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1 semana atrás
Hovione is an independent family owned international group of companies with a strong presence in the pharmaceutical industry. Our innovative technological and productive capabilities have earned us a top spot in the world market as an integrated Contract Development and Manufacturing Company dedicated to helping Pharmaceutical Customers bring new and off-patent drugs to market.
About the Role- Responsibility over the development, scale-up, registration/validation of drug substance, particle engineering and drug development programs in compliance with legislation and regulatory standards of Quality, HSE and cGMP policies.
- Oversees the manufacturing process for clinical or commercial supplies of materials in cooperation with areas and supports safety/hazard analysis and other technical support areas as required.
- Promotes scientific excellence and innovation in the area and contributes with technical expertise to expand the Intellectual Property, product and technology portfolios.
- Leads the technical aspects of multiple complex projects.
- University, or equivalent, qualification in Chemistry, Chemical Engineering, Materials Sciences, Pharmaceutical Technology, Biological Engineering or Biology or Mechanical Engineering (specific for devices) or similar scientific field (mandatory), preferably with a PhD.
- Typically requires 5-8 years of relevant experience in Research & Development and/or Operations in the Pharmaceutical Industry. A Ph.D. degree in a relevant scientific field is typically considered equivalent to 4 years of relevant experience.
- Advanced knowledge of Chemical Engineering, Chemistry, Organic Chemistry and Unit Operations, or of Reaction Engineering, Heat Transfer, Scale-up, Process Safety and Industrial Operations, or of drug product unit operations, solids flow phenomena and process equipment, of drug product formulation and drug delivery; Mechanical Engineering and Fluid Dynamics with the ability to solve complex problems.
