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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.
- Rigorously, efficiently and professionally, execute all production/HSE...
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Purpose of the Role
Enable the efficient manufacture of pharmaceutical products, including highly potent compounds, while ensuring full compliance with cGMP and HSE requirements. The role is responsible for defining, implementing, improving, and supporting manufacturing processes and systems to deliver products safely, on time, within budget, and according to customer and business requirements.
Manufacturing Process Management
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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)...
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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 all applicable current Good Manufacturing Practices (cGMP) and Health...
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Ensure efficient and compliant manufacturing of pharmaceutical products, including highly potent compounds, following cGMP, HSE, and business requirements;
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Organize, execute, and autonomously perform production activities according to procedures, instructions, and established schedules;
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Complete, maintain, and ensure accuracy of all required production documentation and equipment...
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Oversee and supervise all production activities to ensure efficient, safe, and right‑first‑time operations aligned with cGMP, HSE, and business requirements;
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Promote a strong safety and quality culture by identifying risks, implementing mitigation actions, and ensuring compliance with all regulations and standards;
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Drive continuous improvement by proposing and implementing optimizations in...
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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...
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- 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;
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