Ready to make better happen?

Contribute to impactful projects across a dynamic, global organisation while developing the skills and experience needed to become part of our future leadership and technical expert talent pool. Working alongside experienced professionals, you will gain hands-on exposure across multiple disciplines and functions in a collaborative, innovation-driven environment spanning Portugal, the USA, Ireland, and China.   What’s in...

- Lead Commissioning, Qualification and Validation (CQV) activities for facilities, equipment, utilities, and systems in compliance with GMP and regulatory requirements. - Develop and execute CQV strategies, including DQ, IQ, OQ, and PQ, ensuring validation readiness and successful project...

Ensure full compliance with cGMP, GDP, and regulatory requirements across product lifecycle activities, acting as the ultimate authority for batch certification and release. Drive a strong quality culture, safeguard patient safety, and enable business continuity through effective quality oversight and decision-making. Quality & Compliance Leadership •    Ensure compliance with GMP,...

Ensure full compliance with cGMP, GDP, and regulatory requirements across product lifecycle activities, acting as the ultimate authority for batch certification and release. Drive a strong quality culture, safeguard patient safety, and enable business continuity through effective quality oversight and decision-making. Quality & Compliance Leadership •    Ensure compliance with GMP,...

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. -

- Identify and survey critical instrumentation assets (flow meters, thermometers, pressure and temperature transmitters, etc.) across the plant for which spare parts are currently unavailable. - Codify identified instruments within the plant's asset management framework, ensuring full...

- 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; -

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...

- 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...

- Lead in‑depth analysis of pharmaceutical markets, competitors, technologies, and customer dynamics. - Anticipate external trends and strategic risks, assessing their implications for long‑term business direction. - Leverage advanced analytics and emerging technologies (including AI) to synthesize complex intelligence from diverse sources. - Translate sophisticated analyses into clear, actionable insights tailored to senior and functional...

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.  

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)...

- Ensure cGMP, HSE and engineering best practices are embedded from the URS stage through detailed design; - Lead and execute construction, assembly, commissioning and qualification activities for...

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.   -

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...

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 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...

- 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; -