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Hovione

CDMO for complex drug APIs manufacturing

Analytical Manager

Bioprocess & Biomanufacturing +1Confirmed live in the last 24 hours
Full-timeLisbon, PortugalNo salary listedIn-person

About the Job

Requirements

  • A master's degree in Chemistry, Chemical Engineering, Pharmaceutical Sciences, or a similar Chemistry, Biochemistry, or Health Sciences field is required.
  • Typically, five years of relevant experience in analytical development or another relevant area within the pharmaceutical industry is required; a PhD counts as relevant experience.
  • Effective time management skills and the ability to adapt to changes are required.
  • A track record of overachieving targets is required.
  • Knowledge and experience in HSEE practices are mandatory.
  • Solid knowledge of Analytical Chemistry, development and validation of analytical methods, and quality control principles and practices is required.
  • Good verbal and written communication skills are required.
  • Skill in managing processes and tools is required.
  • Fluency in English is 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 attributes, and control the quality and accuracy of data 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.
  • Evaluate material and human resource needs for analytical projects to ensure timely and appropriate analytical support for customers.
  • Manage proposals for alternatives to project analytical packages.
  • Support implementation of new and state-of-the-art analytical methodologies.
  • Review and approve laboratory analytical test methods, protocols, reports, and documentation prepared in the Area or provided by customers.
  • Ensure information flows between the laboratory and internal and external customers.
  • Support analytical development activities and investigations, providing guidance and technical analytical consultancy to teams across the organization, particularly in problem solving.
  • Monitor group performance and implement measures to increase productivity continuously.
  • Promote scientific excellence and innovation within the team and support implementation of new technologies and methodologies.
  • Contribute to proposals for Exploration and Investment budgets.
  • Coordinate assigned team members, including recruitment, integration, training needs, and performance management in accordance with company HR policies; support their development and productivity.
  • Develop and propose for superior approval the Area activity plan and related budget in line with unit strategy and department strategic objectives.
  • Ensure compliance with GMP and HSE guidelines and internal and external requirements, and promote implementation and maintenance of company policies, systems, and procedures within the team.
  • Carry out assigned tasks and duties safely and in accordance with instructions, environmental, health and safety rules and procedures, regulations, and codes of practice.

Desired Qualifications

  • A technical background is preferred.
  • Experience leading others in a project context is desired.
  • Knowledge and experience in cGMP are 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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