Senior Bioprocess Scientist (Innovation & Technology Development)

.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 I&TD Team has a vacancy in its team for the following position: Senior Bioprocess Scientist We are a pharmaceutical company with a clear purpose: to improve lives through innovative and sustainable manufacturing of medicines with Innovation is at the heart of the organization. Reporting to the I&TD laboratory Head, the Senior Bioprocess Scientist, will play a central role by (1) collaborating with a multidisciplinary team to design new processes for the manufacturing of APIs; (2) coordinate and leadrelevant works performed by our partners and CROs. The main activities and responsibilities Design new processes for the production of Centrient's new pipeline APIs. Oversee laboratory development work done by a multidisciplinary team of scientist and technicians. Project planning and management to achieve deadlines. Evaluate processes quality and safety for scale up readiness. Technology transfer to manufacturing site collaborating with Tech Ops team for a successful process implementation. Collaborate with cross-functional teams to integrate fermentation and enzymatic processes into overall drug development pipelines. Leading collaborations with partners and CROs with deep understanding of technologies applied. Compliance with GMP and Safety regulations in all activities. Monitors internal and external developments in the field for applicability, including benchmarking of the technology against competitors by performing literature and IP searches