Entry-Level Scientist - QC & Analytical Testing

Fresenius Kabi USA; Melrose Park (IL); On-site; USD 39,000 - 41,000; Full time

Benefits offered by this job

401(k) with company contributions

Health benefits

Dental & Vision coverage

Paid vacation & holidays

Wellness program

Job summary

Fresenius Kabi USA in Melrose Park, IL is seeking an entry-level Associate Scientist to perform routine chemical testing in support of raw materials, in-process, stability, and finished products, with emphasis on data accuracy and clear written/oral communication.

Responsibilities include executing FTIR, TLC, PM, UV-Vis analyses, documenting results per cGMP/GLP, updating SOPs in Documentum, and maintaining meticulous records while prioritizing tasks in a fast-paced quality environment.

Qualifications

• Bachelor's degree in a physical science; preferred in chemistry or biology.
• 0–2 years in pharmaceutical environment; familiarity with analytical methods a plus.
• Proficient with Microsoft Office (Word/Excel/PowerPoint).
• English language proficiency for policies, training materials, and workplace communications.

Responsibilities

• Articulate work issues clearly to management and peers.
• Perform routine chemical testing (FTIR, TLC, PM, UV-Vis) to meet objectives.
• Document testing in compliance with Good Documentation Practices.
• Update SOPs, MOAs, and Specifications in Documentum as delegated.
• Maintain accurate records and ensure compliance with cGMP/GLP requirements.
• Prioritize work based on departmental priorities and deadlines.

Skills

Communication skills

Time management

Education

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

Tools

HPLC

GC

AA

UV-Vis

TLC

FTIR

Documentum

Job description

Fresenius Kabi USA in Melrose Park, IL is seeking an entry-level Associate Scientist to perform routine chemical testing in support of raw materials, in-process, stability, and finished products, with emphasis on data accuracy and clear written/oral communication.

Responsibilities include executing FTIR, TLC, PM, UV-Vis analyses, documenting results per cGMP/GLP, updating SOPs in Documentum, and maintaining meticulous records while prioritizing tasks in a fast-paced quality environment.