical company. In this role, you will play a critical part in ensuring compliance with GxP standards for medicinal products, supporting operations across Europe and worldwide. Key Responsibilities: Qualification and Oversight: Evaluate and qualify healthcare professionals, pharmacies, and clinical trial sites to receive medicinal products in multiple regions globally. Ensure all sites meet GxP requirements and maintain up-to-date documentation. Complaint Management: Investigate customer complaints, perform root cause analysis, and implement corrective and preventive actions where necessary. Ensure timely and accurate reporting of findings. Deviation Management: Monitor deviations, ensure thorough investigations, and track the implementation of corrective actions to prevent recurrence. Quality Support: Assist the global Quality Team in maintaining compliance with internal procedures and regulatory requirements. Provide input on process improvements and support audits as needed. Documentation and Reporting: Maintain accurate records for all quality-related activities, ensuring compliance with GxP standards and internal policies. Prepare reports, summaries, and other documentation as required by internal teams and regulatory authorities. Requirements: University degree in Natural Sciences (e.g., Biology, Biochemistry, Pharmacy) or Quality Management. Minimum of 2 years’ experience in a GxP-regulated environment, preferably within the pharmaceutical, clinical trial, or life sciences sector. Strong command of English, both written and spoken, with the ability to communicate effectively in an international and multicultural environment. Strong attention to detail and commitment to maintaining high-quality standards. Why This Role Matters: As a Quality Associate, you will contribute directly to ensuring that medicinal products are delivered safely and compliantly to healthcare professionals and patients worldwide. Your work will support global operations and uphold the highest standards of quality and regulatory compliance, making a meaningful impact on patient care and clinical research.