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Hovione

CDMO for complex drug APIs manufacturing

Associate Analyst

Inspection & TestPosted on Nov 10
ContractLoures, PortugalNo salary listedIn-person

About the Job

Requirements

  • A high school diploma is mandatory.
  • A qualification in a relevant chemistry, analytical chemistry, chemical engineering, pharmaceutical-related, or other science-related field is mandatory.
  • Relevant work experience is required.
  • Practical pharmaceutical or related-industry experience in a GMP-regulated quality-control laboratory environment is mandatory.
  • Technical understanding of GMP practices, analytical theory, and analytical techniques is required.
  • Availability to work shifts is required.

Responsibilities

  • Define and implement quality-control techniques to verify the quality of raw materials, intermediates, end products, and other analytical services, in accordance with regulatory requirements.
  • Manage and control quality-control activities in accordance with quality-assurance standards, company procedures, client specifications, contract requirements, and regulatory guidelines.
  • Organize daily tasks to ensure efficient execution of sample analysis according to key performance indicators and laboratory schedules.
  • Maintain adherence to good manufacturing practice, health, safety, and environmental regulations, and industry standards in analytical activities.
  • Accurately record information in checklists, laboratory records, and notebooks, following good manufacturing practice and internal procedures.
  • Perform routine equipment calibration and maintenance while ensuring hygienic laboratory conditions.
  • Report discrepancies, investigate atypical results, and support resolution of deviations and quality-control incidents.
  • Collaborate with internal departments using relevant information-technology platforms for quality-control processes.
  • Assist in audits and ensure compliance with internal procedures under quality-control management guidance.
  • Seek additional information when needed, complete self-assessments, and contribute to annual performance reviews.
  • Adhere to good manufacturing practice, health, safety, and environmental requirements, and legal regulations while maintaining high standards in laboratory operations.
  • Undertake additional tasks as required and promote safe, efficient laboratory practices.

Desired Qualifications

  • Experience with good manufacturing practice and health, safety, and environmental standards is preferred.
  • Competent written and verbal English is preferred at sites where English is not the first language.

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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