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Hovione

CDMO for complex drug APIs manufacturing

Quality Assurance Trainee

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

About the Job

Requirements

  • A university or equivalent qualification in Chemistry, Chemical Engineering, Pharmaceutical Sciences, or a similar scientific field is mandatory.
  • Fluency in English is required.
  • Computer literacy and good working knowledge of the Microsoft Office package are required.
  • Good documentation skills and attention to detail are required.
  • The candidate must have the knowledge, experience, and skills to conduct tasks in accordance with the applicable rules and procedures.

Responsibilities

  • Support quality activities for assigned projects and products while learning compliance with current Good Manufacturing Practice, operational standards, and legal regulations.
  • Assist in promoting high-quality standards and a culture of continuous improvement across company processes.
  • Help with audits and inspections by preparing documentation and reviewing procedures to ensure the site remains audit ready.
  • Participate in the management of change control, deviations, validation, and other quality-related processes.
  • Learn to prepare, review, and update quality documentation, such as standard operating procedures, reports, and regulatory files.
  • Support investigations related to customer complaints and compliance challenges, collaborating with stakeholders.
  • Assist with data reporting, including key performance indicators and information system updates, while developing expertise in Quality Assurance.
  • Maintain a presence in manufacturing areas, providing on-the-job support and oversight.
  • Ensure compliance with Health, Safety, and Environment regulations in all assigned activities.
  • Guarantee current Good Manufacturing Practice compliance in activities and systems related to project and product execution.
  • Ensure working practices are streamlined and aligned with the actual needs of each project.
  • Implement policies, procedures, and methods to evaluate and continuously improve product and operational quality throughout the product lifecycle.
  • Provide global supplier qualification services in support of new product introduction and existing products.
  • Collaborate with suppliers and Procurement to assure the quality of their products, materials, components, and/or operations.

Desired Qualifications

  • Educational or training experience in a Quality Assurance current Good Manufacturing Practice environment within the pharmaceutical industry is desirable.
  • Experience working in a current Good Manufacturing Practice operational environment is desirable.

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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