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Hovione

CDMO for complex drug APIs manufacturing

Senior Design Engineer

Design EngineeringPosted on Nov 9
Full-timeLisbon, PortugalNo salary listedIn-person

About the Job

Requirements

  • A university degree or equivalent qualification in Engineering, preferably in Mechanical, Chemical, Electrical, or Instrumentation Engineering, is mandatory.
  • Experience in operational environments and execution of significant industrial projects is mandatory.
  • Experience in project management.
  • Knowledge of current Good Manufacturing Practice (cGMP) guidelines, health, safety and environmental (HSE) standards, Good Engineering Practices (GEP), and applicable legal requirements for the specialty of focus.
  • Fluency in English.
  • Computer literacy and good working knowledge of the Microsoft Office package.

Responsibilities

  • Plan and design manufacturing facilities and related structures, determine facility specifications, and evaluate locations, material resources, and structural design.
  • Resolve technical problems and recommend installation improvements to meet process requirements.
  • Participate in defining user requirements specifications (URS), understand and support user needs, and contribute to specifications fit for intended use while promoting user wellbeing, ergonomics, and productivity.
  • Conceive, design, and implement engineering solutions in specific areas of complex engineering projects to achieve company objectives and successful project conclusions.
  • Master the technical solutions for conceptual, basic, and detailed design of complex new installations or modifications to existing installations, incorporating company Engineering standards and state-of-the-art solutions.
  • Prepare, revise, and approve technical documentation for Engineering Projects across conceptual, basic, and detailed design phases.
  • Ensure project documents are complete and optimized for a competitive tender process.
  • Assess and manage project risks to ensure installations and equipment comply with regulatory and legal requirements while optimizing the quality-cost ratio.
  • Execute assigned tasks by planning and delivering them on time, safely, efficiently, reliably, and cost-effectively.
  • Work with other Engineering areas and project management to resolve project issues and ensure project work is delivered and completed.
  • Propose appropriate improvements in Engineering, including procedures, organization, technologies, capital expenditure, and productivity.
  • Manage risk and uncertainty, and anticipate and escalate roadblocks to prevent deviations from goals.
  • Perform professional activities in compliance with Good Manufacturing Practice (GMP) and internal and external requirements, and promote implementation and maintenance of company policies, systems, and procedures, including COPs, HBR, and SOPs.
  • Support other team members on matters related to Design Engineering processes and tools.
  • Update the area Director on relevant occurrences and trends that may significantly impact the business.

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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