Principal Scientist III - Synthetic Chemist

When our values align, there's no limit to what we can achieve. At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do. Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference. We are looking to fill a Principal Scientist III - Synthetic Chemist position working as a full-time employee of Parexel FSP on assignment onsite at one of our clients located in Rahway, NJ. This position offers full benefits, sick time, 401K, paid holidays, and paid time off. This position does not offer sponsorship. Description The Process Chemistry department of one of our clients in Rahway, NJ is seeking a highly motivated and experienced chemist who is looking for an opportunity to support the development, characterization, and commercialization of chemical manufacturing processes. Responsibilities Laboratory-based support of process development, characterization, and commercialization of small molecule manufacturing processes Laboratory work with a large variety of chemicals, using a diverse set of modern manual and automated laboratory equipment, and leveraging an array of analytical technology Non-lab-based work includes experimental planning, data analysis, and experiment documentation; review of peer work, and writing clear and concise development reports Qualifications Principal Scientist III - PhD degree in Chemistry with 3 years of professional experience in pharma/biopharma industry; or MS degree in Chemistry with 7 years of experience, or BS degree with 12 years of experience Required Skills and Experience Training must be in the field of organic synthesis, including synthetic methodology, catalysis, or total synthesis Demonstrably clear track record of both complex molecule synthesis and solving synthetic chemistry problems Experience in organic chemistry, organic synthesis, synthetic methodology, catalysis (including chemocatalysis, biocatalysis, and heterogeneous catalysis), total synthesis, physical organic chemistry, or flow chemistry Significant experience in chemical synthesis, compound purification, and analytical characterization, including HPLC, MS, and NMR techniques The ability to design and execute new synthetic routes to novel compounds Experience in process characterization, including Design of Experiments, fate and purge studies, and chemical marker preparation Strong written and oral communication skills and the ability to work effectively and with urgency in a collaborative and diverse team environment The ability to work independently with minimum supervision of daily tasks About Parexel FSP The CMC Operations group is part of Parexel FSP. We provide pharmaceutical and biopharmaceutical companies with qualified and talented technical professionals to support the development and delivery of new therapies. For results-driven and caring individuals who want to make a meaningful difference in the world, Parexel is trusted by life sciences companies to meet their long-term staffing needs for scientists and engineers and related professionals in discovery and development of novel therapies, keeping patients at the center of everything we do, and where an inclusive community helps you be your best, transforming any career into a life-changing achievement. Come join us! EEO Disclaimer Parexel is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to legally protected status, which in the US includes race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. Headquartered near Boston, Massachusetts and in Durham, North Carolina, Parexel has over 16,000 employees, with offices that support clients in over 100 countries around the world. We provide the most comprehensive drug development capabilities of any CRO worldwide. Our global regulatory expertise, Phase I-IV clinical research services, and advanced commercialization services all work together to move you through the development journey more smoothly and cost-effectively from beginning to end.