Analytical Development Scientist

hace 6 días

Barcelona, España Centrient Pharmaceuticals Netherlands A tiempo completo

.Centrient Pharmaceuticals is the leading manufacturer of beta-lactam antibiotics, and a provider of next generation statins and anti-fungals. We produce and sell intermediates, active pharmaceutical ingredients and finished dosage forms.We stand proudly at the centre of modern healthcare, as a maker of essential and life-saving medicines.With our commitment to Quality, Reliability and Sustainability at the heart of everything we do, our over 2200 employees work continuously to meet our customers' needs. We work towards a sustainable future by actively participating in the fight against antimicrobial resistance.Founded 150 years ago as the 'Nederlandsche Gist- en Spiritusfabriek', our company was known as Gist Brocades. Headquartered in Rotterdam (Netherlands), we have production facilities and sales offices in China, India, the Netherlands, Spain, the United States and Mexico. Centrient Pharmaceuticals is wholly owned by Bain Capital Private Equity, a leading global private investment firm.The Innovation & Technology Development department has a vacancy in its team for the following position:Analytical Development Scientist (Innovation & Technology Development)The Innovation and Technology Development (I&TD) team is expanding capabilities and key competences, with analysis identified as a critical tool to deliver into our innovation journey. The Analytical Development Scientist carries out the development, validation and transfer of new analytical methods (sample preparation, chromatographic analysis, spectroscopic techniques, PSD analysis, etc.) and analytical techniques to support the development of API and its intermediates, scale up, process validation, tech transfer, pre-stability and stability studies. Supports the different projects from the analytical point of view.The main activities and responsibilitiesDevelopment, validation and transfer of analytical methods.Editing and revision of ICH stabilities and validations documentation.Investigation of analytical incidents and OOS reports.Participation in the industrialization of new processes.Participation in I&TD project teams.Collaboration in Master Plans for Validation / Homologation.Editing and reviewing the regulatory documentation necessary to support new registrations and variations.Project management within the industrial pharmaceutical development environment.The Ideal CandidateBachelor's and/or Master's degree in a relevant life science field such as Chemistry, Biochemistry, Pharmacy or similar.Minimum of 5 years of experience in method development and validation preferably in pharmaceutical industry.Fluent in English language (written and spoken).Knowledge of ICH and GMP.Experience in the development of projects in the R&D area.Adaptable, self-motivated and curious systems thinker.Decision making and results oriented.Strong communication skills

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