Pharmaceutical Testing Jobs in Kentucky (NOW HIRING)

The Analytical Data Review Scientist is responsible for analyzing, tracking, and reporting laboratory and business data to support Eagle Analytical’s operations, quality, and compliance objectives. This role combines data analytics, programming, and business intelligence with hands‑on laboratory testing support, ensuring timely and accurate sample testing, data management, and documentation. The position requires technical expertise in data analytics, relational databases, and data visualization, as well as a strong understanding of laboratory processes, SOP compliance, and quality standards.

• Review analytical data, chromatographic reports, calculations, and laboratory worksheets for completeness, accuracy, and compliance with cGMP, cGLP, ISO 17025, USP, A2LA, and internal SOPs.
• Electronically sign off on data as both author and reviewer, following established procedures to ensure data integrity and regulatory compliance.
• Perform technical review and approval of Out-of-Specification (OOS) and Out-of-Trend (OOT) investigations, ensuring results meet regulatory and quality standards prior to release.
• Maintain accurate and current documentation of laboratory activities, SOPs, and forms.
• Write, revise, and review SOPs and related forms in a timely manner as required.
• Support laboratory compliance audits, internal quality audits, and safety audits.
• Participate in investigations of deviations, errors, and discrepancies, and assist with CAPA plans and risk assessments.
• Communicate with laboratory staff to proactively address documentation quality and resolve deficiencies.
• Perform routine and non-routine chemical analyses using HPLC, UPLC, GC, and spectrophotometry, as needed, under limited supervision.
• Process raw data using laboratory information management systems (e.g., EagleTrax, Empower) and ensure proper documentation and traceability.
• Perform routine testing on samples in a timely manner, tracking and meeting assigned deadlines.
• Notify supervisors promptly of unexpected test results and provide initial problem-solving with minimal supervision.
• Perform maintenance, calibration, and troubleshooting of assigned laboratory equipment and systems; report calibration failures or repair needs promptly.
• Maintain familiarity with all applicable laboratory equipment, systems, and SOPs.
• Assist across workstations as needed, providing backup support for all laboratory functions.
• Maintain clean, orderly, and safe laboratory work areas while observing personal safety protocols.
• Process and analyze data to generate reports to support laboratory operations, quality review activities, and timely release of results to clients and internal stakeholders.
• Provide consultative support to customers regarding technical questions related to testing, methods, or analytical results.
• Participate in team discussions and contribute to achieving laboratory goals.
• Stay current with emerging technology, instruments, and regulatory changes, with emphasis on HPLC and pharmaceutical analytical chemistry applications.
• Assist in training new hires in entry-level or laboratory support positions.
• Perform other duties and special projects assigned to support laboratory and quality operations.

• Bachelor’s or Master’s degree in Chemistry, Analytical Chemistry, Biochemistry, or a related science field.
• Minimum 2 years’ experience in a regulated pharmaceutical analytical laboratory, or equivalent combination of education and experience.
• Proficiency with analytical instruments (HPLC, UPLC, GC, UV/Vis spectrophotometer), including operation, troubleshooting, and maintenance.
• Experience with LIMS (e.g., Empower, EagleTrax) and electronic data review.
• Strong knowledge of cGMP, cGLP, ISO 17025, USP, A2LA, and data integrity principles.
• Experience with laboratory documentation, technical review of analytical data, and OOS/OOT investigations.
• Excellent attention to detail, organizational, and communication skills; ability to work independently and collaboratively.
• Proficiency in Microsoft Office.
• Experience with method development, validation, and transfer; familiarity with regulatory submissions and quality systems.
• Exposure to multiple laboratory workstations, cross‑functional operations, and providing technical consultation is a plus.
• Knowledge of emerging analytical technologies and pharmaceutical testing applications.

Serving customers since 2004, Eagle offers the highest quality in preparation testing for sterility, bacterial endotoxins, microbial detection, beyond‑use dating (BUD) determination and active ingredient potency. State‑of‑the‑art equipment, combined with the experience and knowledge of our team, makes Eagle the best choice for all testing needs. The Eagle team is committed not only to performing the best quality control testing, but also working relentlessly with our customers on solutions if tests receive unexpected results. Learn more at www.eagleanalytical.com.