Analytical Development Scientist: Method Transfer Expert

ESTEVE; Morton Grove (IL); On-site; USD 85,000 - 120,000; Full time

Job summary

ESTEVE is seeking an Analytical Development Scientist to develop, optimize, validate, and transfer analytical methods for pharmaceutical products. You will work with QC, Manufacturing, Regulatory, and Validation to ensure methods are scientifically sound and compliant with regulatory requirements.

You will perform testing using HPLC, GC, dissolution, UV-Vis, FTIR, and KF, interpret data, and contribute to regulatory submissions while supporting continuous improvement in a cGMP environment.

Qualifications

• Bachelor's degree in Chemistry, Pharmaceutical Sciences, Analytical Chemistry, or related scientific discipline.
• 3–5 years of pharmaceutical analytical development or related lab experience in a cGMP-regulated environment.
• Strong knowledge of chromatographic and analytical techniques (HPLC, GC).
• Proficiency in data analysis, technical writing, and problem solving.
• Excellent verbal and written communication skills.

Responsibilities

• Develop, optimize, validate, and transfer analytical methods for APIs, finished products, intermediates, and raw materials.
• Perform analytical testing using HPLC, GC, dissolution, UV-Vis, FTIR, KF, and related instruments.
• Document data and results in compliance with GMP and data integrity requirements.
• Prepare and review methods, protocols, reports, specifications, and SOPs.

Skills

Problem solving

Technical writing

Data analysis

Verbal/written communication

Education

Bachelor's degree: Chemistry/Pharmaceutical Sciences/Analytical Chemistry

Tools

HPLC

GC

Dissolution

UV-Vis

FTIR

KF

Laboratory software

Microsoft Office

Job description

ESTEVE is seeking an Analytical Development Scientist to develop, optimize, validate, and transfer analytical methods for pharmaceutical products. You will work with QC, Manufacturing, Regulatory, and Validation to ensure methods are scientifically sound and compliant with regulatory requirements.

You will perform testing using HPLC, GC, dissolution, UV-Vis, FTIR, and KF, interpret data, and contribute to regulatory submissions while supporting continuous improvement in a cGMP environment.