Senior Laboratory Instrumentation Specialist — Quality & Maintenance

Nephron Pharmaceuticals Corporation; Columbia (SC); Hybrid; USD 75,000 - 110,000; Full time

Job summary

Nephron Pharmaceuticals Corporation seeks a skilled professional to oversee laboratory instrumentation in the chemistry lab, ensuring reliable operation of HPLC, GC, and related tech. You will plan preventive maintenance, create SOPs, and manage supply needs while driving cost-efficiency and compliance.

This role requires strong project management, IT, and communication skills. Minimum Bachelor’s degree or 7 years in Quality Control Chemistry or R&D; experience with cGMP and FDA/USP standards is

Qualifications

• Experience with cGMP documentation systems and quality systems.
• Strong knowledge of FDA, USP, and industry requirements for analytical instrumentation qualification and maintenance.
• Direct experience with maintaining HPLC, GC, and other common laboratory instrumentation.
• Must possess strong IT skills and understanding of hardware and software troubleshooting of laboratory instrumentation.

Responsibilities

• Oversee all aspects of laboratory instrumentation in the chemistry laboratory.
• Plan, organize, and manage preventive maintenance of laboratory equipment.
• Create or modify SOPs, forms, and logbooks for the instrumentation program.
• Focus on cost savings and value delivery while maintaining high quality.

Skills

cGMP documentation

FDA/USP compliance

Project management

HPLC/GC maintenance

Instrumentation troubleshooting

IT skills

Attention to detail

Communication

Multitasking

Education

Bachelor’s degree or 7 years in QC Chemistry/R&D

Tools

Laboratory instrumentation maintenance

Job description

Nephron Pharmaceuticals Corporation seeks a skilled professional to oversee laboratory instrumentation in the chemistry lab, ensuring reliable operation of HPLC, GC, and related tech. You will plan preventive maintenance, create SOPs, and manage supply needs while driving cost-efficiency and compliance.

This role requires strong project management, IT, and communication skills. Minimum Bachelor’s degree or 7 years in Quality Control Chemistry or R&D; experience with cGMP and FDA/USP standards is