QARA Manager (big pharma OTC)

- Support the development of the CMCD strategy for certain products of the business unit, both mature and new launch, to ensure globally approvable dossiers. - Responsibility is shared across global and local markets. - Work closely with Regulatory to develop effective Regulatory and CMC strategies. - Collaborate with R&D, Product Supply, and Regulatory to ensure the timely compilation of high-quality CTD Module 3 and QOS documents. - Support responses to Quality questions from Regulatory Health Authorities. - Support the core Technical Sub Teams from feasibility, through all clinical stages, license application, and post-approval LCM. - Effectively manage post-approval change and product lifecycle. - Drive continuous improvement. - Maintain and implement knowledge of current industry requirements and best practices for CTD Module 3 and QoS or equivalent. - Coach and mentor junior staff members cross-functionally. Requisitos del puesto: Academic background in life sciences. Very high proficiency in spoken and written English, as this is a global position. Significant experience in CMC/Module 3 creation and response to questions. Experience in QA and RA departments for global markets, including but not limited to North America, South America, Europe, Australia, ASEAN, and the Middle East. Experience leading projects in the QA department. Experience managing teams. Formación: Licenciado : Ciencias Químicas Idiomas: Inglés : C1 Conocimientos: gmp , glp , gdp , gcp Experiencia: 4 años Tus beneficios: Attractive compensation package with extensive social benefits. Hybrid position with great flexibility. You will belong to a leading big pharma company in its sector.