To strengthen our team and meet the challenges posed by the market, we are looking for: **PHARMACEUTICAL TECHNICAL DIRECTOR** --------------------------------- Location: Estella (NAVARRA) Reference:DIR\-TEC\-FARMA\-NAVARRA Department: Regulatory Affairs **Our Offer:** * As a Pharmaceutical Technical Director (Qualified Person) at Messer Ibérica, you will play a key role in ensuring the safe, effective, and high-quality market availability of medicinal gases. * You will become part of an international, financially stable company committed to excellence in regulatory and quality compliance. * You will join a dynamic, inclusive, and collaborative work culture that promotes continuous improvement and professional development. * You will have access to specialized technical training and participate in strategic projects related to the authorization and operation of the Estella plant. * We offer a permanent contract, competitive compensation, and a benefits package commensurate with your experience and responsibilities. * On-site working model in Estella with some flexibility possible, within a technically rigorous and constantly evolving environment. **Your Mission:** Be responsible for the release and certification of batches of medicinal gases, ensuring strict compliance with current legislation and GMP guidelines, as well as acting as the main contact with competent authorities and leading regulatory activities related to production and quality control. **Your Responsibilities:** * Certify that each batch of medicines has been manufactured and controlled according to current regulations and marketing authorization. * Release batches prior to market placement. * Maintain traceability and documentation of batches for a minimum of 10 years. * Actively participate in validations, GxP audits, inspections by health authorities, and internal and customer audits. * Withdraw products from the market if necessary and collaborate in relevant investigations. * Sign off on control reports for imported products, where applicable. * Ensure regulatory compliance and contribute to the continuous improvement of quality and regulatory affairs processes. **Profile:** * University degree in Pharmacy (mandatory requirement). * Accredited training in Good Manufacturing Practices (GMP). * Minimum of 2\-3 years of experience in a similar role (as QP or within a regulated pharmaceutical environment). * Knowledge of regulations related to manufacturing, control, and release of medicinal products. * Strong organizational skills, results orientation, leadership, ethical commitment, and communication abilities. * Residence near Estella or willingness to relocate. * Proficient in English. Knowledge of German will be valued. If we have sparked your interest and you are ready for the challenge, please send us your application, indicating the reference (REF: DIR\-TEC\-FARMA\-NAVARRA) to: seleccion.es@messergroup.com