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Are you ready to make your mark in the healthcare industry using your ingenuity and technical expertise? At Parexel, there's no limit to what you can accomplish. We work with the top 50 global pharmaceutical companies, the top global biotech companies, and hundreds of small and emerging companies. We've supported the development of some of the most important treatments of our time, including nearly all of the 50 top selling drugs currently on the market. Join us and you'll make a profound difference in millions of lives. With a role in our Information Technology group, you'll work with cutting-edge technology on internal and client-facing projects. Collaborating with people from all over the world and touching everything from enterprise systems and clinical applications to infrastructure and networking, you'll keep our data safe and confidential. You'll have the chance to develop your skills and pursue advancement opportunities that include managerial and technical tracks. If you have stellar coding and design experience and a passion to learn more about healthcare, Parexel invites you to discover our rewarding opportunities in Enterprise Architecture, Software Development, Project Management and Business Analysis, and more. In a global clinical trial environment, business-focused applications, connectivity, and data security are critical to a trial's outcome. Find out how you can be an invaluable part of our success story.
Scientist III - Analytical Chemist - Chromatography Focus - FSP
Job ID R0000044603 PennsylvaniaWe 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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