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This is a 2nd shift position - 1:30pm - 10:00pm   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 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...

This is a 2nd shift position: 1:30pm - 10:00pm   Coordinates inbound and outbound logistical operations being accountable for the imports and exports of goods and also information flows supporting these operations. Manages inventory, warehousing operations, regulate warehouse space, including reception, pathway, sampling, dispensing and arrange shipments, and local transportation to ensure an efficient supply of goods. Administers an effective system that meets the organization’s inventory targets through...

As Engineering & Maintenance Manager, you will be responsible for supervising maintenance operations, leading technical teams and contractors, and ensuring the reliable performance of site equipment and utilities. You will drive continuous improvement initiatives, support site growth, and foster a culture of safety, quality, and operational excellence. Maintenance & Technical Leadership - Supervise the timely execution of preventive, corrective, and calibration...

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.  

- Lead the delivery of major engineering and capital projects from concept and feasibility through design, procurement, construction, commissioning and handover. - Develop and execute project strategies, ensuring projects are delivered safely, compliantly, on time and within agreed budgets. - Lead a team of project engineers and technical professionals, providing direction, coaching, development and performance management. - Manage multiple complex...

We are looking for an experienced Senior Automation Engineer to join our Automation team. This is a senior individual contributor role with manager-level accountability, providing technical leadership across automation design, system lifecycle management, validation, troubleshooting, and continuous improvement initiatives. This position offers a unique opportunity to combine operational support, project delivery, digital innovation, and strategic influence within a highly regulated GMP manufacturing environment. Automation...

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)...

- Test finished product and stability samples in line with the laboratory testing schedule. - Perform wet chemistry and instrumental analysis, including HPLC and GC, and troubleshoot issues with these techniques. - Review analytical data. -

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...

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...

This is a 2nd shift position - 1:30pm - 10:00pm   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.

As Senior Maintenance Engineer, you will be responsible for the reliability, performance, and lifecycle management of critical utility systems supporting site operations. Key responsibilities include: - Ensure all plant utilities and facilities operate safely, reliably, and efficiently to support site production requirements. -

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, organize and execute all production...

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, organize and execute all production...

Join a dynamic and highly technical environment where quality, innovation, and continuous improvement are at the heart of everything we do. As a Quality Control Supervisor, you will play a key leadership role in ensuring the delivery of high-quality analytical services while developing people, driving operational excellence, and maintaining the highest standards of compliance and scientific rigor. What You'll Do - Lead and inspire a team of Quality...

Suggests, develops and implements process analytical tools to boost the company efficiency in the areas of Drug Substance, Drug Product Intermediate and Drug Product. Oversees and qualifies the implementation of these tools in the manufacturing assets in compliance with legislation and regulatory standards of Quality, HSE and cGMP policies. Assures modelling practices and methodologies are aligned with the state of the art. Promotes the scientific excellence and innovation in the area of Modelling and PAT and contributes with technical expertise to expand the Intellectual Property, product and technology portfolios.

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.  

Act as the company's Subject Matter Expert (SME) for:   - Process Validation - Cleaning Validation - Contamination Control Strategy - New Product Introduction - Regulatory segregation requirements for the manufacture and handling of highly active, potent, toxic, sensitizing, and other special-category compounds   You will also be Responsible to: - Promote the importance of high-quality work levels and the importance of a continuous improvement culture in all Quality and/or Regulatory Systems activities - Open and maintain active and efficient communication channels along the several...