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Hovione

CDMO for complex drug APIs manufacturing

Senior Analytical Scientist

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Full-timeLisbon, PortugalNo salary listedIn-person

About the Job

Requirements

  • A PhD qualification in Chemistry, Chemical Engineering, Pharmaceutical Sciences, or similar Chemistry, Biochemistry, or Health Sciences fields is mandatory.
  • Typically requires 5–8 years of relevant experience in Analytical Chemistry and/or a scientific background in a relevant field; a PhD is considered relevant experience.
  • Advanced understanding and knowledge of scientific domains relevant to the pharmaceutical industry, with the ability to solve complex problems.
  • Fluency in English is required.
  • Computer literacy and good working knowledge of the Microsoft Office package.
  • Knowledge, experience, and skills to conduct tasks in accordance with established rules and procedures.

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 attributes, 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 analytical tasks for complex projects, including method development, method and specification creation, method transfer, and preparation of protocols and reports.
  • Support others with identical activities.
  • Solve complex project analytical problems.
  • Determine the work and effort required to accomplish a scope of work and propose solutions that meet and exceed client expectations.
  • Discuss technical and scientific issues actively with customers.
  • Supervise the activities of less experienced colleagues in the work group.
  • Prepare and discuss complex product specifications.
  • Conduct and supervise analytical investigations and contribute to defining and implementing corrective actions.
  • Support audits and client visits.
  • Evaluate and approve materials and supplier qualifications.
  • Provide training internally and to other areas as required.
  • Master Analytical Chemistry processes and tools.
  • Manage complex projects and analyses with significant business impact.
  • Make quality and timely decisions based on multiple sources of data.
  • Manage risk and uncertainty, and anticipate and escalate roadblocks to prevent deviations from goals.
  • Execute professional activities in compliance with GMP and HSE guidelines, internal and external requirements, and promote implementation and maintenance of company policies, systems, and procedures.
  • Carry out assigned tasks safely, following instructions and applicable environmental, health, and safety rules, procedures, regulations, and codes of practice.

Desired Qualifications

  • Relevant 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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