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Hovione

CDMO for complex drug APIs manufacturing

Analyst

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

About the Job

Requirements

  • A bachelor's degree in chemistry, analytical chemistry, chemical engineering, a pharmaceutical-related field, or another relevant science.
  • At least three years of practical experience in a GMP-regulated quality control laboratory in the pharmaceutical or a related industry.
  • Extensive hands-on testing experience, including wet chemistry and instrumental techniques such as high-performance liquid chromatography and gas chromatography using Empower software, with the ability to troubleshoot these techniques.
  • Experience performing data review.
  • Technical understanding of good manufacturing practices, analytical theory, and analytical techniques.
  • Clear and open written and verbal communication skills.
  • Computer literacy and working knowledge of Microsoft Office.
  • Knowledge, experience, and skills to carry out tasks in line with established rules and procedures.

Responsibilities

  • Test finished product and stability samples according to the laboratory testing schedule.
  • Perform wet chemistry and instrumental analysis, including high-performance liquid chromatography and gas chromatography, and troubleshoot issues with these techniques.
  • Review analytical data.
  • Maintain all checklists, laboratory records, and notebooks involved in to good manufacturing practice standards and in accordance with internal procedures.
  • Maintain good hygiene and housekeeping in the laboratory.
  • Carry out routine calibration and maintenance of laboratory instruments, and manage the necessary consumables.
  • Identify and report discrepancies, deviations, and non-conformances in testing or laboratory practices.
  • Raise and support investigations into out-of-specification, out-of-trend, atypical results, and other quality control incidents.
  • Collaborate with internal departments using established communication platforms and processes.
  • Support audits and contribute to continuous improvement initiatives.
  • Take on additional tasks to support laboratory activities as required.
  • Comply with all safety, environmental, and good manufacturing practice regulations and standards.

Desired Qualifications

  • Experience with additional techniques such as Karl Fischer analysis, particle size analysis, capillary electrophoresis, or ion chromatography.
  • Knowledge of health, safety, and environmental standards.

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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