Research and Development Scientist. Basel-Stadt. Suiza
Oferta en Suiza (Basel-Stadt) de Profesionales científicos e intelectuales
Clasificación del trabajo:Profesionales científicos e intelectuales. Akademische Berufe.
Descripción de la oferta de trabajo:
Description Amaris is an independent, international Technologies and Management Consulting Group. Created in 2007, Amaris is already established in over 50 countries and supports 500 clients worldwide throughout their projects’ lifecycle. Our expertise covers 5 areas of innovation: Business and Management, IT/IS, Telecom, Engineering and High Technologies, Biotech and Pharma. With 65 offices across the World, the Group offers proximity support to its clients in all their locations and many opportunities of international careers for employees. In 2017, Amaris aim to reach a turnover of 180 million euros, 3500 employees and the ability to recruit one new employee every 5 hours. We expect to triple our workforce within the next years and reach an international leader position in independent consulting. Your Role Your role You will join Amaris as a consultant and be part of a team coordinated by your manager. Together you will design drugs and management solutions for our clients in the Pharmaceutical Industry. You will be present on client’s plant to work on mid and long term projects in Research and Development of new drugs. You will be working in multidisciplinary network organization, an international teams and representing Pharmaceutical Development in external collaborations, which results in a wide range of scientific and strategic tasks. Your role as a Research and Development Scientist will be to support and contribute to the implementation and optimization of projects of the clients. You will be responsible for a variation of aspects within the projects of our clients such as: - development of oral dosage forms and the transfer to production. - ensure that high quality products are developed applying state of the art technologies, risk analysis and QbD methodologies. - achieve robust formulations and processes through optimization, scale-up and validation work and provision of the required documentation to allow worldwide registration. (oral, tablets, liquid, sterile…) - Project management on technical and clinical manufacturing of oral solid. - dosage forms: organize activities, rooms, material, write MBR, participate to CMC meetings, collaborate with QA and QC. - The development of new processing technologies and supervision of scientific projects are further options within this position. Profile You have received a scientific education (PhD): engineer, chemist, biologist, and pharmacist or similar. You know the legal requirements for pharmaceutical industry (cGMP) and have at least two year works experience in such pharmaceutical environment, of which maintenance, calibration and management planning experience in the last six months. You are proactive, have good communication skills, and are capable of working in a multidisciplinary team towards a common goal. You are proficient in English (spoken and written), German and French is a plus.
Servicio de empleo de origen:SECO, Servicios Públicos de Empleo, Suiza.