Analytical Chemist II: GMP/GxP Data & Methods Expert

Actalent; North Chicago (IL); On-site; USD 44,000 - 48,000; Part time

Benefits offered by this job

Medical benefits

401(k) retirement

Life Insurance

Disability insurance

HSA

Transportation benefits

EAP

PTO

Job summary

Actalent in North Chicago, IL is seeking a Chemist II to plan and execute laboratory tasks across analytical techniques, generate precise data, and ensure full compliance with GxP, GMP, and GLP standards. You will interpret complex data and present findings to cross-functional audiences while maintaining safety and quality.

The role emphasizes protocol development for less defined assays, accurate documentation, and timely delivery of high-quality results in a fully onsite setting.

Qualifications

• Bachelor’s degree in a science field with lab experience is required.
• Experience with GMP/GLP and regulated environments is preferred.
• Strong data interpretation and documentation skills are essential.

Responsibilities

• Plan and execute lab tasks using standard procedures with sound judgment.
• Independently generate precise, reliable data within timelines.
• Document experiments in compliance with regulatory requirements.
• Develop protocols for complex tests and report findings to teams.
• Ensure safety and quality in all laboratory activities.
• Deliver high-quality, GxP-compliant data to support projects.
• Record data using word processing, spreadsheets, and instrument software.

Skills

Chemistry degree

Laboratory experience

GxP/GLP knowledge

Analytical instruments

Documentation skills

Regulated environment

Education

Bachelor's degree in Chemistry or related field

Master's degree in related field

Tools

Empower

OpenLab

Chromeleon

Job description

Actalent in North Chicago, IL is seeking a Chemist II to plan and execute laboratory tasks across analytical techniques, generate precise data, and ensure full compliance with GxP, GMP, and GLP standards. You will interpret complex data and present findings to cross-functional audiences while maintaining safety and quality.

The role emphasizes protocol development for less defined assays, accurate documentation, and timely delivery of high-quality results in a fully onsite setting.