Scientist III - Analytical Chemist - Chromatography Focus - FSP

Parexel • United States-Pennsylvania-Remote, PA

1d • Onsite

About The Position

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.

Requirements

• 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.
• 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.

Nice To Haves

• Experience with Empower software or a similar chromatography data system is a plus.

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.

Benefits

• full benefits
• sick time
• 401K
• paid holidays
• paid time off

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level