Analytical Manager

en-careers-hovione; Lisboa; Presencial; EUR 55 000 - 75 000; Tempo integral

Resumo da oferta

Hovione in Portugal is seeking an experienced Analytical Development professional to lead qualitative and quantitative analyses of drug substances and products. You will define analytical characterization packages, ensure data quality, and support GMP/HSE compliance across the lab and with customers.

The ideal candidate holds a Master’s in Chemistry or related field, has about 5 years in analytical development in pharma, and can lead teams, communicate effectively in English, and drive

Qualificações

• Master's degree in Chemistry or related field required.
• Typically requires 5 years of relevant experience in analytical development.
• Experience in leading others in project context desirable.
• Knowledge of cGMP and HSEE practices recommended.

Responsabilidades

• Evaluate needs of material and human resources for analytical projects to provide timely support.
• Manage proposals of alternatives to analytical packages for projects.
• Support implementation of new analytical methodologies and technologies.
• Review and approve analytical methods, protocols, and reports.
• Ensure information flow between the lab and internal/external customers.
• Provide technical analytical consultancy to teams across the organization.

Conhecimentos

Leadership experience

Time management

Communication skills

English fluency

GMP/HSE knowledge

Analytical chemistry expertise

Formação académica

Master's degree in Chemistry or related field

Descrição da oferta de emprego

Join a Market Leader

About Hovione

At Hovione, we help partners turn scientific innovation into medicines that reach patients around the world. For more than 65 years, we have connected science, technology, and manufacturing to scale complex ideas into high-quality and innovative solutions that truly make a difference.

As an international Contract Development and Manufacturing Organization (CDMO), we support the development and manufacture of drug substances, intermediates, and drug products across the full life cycle. We are globally recognized for our leadership in specialized technologies such as Spray Drying and Continuous Tableting. But what truly sets us apart is not just what we do — it is how we do it: with purpose, care, collaboration, and a deep commitment to doing the right things right.

Our people are the reason for our success. We are a global and diverse team of more than 2,600 team members across Europe, the USA, and Asia, bringing together different experiences and perspectives to help our partners to overcome complex challenges. We believe that an inclusive environment — where everyone, regardless of background, identity or ability, is respected, heard and empowered to contribute — is essential to drive innovation, ensure quality, and secure long‑term sustainable success.

And as we grow, so do the opportunities for our people to develop, broaden their perspectives, and build meaningful careers. Because at Hovione, better starts with those who choose to make a difference every day. Will you be one of them?

You will be responsible to:

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 the needs of both the material and human resources for the analytical projects to guarantee that the right analytical support is given in time to customers
• Manage the proposals of alternatives to projects analytical packages
• Support the implementation of new and state of the art analytical methodologies
• Review and approve the analytical test methods to be executed in the laboratory and the protocols, reports and documentation prepared in the Area or provided by the customers
• Ensure the information flow between the laboratory and the several internal and external customers
• Support analytical development activities and investigations, providing guidance and technical analytical consultancy to teams across the organization, particularly in the problem solving process
• Monitor the performance of the group, implementing the necessary measurements for continuous productivity increase
• Promote scientific excellence and innovation within the team and support in the implementation of new technologies/methodologies
• Contribute to the proposal of the Exploration and Investment budgets
• Coordinate the TMs assigned to his/her area of responsibility, namely in terms of recruitment, integration, training needs and performance management in accordance with the company's HR policies, in order to ensure all TMs are aligned and motivated towards achieving Hovione's goals, values and culture by promoting their personal and professional development whilst maximizing productivity
• Develop and propose for superior approval the activity plan and related budget for the Area under responsibility in line with the unit's strategy, in order to align activities with DEPARTMENT strategic objectives
• Ensure compliance with GMP and HSE guidelines, internal and external requirements as well as promote the implementation and maintenance of Hovione´s policies, systems and procedures (COPs, HBR, SOPs and others) within his/ her TMs
• Carry out assigned tasks and duties in a safe manner, in accordance with instructions, and to comply with environmental, health & safety rules/procedures, regulations and codes of practice

We are looking to recruit a Candidate:

• Masters degree in Chemistry, Chemical Engineering, Pharmaceutical Sciences or in similar Chemistry/ Biochemistry/ Health Sciences fields
• Technical background preferred
• Typically requires 5 years of relevant experience in analytical development or other relevant areas within the Pharmaceutical industry (PhD counts as relevant experience)
• Experience in leading others in project context (desired)
• Effective time management skills and ability to adapt to changes
• Track record of overachieving targets
• Knowledge and Experience in cGMP (desirable) and HSEE practices (mandatory)
• Possess solid knowledge of Analytical Chemistry, Development and Validation of analytical methods and QC principles and practices
• Good communication skills (verbal and written)
• Skilled at managing processes and tools
• Fluency in English is a requirement
• Must have the Knowledge, Experience and Skills to conduct their tasks in accordance with the rules and procedures set down

Hovione is a proud Equal Opportunity Employer

Inclusion and diversity are key to us. We are committed to creating an inclusive recruitment experience and welcome applications from all qualified candidates. If you require any reasonable accommodation or support during the application or interview process, please contact us, and we will be happy to assist.