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Hovione

CDMO for complex drug APIs manufacturing

R&D Manager

Bioprocess & BiomanufacturingConfirmed live in the last 24 hours
Full-timeLisbon, PortugalNo salary listedIn-person

About the Job

Requirements

  • A Master's degree in Chemistry, Engineering, Materials Sciences, Pharmaceutical Technology, or a related field is required.
  • A technical background is preferred.
  • Typically, five years of relevant experience in Research & Development and/or Operations in the pharmaceutical industry is required.
  • Experience leading others in a project context is required.
  • Effective time management and the ability to multitask are required.
  • A track record of overachieving targets is required.
  • Knowledge of Chemical Engineering, Chemistry, Organic Chemistry and Unit Operations, or Reaction Engineering, Heat Transfer, Scale-up, Process Safety and Industrial Operations, or drug product unit operations, solids flow phenomena and process equipment 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 knowledge, experience and skills needed to conduct tasks in accordance with established rules and procedures are required.

Responsibilities

  • Oversee development, scale-up, registration and validation of drug substance, particle engineering and drug development programs in compliance with legislation and regulatory standards, Quality, HSE and cGMP policies.
  • Oversee manufacturing processes for clinical or commercial material supplies in cooperation with other areas, and support safety and hazard analysis and other technical support areas as required.
  • Promote scientific excellence and innovation and contribute technical expertise to expand intellectual property, product and technology portfolios.
  • Evaluate material and human resource needs for area projects to ensure appropriate scientific support is provided to customers on time.
  • Supervise all projects within the group, ensure flawless execution, allocate adequate resources, and meet project goals and deliverables on time for invoicing.
  • Define development and validation strategies for new projects and establish the group's scientific and research plans.
  • Support implementation of new methodologies and equipment.
  • Review and approve technical reports and documentation prepared in the area.
  • Ensure information flows between the laboratory and internal and external customers.
  • Support development activities and investigations by providing guidance and technical consultancy to teams across the organization, particularly in problem-solving after escalation.
  • Monitor group performance and implement measures to continually increase productivity.
  • Promote scientific excellence and innovation within the team and support implementation of new technologies and methodologies.
  • Coordinate team members in the area, including recruitment, integration, training needs and performance management in accordance with company HR policies, supporting their development, alignment and productivity.
  • Develop and propose for superior approval the area's activity plan and related budget in line with unit strategy and area objectives.
  • Monitor the Communications budget, track actual versus forecast spending, identify deviations and take corrective measures.
  • Ensure compliance with GMP and HSE guidelines, internal and external requirements, and promote implementation and maintenance of company policies, systems and procedures within the team.
  • Carry out assigned tasks safely and in accordance with instructions and environmental, health and safety rules, procedures, regulations and codes of practice.

Desired Qualifications

  • A technical background 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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