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 III - Analytical Chemist- Chromatography Focus position working as a full-time employee of Parexel FSP 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 role will join a collaborative team of analytical chemists supporting non-clinical drug development across multiple therapeutic areas and modalities. The individual will contribute to sample management, GLP analytical testing, data interpretation, documentation, and compliance activities that enable the progression of development programs.
Qualifications
A Bachelor’s degree in chemistry or a closely related field with at least 3 to 5 years of relevant experience or a Master’s degree in chemistry or a closely related field with at least 1 to 2 years of relevant experience.
Responsibilities
Manage non-clinical study samples, including receipt, tracking, organization, and documentation.
Support execution of Good Laboratory Practice (GLP) activities, including dose formulation analysis using HPLC and related analytical techniques.
Document experimental procedures, execution, results, and conclusions in a detailed, organized, and compliant manner consistent with ALCOA principles.
Troubleshoot and investigate challenges associated with GLP testing through proactive collaboration with cross-functional non-clinical teams, Quality stakeholders, and other technical partners.
Perform data entry and data review, and author analytical reports, data summaries, and other study-supporting documentation.
Support compliance, audit, and inspection-readiness activities by ensuring work is accurate, traceable, and well documented.
Assist in maintaining the laboratory in a compliant, safe, and inspection-ready state.
Required Skills and Experience
Adaptability to changing assignments, schedules, and priorities while demonstrating strong problem-solving skills and effective verbal and written communication.
Good understanding of GLP compliance requirements and ALCOA documentation principles.
Strong computer, scientific, and organizational skills.
Excellent communication (oral and written) and attention to detail.
Excellent organization skills to multi-task and to manage multiple projects.
HPLC skills including routine sample analysis and instrument troubleshooting.
Ability to work independently and as part of a team.
Desired Skills and Experience
Experience with Empower software or a similar chromatography data system is a plus.
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!
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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.
Parexel is among the world’s largest clinical research organizations (CROs), providing the full range of Phase I to IV clinical development services to help life-saving treatments reach patients faster. Leveraging the breadth of our clinical, regulatory and therapeutic expertise, our team of more than 21,000 global professionals collaborates with biopharmaceutical leaders, emerging innovators and sites to design and deliver clinical trials with patients in mind, increasing access and participation to make clinical research a care option for anyone, anywhere. Our depth of industry knowledge and strong track record gained over the past 40 years is moving the industry forward and advancing clinical research in healthcare’s most complex areas, while our innovation ecosystem offers the best solutions to make every phase of the clinical trial process more efficient. With the people, insight and focus on operational excellence, we work every day to treat patients with dignity and continuously learn from their experiences, so every trial makes a difference. For more information, visit parexel.com.
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