Analytical Chemist II: QC & R&D Lab Specialist

Nephron Pharmaceuticals Corporation; West Columbia (SC); On-site; USD 55,000 - 85,000; Full time

Job summary

Nephron Pharmaceuticals Corporation is seeking a Chemist to support quality control testing and R&D activities. The role involves conducting laboratory tests on raw materials, in-process materials, finished products, and stability samples using validated analytical methods.

Ideal candidates hold a BS or MS in Chemistry/ Biochemistry with 2–5 years of pharmaceutical QC/R&D experience and strong analytical skills aligned with cGMP standards. Safety and compliance are essential in daily operations.

Qualifications

• BS or MS in Chemistry, Biochemistry, or related field.
• 2-5 years of pharmaceutical experience preferred.
• Experience with FT-IR, UV/Vis spectroscopy, and wet chemistry techniques required.

Responsibilities

• Conduct routine and complex laboratory testing for raw materials, in-process materials, finished product, and stability samples.
• Perform testing using validated analytical methods and ensure compliance with GDP and cGMP requirements.
• Analyze and interpret data using specifications and test methods.
• Peer review notebooks and verify raw data to support sample release.
• Enter data into reporting systems and release forms accurately.
• Mentor and train chemists to support laboratory operations.
• Troubleshoot equipment and analyses as needed.
• Assist in investigation documentation.

Skills

Analytical thinking

Attention to detail

Communication skills

Problem-solving

Continuous improvement

Team collaboration

Education

BS or MS in Chemistry/Biochemistry or related field

Tools

FT-IR

UV/Vis spectroscopy

HPLC

GC

ICP testing

Job description

Nephron Pharmaceuticals Corporation is seeking a Chemist to support quality control testing and R&D activities. The role involves conducting laboratory tests on raw materials, in-process materials, finished products, and stability samples using validated analytical methods.

Ideal candidates hold a BS or MS in Chemistry/ Biochemistry with 2–5 years of pharmaceutical QC/R&D experience and strong analytical skills aligned with cGMP standards. Safety and compliance are essential in daily operations.