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- Learn and provide support to the principle HR technical resource for a variety of HR systems including troubleshooting, configuration, and support; - Execute test scripts to ensure seamless configuration changes and updates; - Support the implementation of improvements in process through enabling systems; -

- 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...

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.

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.  

Defines and implements quality control techniques in order to verify the quality of raw materials, intermediate and end products as well as any other analytical services relevant to our client base and according to regulatory requirements. Manage and control all Quality Control activities in accordance with identified quality assurance standards, company procedures, client specifications, contract requirements, and regulatory guidelines.   - Follow the daily priorities in order to accurately and promptly perform the allocated...

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.   - Evaluate...

We are seeking an experienced procurement professional to lead the strategic and operational management of our company car fleet, corporate travel and on site facilities categories. This role is responsible for delivering cost-effective, compliant, and sustainable mobility solutions aligned with business needs and corporate standards. Key Responsibilities - Develop and implement category strategies for company fleet, corporate...

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...

Defines and implements quality control techniques in order to verify the quality of raw materials, intermediate and end products as well as any other analytical services relevant to our client base and according to regulatory requirements. Manage and control all Quality Control activities in accordance with identified quality assurance standards, company procedures, client specifications, contract requirements, and regulatory guidelines.   -

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.  

Defines and implements procedures and processes to assure that Hovione facilities, equipment and supporting systems are fit for purpose and comply with applicable quality standards, documenting evidence that these can perform effectively and reproducibly to meet predetermined specifications and quality attributes to manufacture a product when operated within established parameters. Works collaboratively with colleagues to support the design of test strategies and methodologies for qualification and validation application, by developing and deploying Best Practices.   - Assure cGMP...

Defines and implements quality control techniques in order to verify the quality of raw materials, intermediate and end products as well as any other analytical services relevant to our client base and according to regulatory requirements. Manage and control all Quality Control activities in accordance with identified quality assurance standards, company procedures, client specifications, contract requirements, and regulatory guidelines.   - To organize and define daily priorities within their assigned tasks in order to accurately...

In this position, you will apply and further develop quality control techniques to ensure that raw materials, intermediate products, and finished products meet the highest quality standards. You will also provide essential analytical services to our clients, always in compliance with the relevant regulatory requirements. You will be responsible for coordinating and overseeing all Quality Control activities, ensuring they align with quality assurance standards, internal procedures, client specifications, contractual requirements, and regulatory...

Defines and implements quality control techniques in order to verify the quality of raw materials, intermediate and end products as well as any other analytical services relevant to our client base and according to regulatory requirements. Manage and control all Quality Control activities in accordance with identified quality assurance standards, company procedures, client specifications, contract requirements, and regulatory guidelines.   - To organize and define daily priorities within their assigned tasks in order to accurately...

- Partner with stakeholders across functions as a data business partner, identifying high impact use cases and areas for improvement;  - Build, standardize, and maintain reporting and self-service analytics as part of data centralization (incl. data lake concepts);  - Preprocess and engineer features from structured and unstructured data, ensuring quality, lineage, and...

- 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; -

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.  

- Lead the implementation of HSE & Sustainability management systems, policies, procedures, and standards across the site, ensuring alignment with applicable laws and corporate requirements (incl. ISO 14001 & ISO 45001);  - Plan and perform risk assessments (e.g., Chemical Risk Assessment, Task Risk Assessment, PHA) and participate in HAZOP studies; define, track, and verify mitigation plans;  -

The HSE Global Compliance Director is a senior, independent oversight role responsible for establishing, governing, and continuously strengthening Hovione’s global Health, Safety & Environmental (HSE) compliance systems.  As the HSE Global Compliance Director you will ensure that all sites operate in full adherence to applicable regulations, internal standards, and major accident hazard prevention requirements—regardless of operational constraints or local decision‑making considerations. As a key member of the Global HSE Leadership Team, the...