R&D Data Review Scientist I

Actalent; Cincinnati (OH); On-site; USD 39,000 - 55,000; Full time

Benefits offered by this job

Medical, dental & vision

401(k) Retirement Plan

Pre-tax and Roth post-tax

Life Insurance

Short and long-term disability

Health Spending Account (HSA)

Transportation benefits

Employee Assistance Program

PTO / Vacation / Sick Leave

Job summary

Actalent is hiring an Associate Scientist I - R&D (Data Review Scientist I) in Cincinnati, OH. This role focuses on reviewing analytical data and documentation from QC laboratories to ensure accuracy, completeness, and regulatory compliance, supporting product release and quality activities.

The position operates in a GMP-regulated environment with a second-shift schedule (2:00 p.m. start) and is contract to hire.

Qualifications

• Bachelor's degree in a scientific field (Chemistry, Biology, Biochemistry) is required.
• 2+ years of relevant experience in a regulated lab environment is preferred.
• Experience with data review or analytical lab testing is preferred.
• Working knowledge of analytical techniques such as HPLC, GC, spectroscopy, dissolution testing, and wet chemistry.
• Knowledge of GMP, Good Documentation Practices, pharmaceutical quality standards, and data integrity principles.

Responsibilities

• Review analytical data, lab records, and supporting documentation for accuracy and compliance.
• Review data from HPLC, GC, spectroscopy, dissolution testing, and wet chemistry methods.
• Verify calculations, test results, specifications, instrument outputs, chromatograms, and associated documentation.

Skills

HPLC

GC

Spectroscopy

Dissolution testing

GMP

Data integrity

Communication skills

Problem solving

Education

Bachelor's degree in Chemistry/Biology/Biochemistry

Tools

LIMS

Electronic data systems

Microsoft Office

Job description

Actalent is hiring an Associate Scientist I - R&D (Data Review Scientist I) in Cincinnati, OH. This role focuses on reviewing analytical data and documentation from QC laboratories to ensure accuracy, completeness, and regulatory compliance, supporting product release and quality activities.

The position operates in a GMP-regulated environment with a second-shift schedule (2:00 p.m. start) and is contract to hire.