Quality Control Scientist I - HPLC & GMP Testing

Fresenius SE & Co. KGaA; Melrose Park (IL); On-site; USD 41,328 - 44,083; Full time

Job summary

Fresenius Kabi in Melrose Park, IL, seeks a Scientist I in Quality Control to apply analytical chemistry and chromatography expertise to routine testing and troubleshooting within a regulated environment.

The role includes directing and guiding associate scientists, ensuring documentation per Good Documentation Practices, and maintaining compliance with cGMP and FDA requirements while coordinating with supervision.

Qualifications

• B.S. in Chemistry, Biology or related physical science.
• 1-4 years of pharmaceutical industry experience.
• Hands-on experience with chromatographic methods and Empower data systems.
• Proficiency in Microsoft Office (Word, Excel).

Responsibilities

• Be able to articulate work related issues clearly and effectively to management and peers
• Performs accurate routine testing utilizing instrumental methods of analysis (HPLC, TLC, FTIR, pH, UV-Vis) with emphasis on chromatography to meet departmental objectives.
• Updates and routes SOPs, MOAs, Specifications through Documentum as delegated by supervisor.
• Performs troubleshooting of instrumentation by applying problem solving skills.
• Provides guidance to Associate Scientist personnel when necessary.
• Documents testing in compliance with Good Documentation Practices
• Manages work and time based on departmental priorities using own judgement and objective reasoning.
• Performs peer review of data to ensure compliance and accuracy.

Skills

Chromatography knowledge

Microsoft Office

Communication skills

Documentation practices

Education

B.S. in Chemistry, Biology or related physical science

Tools

Empower

Job description

Fresenius Kabi in Melrose Park, IL, seeks a Scientist I in Quality Control to apply analytical chemistry and chromatography expertise to routine testing and troubleshooting within a regulated environment.

The role includes directing and guiding associate scientists, ensuring documentation per Good Documentation Practices, and maintaining compliance with cGMP and FDA requirements while coordinating with supervision.