R&D Manager

en-careers-hovione; Lisboa; Presencial; EUR 85 000 - 115 000; Tempo integral

Resumo da oferta

Hovione is a leading CDMO seeking a senior candidate to lead development, scale-up, and validation of drug substances and formulation processes. The role emphasizes regulatory compliance, quality systems, and innovation across programs.

The successful applicant will drive strategy, manage resources and budgets, and mentor teams while collaborating with cross-functional partners to deliver high-quality medicines. Proficiency in English is required.

Qualificações

• Masters' degree in Chemistry, Engineering, Materials Sciences, Pharmaceutical Technology, or related field.
• -Fluency in English is required.
• -Typically requires 5 years of relevant experience in R&D and/or Operations in the Pharmaceutical Industry.
• -Experience in leading others in a project context.
• -Solid knowledge of chemical engineering topics and unit operations.

Responsabilidades

• Oversee development, scale-up, registration/validation of drug substances and particle engineering.
• Manage the manufacturing process for clinical or commercial supplies with GMP/HSE compliance.
• Promote scientific excellence and expand IP, products, and tech portfolios.
• Assess resources needs and ensure timely scientific support for projects.
• Supervise projects, allocate resources, and meet deliverables on time.
• Coordinate recruitment, training, and performance within the team.

Conhecimentos

Leadership

Communication

Time management

Project management

English fluency

Chemical engineering

Organic chemistry

Unit operations

Formação académica

Masters degree

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:

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.

• Evaluate the needs of both the material and human resources for the area’s projects to guarantee that the right scientific support is given in time to customers
• Supervise all projects within his/her Group, ensures that execution is flawless and that adequate resources are allocated to meet the project goals and all deliverables are met in time for invoicing
• Define a development and validation strategy for new projects and establish the scientific and research plan within his/her Group
• Support the implementation of new and state of the art methodologies and/or equipment
• Review and approve the technical reports and documentation prepared in the Area
• Ensure the information flow between the laboratory and the several internal and external customers
• Support development activities and investigations, providing guidance and technical consultancy to teams across the organization, particularly in the problem solving process once escalation occurrs
• 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
• 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 area strategic objectives
• Monitor Communication´s budget, by controlling budget evolution, identifying any deviations between the real and the foreseen and taking corrective measures
• 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, Engineering, Materials Sciences, Pharmaceutical - Technology, or related field
• Technical background preferred
• Typically requires 5 years of relevant experience in Research & Development and/or Operations in the Pharmaceutical Industry
• Experience in leading others in project context
• Effective time management skills and the ability to multitask.
• Track record of overachieving targets
• Possess solid knowledge of Chemical Engineering, Chemistry, Organic Chemistry and Unit Operations, or of Reaction Engineering, Heat Transfer, Scale-up, Process Safety and Industrial Operations, or of drug product unit operations, solids flow phenomena and process equipment 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.

Notice to Agencies and Search Firms Representatives

Hovione does not accept unsolicited resumes from agencies or search firms for this job posting. Any resumes submitted to Hovione by a third-party agency or search firm without a valid written and signed search agreement will become the sole property of Hovione. No fees will be paid if a candidate is hired for this position as a result of an unsolicited referral.