Quality Control Chemist

Ajulia Executive Search; Rock Hill (SC); On-site; USD 55,000 - 85,000; Full time

Benefits offered by this job

Full benefits package

Job summary

Ajulia Executive Search is seeking a Quality Control Chemist for a 2nd shift in the Rock Hill, SC area. The role requires hands-on experience with HPLC and GC in a pharmaceutical setting and a strong understanding of cGMPs.

Responsibilities include instrument operation, routine testing, documentation, and SOP development to ensure regulatory compliance. Competitive benefits accompany a full-time position.

Qualifications

• Bachelor's degree in Chemistry, Biochemistry, Biotechnology or related field.
• Pharmaceutical industry experience with analytical techniques such as HPLC and GC.
• Knowledge of cGMPs, quality concepts and Microsoft Office.
• Excellent written and verbal communication skills.

Responsibilities

• Follow cGMP and maintain accurate lab documentation.
• Operate analytical instruments (HPLC, GC, FTIR, UV/Vis) and troubleshoot as needed.
• Perform routine and in-process testing on finished products and raw materials.
• Develop and update SOPs for the laboratory and conduct lab audits.
• Ensure compliance with regulatory requirements.

Skills

HPLC

GC

FTIR

UV/Vis

Titrators

cGMP

Education

Chemistry degree

Biochemistry degree

Biotechnology degree

Tools

Microsoft Office

Job description

Gas Chromatography (GC) and/or Liquid Chromatography (LC).

Immediate Hire

2nd Shift

Are you looking to make a career change to a rapidly growing, stable, innovating company? This exciting opportunity as a Quality Control Chemist offers a competitive salary plus an excellent benefits package including medical insurance, dental insurance, vision insurance, paid PTO etc. Does this position match your future career goals? Then this Quality Control Chemist opportunity could be the right fit for you.

• QC experience in the Pharmaceutical industry.
• High Performance Liquid Chromatography (HPLC), Gas Chromatography (GC), Automated Titrators, FTIR and UV/Vis Spectrophotometer.

Compensation

Full benefits package

Responsibilities:

• Follow Current Good Manufacturing Practice (cGMP)
• Adapt, maintain and operate analytical instrumentation such as HPLC, GC, FTIR, TOC, UV, etc. and minor trouble shooting of equipment.
• Perform routine laboratory analysis, such as finished product testing, dissolution testing, stability testing, raw material testing, cleaning verification testing and manufacturing in-process testing.
• Documentation of log books, in-house calibration records, temperature and humidity records, etc.
• Perform analytical testing on finished products, In-process (Blend Uniformity), and Cleaning Validation samples.
• Developing, reviewing, and updating standard operating procedures for the laboratory.
• Conducting regular audits to ensure all lab processes are running correctly.
• Ensuring compliance with industry and regulatory.

Requirements:

• Bachelor's degree in Chemistry ,Biochemistry, Biotechnology or related field.
• Must have prior experience working in the Pharmaceutical industry, using analytical techniques including HPLC and GC.
• Must have knowledge of cGMPs, Quality Concepts, and Microsoft Office.
• Excellent written and verbal communication skills.