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Hovione

CDMO for complex drug APIs manufacturing

Scientist

Bioprocess & BiomanufacturingPosted on Nov 5
Full-timeLisbon, PortugalNo salary listedIn-person

About the Job

Requirements

  • A university degree or equivalent in Chemistry, Chemical Engineering, Materials Sciences, Pharmaceutical Technology, Biological Engineering, Biology, Mechanical Engineering (for devices), or a similar scientific field is mandatory.
  • A PhD in a relevant scientific field is preferred.
  • Typically, 3–5 years of relevant Research & Development and/or Operations experience in the pharmaceutical industry is required, or a PhD in a relevant scientific field.
  • Strong understanding of at least one of the following areas: Chemical Engineering, Chemistry, Organic Chemistry, and Unit Operations; Reaction Engineering, Heat Transfer, Scale-up, Process Safety, and Industrial Operations; drug product unit operations, solids flow phenomena, and process equipment; drug product formulation and drug delivery; or Mechanical Engineering and Fluid Dynamics.
  • Knowledge of mathematics is required; data management, statistics, and first-principles modeling are preferred.
  • Fluency in English is required.
  • Computer literacy and good working knowledge of Microsoft Office are required.
  • Must have the knowledge, experience, and skills to conduct tasks in accordance with established rules and procedures.

Responsibilities

  • Resolve technical challenges across multiple projects to meet established targets.
  • Execute projects according to agreed work plans, selecting optimal methods and techniques.
  • Provide technical support to projects beyond direct responsibility.
  • Present recommendations and contribute to idea generation within cross-functional teams.
  • Generate technical documentation and reports.
  • Contribute to process and procedure improvements.
  • Communicate with clients and stakeholders on project-related topics.
  • Recommend methods and procedures for new or special assignments.
  • Develop new procedures and methodologies based on experience and innovative approaches.
  • Generate intellectual property and promote scientific activities and innovation.
  • Develop personal and others’ technical competencies.
  • Represent Hovione at external events, conferences, and industry forums.
  • Train staff in specialized subjects related to the role’s expertise.
  • Participate in inspections and internal and external audits.
  • Network with internal and external peers beyond the role’s area of expertise.
  • Lead and participate in peer reviews within cross-functional teams and asset groups.
  • Ensure assigned tasks are delivered on time, safely, efficiently, and cost-effectively.
  • Propose improvements and solve problems proactively.
  • Make quality, timely decisions within the scope of responsibility.
  • Gather and analyze relevant data to inform decisions on complex issues.
  • Execute professional activities in compliance with Good Manufacturing Practice, health, safety, and environmental guidelines, and internal and external requirements.
  • Promote and maintain company policies, systems, and procedures.
  • Carry out tasks safely and in compliance with environmental, health, and safety regulations.

Desired Qualifications

  • A solid foundation in mechanical, biomedical, or related engineering disciplines is preferred.
  • Experience in process modelling, simulation, or computational analysis is preferred.
  • Familiarity with injectable drug development, manufacturing processes, or related technologies is preferred.

About the Company

Hovione

CDMO for complex drug APIs manufacturing

Hovione is a contract development and manufacturing organization that creates and scales active pharmaceutical ingredients (APIs) for medicines. It handles complex chemistry and specializes in processes like particle engineering and spray drying to improve drug absorption. It differentiates itself through a long history of tackling difficult compounds, deep manufacturing expertise, and an FDA-inspected global footprint across Portugal, Ireland, China, and the US. Its goal is to help drug developers bring new medicines to market efficiently by providing high-quality, scalable manufacturing and expanding capacity, especially in the U.S.

Company size
1,001-5,000
Company stage
Not listed
Total funding
Not listed
Headquarters
Loures, Portugal
Founded
1959

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