Scientist 2 - Packaging and Device Analytics Distribution Testing Specialist - 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 - Packaging and Device Analytics Distribution Testing Specialist 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. 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. A laboratory scientist for the CPDA distribution laboratory will support distribution characterization and testing (e.g. ISTA, ASTM) of packaging configurations for standard primary packaging components (e.g. vials, bottles, blisters) and medical device-combination products (e.g. syringes). Work will involve hands-on experimentation and testing with both standard (e.g. ISTA, vibration, drop and shock testing) and fit-for-purpose characterization methods. Individuals should have prior hands-on laboratory (either in an academic or industry setting) and be capable/interested in hands-on physical science experimental work, and able to effectively document results in laboratory notebooks and technical reports. In addition to primary focus (supporting CPDA distribution lab), the scientist would potentially provide support for other CPDA project work (e.g. primary packaging characterization/assessments), as needed. 100% onsite role, lab-based. Work will be 1st shift. Qualifications: BS or MS Degree in Automated Sciences, Engineering, Chemistry, Biology or equivalent Scientist 2 - BS with 1-2 years of industry experience; or MS with no experience Required Skills and Experience: Prior hands-on lab experience in academic or industrial laboratory setting Personality: Flexible, adaptable, collaborative, team player, attention to detail and technically curious Strong written and verbal communication and attention to detail skills Proven ability to work independently Must be physically capable to lifting up to 35 pounds Software: MS office (Word, excel), ELN Desired Skills and Experience: Experience working in a laboratory/role directly supporting packaging distribution testing Experience with packaging testing and characterization Familiarity with standard package distribution testing methods (e.g. ISTA, ASTM) 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.