GMP Quality Control Analyst - Lab Compliance & Testing

Glenmarkpharma; Monroe (NC); On-site; USD 55,000 - 75,000; Full time

Job summary

Glenmark Pharmaceuticals Inc., USA is seeking a motivated QC Lab professional for the Monroe manufacturing facility. You will perform QC analyses in a cGMP environment, ensure data integrity, and support stability studies and instrument IOQ/calibration.

Reporting to the QC Manager, you will train staff, handle SOP updates, and participate in audits, tech transfers, and continuous improvement initiatives for finished products.

Qualifications

• B.Sc. in Chemistry with Biochemistry is required.
• 1–3 years in pharmaceutical manufacturing with QC exposure.
• Experience with HPLC, UV-Vis, FTIR and data integrity.

Responsibilities

• Perform QC analyses in a cGMP-compliant lab per USFDA.
• Maintain data integrity and support stability/IOQ activities.
• Train QC staff and ensure readiness for audits.
• Coordinate calibrations and maintenance of instruments.
• Prepare SOPs and support tech transfer and validation.

Skills

cGMP knowledge

Regulatory guidelines

Quality Assurance

SOP development

Education

B.Sc. in Chemistry with Biochemistry

Tools

HPLC

UV-Vis

FTIR

Lab instrumentation

Job description

Glenmark Pharmaceuticals Inc., USA is seeking a motivated QC Lab professional for the Monroe manufacturing facility. You will perform QC analyses in a cGMP environment, ensure data integrity, and support stability studies and instrument IOQ/calibration.

Reporting to the QC Manager, you will train staff, handle SOP updates, and participate in audits, tech transfers, and continuous improvement initiatives for finished products.