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- Support the execution of Learning & Development processes (e.g., learning needs analysis, training design, and effectiveness measurement). - Participate in L&D projects and initiatives with significant impact on business. - Assist in creating training materials, modules, and e-learning content. - Collaborate with subject matter experts to develop engaging learning...

As a CQV (Commissioning, Qualification, and Validation) Senior Engineer at Hovione, you lead complex engineering initiatives across pharmaceutical and chemical manufacturing environments. The role bridges technical excellence, regulatory compliance, and cross-functional collaboration to ensure robust, GMP-compliant systems and equipment. Role Overview You are specialized in the design, implementation, and qualification of manufacturing systems, utility infrastructures, and automation technologies. Your work ensures that...

This role is responsible for managing the full contract lifecycle. It combines scientific knowledge with commercial insight to identify new opportunities, support client engagement, and drive business growth — all while ensuring compliance with internal and external standards.    Key Responsibilities: 

Performs procurement and sourcing functions which may include but are not limited to short and long-term category strategy development, supplier development and innovation enablement, commodity/services/goods procurement, outsourcing and vendor selection as well as project material sourcing/ planning/scheduling. Creates efficient integrated processes among internal functions and outside suppliers providing an efficient and transparent internal customer experience, compliant with quality assurance and sustainability requirements. Focuses resources on continuous improvement of the movement of materials through various processes and establishes key performance metrics and benchmarks to measure...

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

- Develop, configure, and implement software for PLC, DCS, and SCADA systems across various automation platforms; - Translate functional design specifications into reliable and maintainable automation code; - Troubleshoot and resolve software issues during project execution and post-implementation support phases;

- Build and maintain strong, long-term relationships with senior decision-makers and key influencers within a designated portfolio of customer accounts, which may include major strategic clients in specific geographic or industry sectors -

Responsibility over the development, scale-up, registration/validation of drug substance, particle engineering and drug development programs in compliance with legislation and regulatory standards of Quality, HSE and cGMP policies. Oversees the manufacturing process for clinical or commercial supplies of materials in cooperation with areas and supports safety/hazard analysis and other technical support areas as required. Promotes the scientific excellence and innovation in the area and contributes with technical expertise to expand the Intellectual Property, product and technology portfolios.  

- 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.