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 and technology 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?
Responsibilities
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) 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.
Coordinate the implementation of new procedures or the change of existing ones, according to ruling COPs and SOPs.
Enforce fulfillment of the GMP and HSE policy, by supporting inspections and liaising with other Areas.
Ensure HSE operational program targets accomplishment.
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 and procedures.
Prepare manufacturing plans for production lines, managing resources allocation and assigning the members responsible (when applicable) for specific tasks.
Qualifications
Degree in a field of Science or Engineering (with a preference in Chemical Engineering)
Experience working within the pharmaceutical industry in Pharmaceutical Fine Chemistry and/or Particle Engineering and/or Drug Product (areas of development, scale‑up and production) (mandatory)
Training and experience in GMP and HSE practices (mandatory)
Experience in equipment and technology design (mandatory)
Experience in technical manufacturing support
Experience of technical transfer and capital project support
Experience of multiple projects and product from early stage development to commercial scale
Strong interpersonal skills to enable effective interactions with stakeholders (written and verbal)
Competent (written and verbal) English
Computer literate with good working knowledge of the MS Office package and SAP
Advanced knowledge in organic chemistry and/or particle engineering technologies
Advanced knowledge in scale‑up of chemical engineering operations and/or drug product
Expertise or significant experience in other departments or areas in a Pharmaceutical organization such as Quality Assurance, Analytical Development, Quality Control, Project Management, Process R&D, from completed assignments or past job experience (preferable)
Must have the Knowledge, Experience and Skills to conduct their tasks in accordance with the rules and procedures set down.
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 résumes 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. Thank you for your understanding.
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