R&D Chemist II - Formulation & Method Development

Nephron Pharmaceuticals; West Columbia (SC); On-site; USD 120,000 - 150,000; Full time

Job summary

Nephron Pharmaceuticals is seeking an experienced R&D scientist to lead and execute research projects for established and new products. You will apply analytical method development and validation, perform stability studies, and support GMP compliance across regulatory submissions.

Responsibilities include drafting R&D and QC protocols, evaluating raw materials, and coordinating with QA to ensure on-time delivery of development summaries for clients and the FDA. Strong communication is essential.

Qualifications

• Master’s Degree in Chemistry; 8–10 years of experience in a cGMP environment.
• Experience in analytical method development and validation.
• Proven ability to manage multiple R&D projects with timelines.

Responsibilities

• Perform R&D projects including analytical method validation/transfer/verification, deformulation, and investigations.
• Plan, organize, and manage resources on projects to ensure quality and schedule adherence.
• Draft R&D and QC protocols and reports; develop methods for pharmaceutical ingredients.
• Support GMP data generation and ensure compliance with FDA and clients.
• Oversee development summaries documenting product development for clients and authorities.

Skills

LCMS analysis

HPLC/UPLC

GC

Mass Spectrometry

FT-IR

UV/Vis spectroscopy

Wet chemistry

Analytical testing

Project management

Scientific writing

Education

Master’s Degree in Chemistry

Tools

HPLC systems

Mass spectrometers

FT-IR spectrometers

Analytical instrumentation

Job description

Nephron Pharmaceuticals is seeking an experienced R&D scientist to lead and execute research projects for established and new products. You will apply analytical method development and validation, perform stability studies, and support GMP compliance across regulatory submissions.

Responsibilities include drafting R&D and QC protocols, evaluating raw materials, and coordinating with QA to ensure on-time delivery of development summaries for clients and the FDA. Strong communication is essential.