Quality Control Chemist

ClearBridge Executive Search; Rock Hill (SC); On-site; USD 60,000 - 76,000; Full time

Benefits offered by this job

Medical, dental, and vision

Paid PTO

Job summary

ClearBridge Executive Search is hiring a Quality Control Chemist for the 2nd shift in South Carolina. The role focuses on analytical testing, instrument maintenance, and cGMP compliance in a pharmaceutical setting.

The ideal candidate has a Chemistry degree and experience with HPLC and GC, with strong documentation and communication skills. Excellent benefits, PTO, and growth opportunities are offered.

Qualifications

• Bachelor's degree in Chemistry (or Biochemistry/ Biotechnology related field).
• Pharmaceutical industry QC experience is preferred, with proficiency in HPLC and GC.
• Knowledge of cGMPs and quality concepts; proficient with Microsoft Office.

Responsibilities

• Operate and maintain analytical instrumentation including HPLC, GC, FTIR, TOC, UV/Vis, with minor troubleshooting.
• Perform routine laboratory analyses: finished product testing, dissolution, stability, raw material, cleaning verification, and in-process testing.
• Document logbooks, calibration records, and environmental monitoring (temperature/humidity).
• Conduct analytical testing on finished products, blend uniformity, and cleaning validation samples.
• Develop, review, and update SOPs for laboratory operations.
• Perform internal audits to ensure compliance with cGMP and regulatory standards.
• Collaborate with cross-functional teams to maintain quality and compliance.

Skills

Communication skills

Attention to detail

Organizational skills

Microsoft Office

Education

Bachelor's degree in Chemistry

Tools

HPLC

GC

FTIR

TOC

UV/Vis

Job description

Quality Control Chemist – Immediate Hire (2nd Shift)

Overview

Join a rapidly growing, stable, and innovative pharmaceutical company as a Quality Control Chemist. This role offers a competitive salary and a full benefits package, including medical, dental, vision, and paid PTO. If you are seeking a career move into a dynamic environment with growth opportunities, this position could be the right fit.

Key Responsibilities

• Operate and maintain analytical instrumentation including HPLC, GC, FTIR, TOC, UV/Vis, with minor troubleshooting.
• Perform routine laboratory analyses: finished product testing, dissolution, stability, raw material, cleaning verification, and in‑process testing.
• Document logbooks, calibration records, and environmental monitoring (temperature/humidity).
• Conduct analytical testing on finished products, blend uniformity, and cleaning validation samples.
• Develop, review, and update SOPs for laboratory operations.
• Perform internal audits to ensure compliance with cGMP and regulatory standards.
• Collaborate with cross‑functional teams to maintain quality and compliance.

Requirements

• Bachelor’s degree in Chemistry (Biochemistry, Biotechnology, or related field acceptable).
• Prior pharmaceutical industry QC experience with strong proficiency in HPLC and GC.
• Knowledge of cGMPs, quality concepts, and Microsoft Office.
• Excellent written and verbal communication skills.
• Strong attention to detail and organizational skills.
• Full benefits package (medical, dental, vision, PTO)