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Hovione

CDMO for complex drug APIs manufacturing

Analytical Scientist

Bioprocess & BiomanufacturingConfirmed live in the last 24 hours
Full-timeLisbon, PortugalNo salary listedIn-person

About the Job

Requirements

  • A university or equivalent qualification in Chemistry, Chemical Engineering, Pharmaceutical Sciences, or similar Chemistry, Biochemistry, or Health Sciences fields is mandatory.
  • Typically, 3–5 years of relevant experience in Analytical Chemistry and/or a scientific background in a relevant field; a PhD is considered relevant experience.
  • A strong understanding and knowledge of scientific domains relevant to the pharmaceutical industry is required.
  • Fluency in English is required.
  • Computer literacy and good working knowledge of the Microsoft Office package are required.
  • The candidate must have the knowledge, experience, and skills to conduct tasks in accordance with the rules and procedures established.

Responsibilities

  • Perform qualitative and quantitative analyses of compounds, including drug substances, drug product intermediates, and drug products.
  • Recommend analytical characterization packages covering chemical, physical, and performance characteristics, and control data quality and accuracy in compliance with legislation and regulatory standards, Quality, HSE, and cGMP policies.
  • Promote scientific excellence and innovation in the Analytical area and contribute technical expertise to expand intellectual property, product, and technology portfolios.
  • Perform and support the development of analytical methods and implement innovative and new analytical methodologies.
  • Coordinate priorities with the Area responsible and Project manager to meet project timelines for analytical work, including method development, validation protocols, validation execution, and validation reports.
  • Prepare and revise analytical reports and protocols.
  • Participate in investigations and propose corrective and preventive actions (CAPA).
  • Discuss technical and scientific project issues with customers for work within the role's scope.
  • Support client visits.
  • Discuss and review analytical data generated by the team.
  • Provide internal training and training to other areas as required.
  • Plan and deliver assigned tasks on time, safely, efficiently, reliably, and cost-effectively.
  • Propose area improvements and solve problems.
  • Make quality and timely decisions on analytical tasks under the role's responsibility.
  • Gather relevant data to inform decision-makers on complex issues.
  • Perform professional activities in compliance with GMP and HSE guidelines and internal and external requirements, and promote implementation and maintenance of company policies, systems, and procedures, including COPs, HBR, and SOPs.
  • Carry out assigned duties safely, following instructions and environmental, health, and safety rules, procedures, regulations, and codes of practice.

Desired Qualifications

  • A PhD in Chemistry, Chemical Engineering, Pharmaceutical Sciences, or similar Chemistry, Biochemistry, or Health Sciences fields is desired.
  • Experience in the pharmaceutical industry 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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