Descripción de la oferta
Do you want to be part of a team with a real impact on global health?Por favor, lea detenidamente la información de esta oferta de empleo para entender exactamente qué se espera de los posibles candidatos. At Noucor , a chemical and pharmaceutical company, we offer you the opportunity to lead projects that reach more than 100 countries worldwide . We are currently looking for a Clinical R&D Quality Assurance Technician to join Noucor’s Quality team. Main Tasks: Ensure that all processes related to clinical trials are performed in compliance with GCP (Good Clinical Practice) and applicable quality standards. Provide QA support to clinical trial activities, including documentation review and quality oversight of internal teams and external partners (CROs, service providers). Evaluate and manage quality issues, deviations, CAPAs, change controls and complaints related to Clinical Trials. Support quality activities related to Investigational Medicinal Products (IMPs) in collaboration with Pharmaceutical Development and Analytical Development. Maintain awareness of applicable quality regulations and compliance requirements impacting clinical development and R&D activities. Requirements: Degree in Pharmacy, Chemistry, Biology, or similar. Fluent in English and Spanish. Experience in Good Clinical Practices (GCP); knowledge of GMP requirements for IMPs in clinical trials (formerly Annex 13). Good command of MS Office. High willingness to learn and take on new challenges and responsibilities. Motivation, teamwork, and good communication skills. We Offer: Work within a great team of professionals with a very good work environment. Innovative work environment focused on continuous improvement. Continuous learning and development. Competitive benefits package and flexible schedule. Offices in Palau-solità i Plegamans. Competitive salary. Interested in joining us? At Noucor , we believe in the value of diverse teams. xcskxlj We therefore welcome and consider all applications regardless of gender, age, background, sexual orientation, gender identity, or any other personal characteristic. If you meet most of the requirements and are motivated by the project, we would be pleased to hear from you.
