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Guarantees cGMP compliance in all activities and systems related to Projects and Products execution. Assures that working practices are streamlined and aligned with the actual needs of each project. Implements policies, procedures and methods to evaluate and to continuously improve the quality of products and operations throughout the products lifecycle. Provides global supplier qualification services in support of new product introduction and existing products. Collaborates with suppliers and Procurement to assure the quality of their products, materials, components and/or operations.  

- Develop detailed civil engineering designs and plans for pharmaceutical facilities; - Conduct site assessments and feasibility studies for new construction projects; - Collaborate with architects, mechanical engineers, and other stakeholders to ensure integrated project delivery; -

- Perform qualitative and quantitative analyses of compounds, including drug substances, drug product intermediates and drug product. - Recommend the analytical characterization package (Chemical, physical, performance) and control the quality and accuracy of the data in compliance with legislation and regulatory standards of Quality, HSE and cGMP policies. - Promote the scientific excellence and innovation in the Analytical area and contributes with technical expertise to expand the Intellectual Property,...

The Director of Compliance & Innovation will be responsible for the global compliance Strategy and oversight across Hovione´s network, ensuring the highest GMP standards and regulatory readiness either for the current or new business areas. This is a new role that will strengthen our global compliance profile, drive inspection readiness, and support the integration of new business modalities – particularly in biotechnology and aseptic manufacturing.