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Hovione

CDMO for complex drug APIs manufacturing

Associate Analytical Scientist

Bioprocess & BiomanufacturingConfirmed live in the last 24 hours
Full-timeEast Windsor, NJ, USAIn-person

About the Job

Requirements

  • A university or equivalent qualification in Chemistry, Chemical Engineering, Pharmaceutical Sciences, or a similar Chemistry, Biochemistry, or Health Sciences field is mandatory.
  • Educational or training experience in Analytical Chemistry is required.
  • Basic knowledge of Analytical Chemistry is required.
  • Fluency in English is required.
  • Computer literacy and a 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 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 properties, and control data quality and accuracy in compliance with legislation and Quality, HSE, and cGMP regulatory standards.
  • Promote scientific excellence and innovation in the Analytical area and contribute technical expertise to expand intellectual property, product, and technology portfolios.
  • Assist analytical chemists with analytical laboratory tasks for projects.
  • Perform project analytical tasks, including method development, method and specification creation, method transfer, and preparation of protocols and reports for raw materials, intermediates, and finished products.
  • Contribute to investigations related to analytical activities and help identify Corrective and Preventive Actions (CAPA).
  • Discuss technical project issues within the role's scope with customers, under the guidance of more senior colleagues or line managers.
  • Support client visits under the guidance of more senior colleagues.
  • Review analytical data generated by the team.
  • Apply and develop knowledge of Analytical Chemistry and participate in area processes, procedures, and projects under the guidance of more senior colleagues.
  • Deliver assigned tasks on time, safely, efficiently, reliably, and cost-effectively.
  • Perform professional activities in compliance with Good Manufacturing Practice (GMP) and Health, Safety, and Environment (HSE) guidelines, internal and external requirements, and company policies, systems, and procedures, including COPs, HBR, and SOPs.
  • Carry out assigned tasks safely and in accordance with instructions, environmental, health, and safety rules and procedures, regulations, and codes of practice.

Desired Qualifications

  • Experience in equipment qualification and maintenance 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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