| Celgene is a global biopharmaceutical company leading the way in medical innovation to help patients live longer, better lives. Our purpose as a company is to discover and develop therapies that will change the course of human health. We value our passion for patients, quest for innovation, spirit of independence and love of challenge. We are constantly looking for talented people to grow our business, advance our science and contribute to our unique culture. Celgene is seeking professionals at all levels of experience to join our Analytical Development (Small Molecules) department at our R&D facilities in New Jersey. Current opportunities include positions in: Solid State / Physical (Particle) Characterization Scientist, Methods Development (Chromatography) for DS and DP Scientists (Multiple positions at various levels: Entry Level through Senior Principal Scientist), Director - GMP Laboratories The professionals in these positions will contribute to (or lead) the analytical development for high priority drug candidates. You will identify and characterize key physical and/or chemical properties of pharmaceutical materials (e.g., active drug substances) and/or formulated drug products (e.g. tablets, injectable solutions). As an innovator, you will develop, validate and implement new analytical methods to guide product development and solve challenging technical problems related to purity, stability, packaging, and manufacturing. You will define strategies to address quality-related objectives, and will recommend the methods and specifications used to monitor pharmaceutical materials and/or the formulated product. You will then lead the transfer of these technologies to the manufacturing sites where they are used to verify that our commercial products comply with stringent quality requirements and regulatory standards. This professional will lead and/or participate on multi-disciplinary product development teams and will supervise the studies and professional development of one or more laboratory professionals. You will develop new scientific ideas, methods and technologies that contribute to the responsibilities described above. Other responsibilities include statistical data analysis, compliance with pharmaceutical good manufacturing practices and the completion of technical reports and external publications (as appropriate). |
