Scientist, Data Review

Catalent • Morrisville, NC

13d • Onsite

About The Position

Catalent’s Morrisville facility, located in the heart of North Carolina’s Research Triangle Park, is a modern site dedicated to supporting advanced pharmaceutical development and manufacturing. The site offers comprehensive nasal development capabilities, including analytical support, device selection, spray characterization, and both clinical and commercial scale for unit‑dose, bi‑dose, and multidose nasal products. The Morrisville site also provides development services for dry powder (DPI) and liquid pulmonary products including formulation development and optimization, method services and analytical testing. Its strategic location within a leading life sciences hub fosters strong connections with industry partners and access to top talent, making it an exciting place to contribute to meaningful work that impacts global health.

Requirements

• Bachelor's or Master's degree in Chemistry, Pharmaceutical Sciences, or a related field of study
• Minimum 5+ years of experience in a pharmaceutical Quality Control (QC) laboratory environment
• Strong experience in data review, raw material testing, and compendial methods (USP/EP/JP)
• Knowledge of chromatographic and analytical techniques including High-Performance Liquid Chromatography (HPLC), Gas Chromatography (GC), and Fourier Transform Infrared Spectroscopy (FTIR)
• Strong understanding of current Good Manufacturing Practices (cGMP), data integrity, and regulatory expectations
• Proficiency in reviewing data from HPLC, GC, FTIR, Ultraviolet (UV), and wet chemistry techniques
• Must be able to wear safety glasses and a respirator when required
• Must have 20/20 vision (with or without corrective lenses)

Nice To Haves

• Familiarity with laboratory systems such as Empower, Laboratory Information Management System (LIMS), and TrackWise

Responsibilities

• Perform independent Level 2 review of analytical data for raw materials, packaging components, in-process, finished product, and stability samples
• Review and verify analytical test results generated using techniques such as High-Performance Liquid Chromatography (HPLC), Gas Chromatography (GC), Fourier Transform Infrared Spectroscopy (FTIR), Ultraviolet (UV), and wet chemistry in accordance with USP, EP, JP, and in-house methods
• Conduct audit trail reviews to ensure all data changes are traceable, justified, and compliant with data integrity (ALCOA+) requirements
• Review raw data, calculations, and documentation for accuracy, completeness, and data integrity compliance
• Verify system suitability, instrument performance, and method compliance during data review
• Support investigations including Out of Specification (OOS), Out of Trend (OOT), and deviations, and implement corrective and preventive actions (CAPA)
• All other duties as assigned

Benefits

• Medical, dental, and vision benefits effective day one of employment
• Tuition Reimbursement
• Defined career path and annual performance review and feedback process
• Potential for career growth on an expanding team within an organization dedicated to preserving and bettering lives
• Competitive paid time off plus 8 paid holidays
• Community engagement and green initiatives

What This Job Offers

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