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Hovione

CDMO for complex drug APIs manufacturing

Analytical Team Lead

Bioprocess & Biomanufacturing +1Posted on Nov 5
Full-timeLisbon, PortugalNo salary listedIn-person

About the Job

Requirements

  • A degree in Chemistry, Chemical Engineering, Pharmaceutical Sciences, or similar Chemistry, Biochemistry, or Health Sciences fields, or equivalent job experience.
  • Relevant experience in Analytical Development or another relevant area within the pharmaceutical industry.
  • Knowledge and experience in HSEE practices.
  • Solid knowledge of Analytical Chemistry or Analytical Development and associated laboratory practices, and the ability to share that knowledge with others.
  • Ability to run work processes and related tools.
  • Ability 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 product.
  • Recommend the analytical characterization package covering chemical, physical, and performance characteristics, 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.
  • Ensure information flows between the laboratory and internal and external customers.
  • Review and approve analytical data generated by the team.
  • Prepare reports and other official documentation based on analytical data.
  • Support project teams in solving and troubleshooting technical and analytical challenges in the relevant area of expertise.
  • Establish and maintain a continuous improvement plan.
  • Participate in investigations and propose corrective and preventive actions.
  • Ensure equipment is verified and calibrated according to established procedures.
  • Ensure the team generates data only using equipment that is in service and properly verified or calibrated according to established procedures.
  • Supervise team members assigned to the area of responsibility and distribute work tasks.
  • Provide input to ensure human resources processes run smoothly, including recruitment, integration, training needs, and performance management in accordance with company policies.
  • Align and motivate team members toward company goals, values, and culture by promoting their personal and professional development while maximizing productivity.
  • Ensure area goals are properly cascaded to the team.
  • Ensure compliance with GMP and HSE guidelines and internal and external requirements, and promote implementation and maintenance of company policies, systems, and procedures, including COPs, HBR, and SOPs, within the team.
  • Carry out assigned tasks safely, following instructions and environmental, health, and safety rules, procedures, regulations, and codes of practice.

Desired Qualifications

  • Knowledge and experience in cGMP.
  • Experience coordinating others in the field.
  • Fluency in English.

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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