Analytical Chemist I — QC & R&D Lab Specialist

Nephron Pharmaceuticals Corporation; Columbia, Northern (SC, KY); Hybrid; USD 52,000 - 75,000; Full time

Job summary

Nephron Pharmaceuticals Corporation is seeking a Quality Control Analyst to support routine laboratory testing for raw materials, in-process materials, finished product, and stability samples. The role emphasizes adherence to approved analytical methods and GDP/cGMP standards.

The candidate should have a BS or MS in Chemistry or related field with 0–3 years of pharmaceutical experience, and hands-on experience with FT-IR, UV/Vis, HPLC, and GC.

Qualifications

• Requires BS or MS in Chemistry, Biochemistry, or related field with 0–3 years pharmaceutical experience preferred.
• Experience with FT-IR, UV/Vis spectroscopy, and wet chemistry techniques is required.
• Experience with HPLC and GC is preferred; knowledge of analytical methods and specifications is essential.

Responsibilities

• Conduct routine laboratory testing for raw materials, in-process materials, finished product, and stability samples.
• Perform data analysis and interpretation using approved specifications and methods.
• Peer review notebooks and verify raw data to support sample release and data integrity.
• Enter data into reporting systems and completion of release forms.
• Follow GDP and cGMP requirements and maintain compliance with SOPs.

Skills

Strong analytical skills

Problem-solving ability

Attention to detail

cGMP knowledge

USP standards knowledge

SOPs reading/writing

Effective communication

Continuous improvement mindset

Education

BS or MS in Chemistry/Biochemistry/related field

Tools

FT-IR

UV/Vis spectroscopy

HPLC

GC

Job description

Nephron Pharmaceuticals Corporation is seeking a Quality Control Analyst to support routine laboratory testing for raw materials, in-process materials, finished product, and stability samples. The role emphasizes adherence to approved analytical methods and GDP/cGMP standards.

The candidate should have a BS or MS in Chemistry or related field with 0–3 years of pharmaceutical experience, and hands-on experience with FT-IR, UV/Vis, HPLC, and GC.