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Enables the efficient manufacture of pharmaceutical products, including highly potent compounds, in compliance with applicable cGMP and HSE regulations and in accordance with business requirements. Responsible for the definition, implementation and optimization of manufacturing processes and systems, aiming at full adherence to pre-established schedules while managing internal resources (people & equipment) and fulfilling costumer requirements.   - Fulfill and rigorously promote all applicable Good Manufacturing Practices (GMP)...

Assegurar o fabrico eficiente de produtos farmacêuticos, incluindo compostos altamente potentes, em conformidade com os regulamentos de Boas Práticas de Fabrico (GMP) e de Higiene, Segurança e Ambiente (HSE) aplicáveis e de acordo com os requisitos do negócio.   Executar, de forma rigorosa, eficiente e profissional, todas as atividades de produção/HSE, cumprindo todos os procedimentos aplicáveis e seguindo as instruções recebidas de superiores hierárquicos. · Executar, sob supervisão, os processos de produção/HSE.

Enables the efficient manufacture of pharmaceutical products, including highly potent compounds, in compliance with applicable cGMP and HSE regulations and in accordance with business requirements. Responsible for the definition, implementation and optimization of manufacturing processes and systems, aiming at full adherence to pre-established schedules while managing internal resources (people & equipment) and fulfilling costumer requirements.   - Fulfill all applicable current Good Manufacturing Practices (cGMP) and Health...

- Conduct Impact Assessments and Risk Assessments for new or modified systems; - Draft User Requirements Specifications (URS) to support project and compliance needs; - Contribute to Enhanced Design Reviews, ensuring alignment with technical and regulatory standards; -

Delivers excellence in end-to-end process improvement practices, methodologies and behaviours to achieve transversally operational and support services areas’ efficiencies. Demonstrates particular leadership skills to influence the right behaviours and enable alignment of priorities across areas. Supports the continuous improvement cycle aiming at the sustainable increase of unitary output (effective throughput per resource unit used). Responsible for developing, deploying and maintaining the most adequate methodologies and workflows, looking at maximization of workforce efficiency and adoption of the appropriate behaviours to enable engagement; as well as for deriving metrics...

- Fulfill all applicable current Good Manufacturing Practices (cGMP) and Health Safety and Environment (HSE) regulations and relevant legislation by adhering to Hovione´s policies and procedures (COPs, HBR, SOPs and others) and industry standards while conducting all activities; - Plan and design manufacturing processes that ensure the production of intermediates and final products according to the project plan (reliably, right first time, on time and within budget) and in compliance with cGMP, HSE regulations and internal policies and procedures; -

- Support and mentor production teams to optimize drug product manufacturing processes, minimize downtime, and maximize productivity; - Identify and troubleshoot operational issues related to equipment and drug product processes, implementing innovative solutions to enhance efficiency and quality; - Monitor and analyze production data to ensure compliance with regulatory standards and quality control measures; -

Enables the efficient manufacture of pharmaceutical products, including highly potent compounds, in compliance with applicable cGMP and HSE regulations and in accordance with business requirements. Responsible for the definition, implementation and optimization of manufacturing processes and systems, aiming at full adherence to pre-established schedules while managing internal resources (people & equipment) and fulfilling costumer requirements.   - Fulfill and rigorously promote all applicable Good Manufacturing Practices (GMP) and Health Safety and...