Scientist II or III - Device Verification Scientist - FSP

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 Scientist 2 or 3 - Device Verification Scientist position working as a full-time employee of Parexel on long-term assignment onsite at one of our clients located in West Point, PA. This position offers full benefits, sick time, 401K, paid holidays, and paid time off. This position does not offer sponsorship. Description: The Center for Packaging and Device Analytics (CPDA) provides physical analytical expertise in support of production and commercialization of packaging and combination device products. We are seeking a laboratory scientist to support characterization and testing of: (1) medical device combination product functionality and (2) primary packaging components (e.g. bottles, blisters) Work will involve hands-on laboratory experimentation with standard primary packaging assessments (e.g. Moisture ingress, UV transmission), mechanical testing methods (uniaxial tension, torsional testing), and/or other general materials characterization Individuals should have: (1) prior hands-on experience and proficiency with laboratory experimentation either in an academic or industry setting, (2) interest in hands-on physical applied science, (3) effective written communication skill for accurate, complete and clear laboratory notebooks and technical reports Qualifications: B.S. or M.S. Degree in Automated Sciences, Engineering, Chemistry, Biology or equivalent Scientist 2 - B.S. with 1-2 years of relevant experience or M.S. with >1 year of relevant experience Scientist 3 - B.S. with 3-5 years of relevant experience or M.S. with 1-2 years of relevant experience Required Skills and Experience: Prior hands-on scientific work in academic or industrial laboratory setting, backed by work reference(s) or publication(s) Flexible and adaptable team player who is technically curious, detail focused and seeks/takes feedback, but strives to deliver results independently Strong written and verbal communication Desired Skills and Experience: Experience in developing and executing mechanical test methods Experience with packaging characterization or device design verification testing Experience executing pharmaceutical test method validation Experience working in a GMP laboratory environment Software: MS office (Word, excel), ELN 100% onsite role, lab based. Work will primarily be 1st shift; however, project support may occasionally (5%) require flexibility to work some hours during 2nd shift About Parexel Parexel FSP includes the CMC Operations group. 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.