Analytical Chemist II – QC & Instrumentation

Aurobindo Pharma USA, Inc.; Durham (NC); On-site; USD 65,000 - 75,000; Full time

Benefits offered by this job

Medical plans

Rx benefits

Dental plan

Vision plan

Life insurance

Disability insurance

401(k) with match

Employee Assistance Program (EAP)

Paid time off

Job summary

Aurolife, part of Aurobindo Pharma USA, Inc., in Durham, NC, is seeking an Analytical Laboratory Technician to perform sampling, testing, and data review of raw materials, in-process materials, and finished products in a cGMP environment.

You will operate and maintain instruments (HPLC, GC, UV, FTIR), ensure GLP compliance, participate in investigations, CAPA, and prepare SOPs and reports, while meeting timelines and upholding ALCOA+ data integrity.

Qualifications

• 3–5 years of pharma experience with 2–4 years in analytical testing.
• Experience in generic pharma preferred.
• Knowledge of GDP and data integrity (USP/ICH/FDA).
• Ability to learn quickly and make decisions.

Responsibilities

• Perform sampling and routine/advanced analyses of materials and products.
• Conduct testing with HPLC, GC, UV-Vis, FTIR and related instruments.
• Plan daily lab activities to meet timelines and resources.
• Maintain inventories of reagents and standards.
• Record data accurately in controlled records and systems.
• Support GDP, CAPA, investigations, and method validation.
• Prepare SOPs, protocols, and reports; ensure regulatory compliance.

Skills

Pharma experience

Analytical testing

GDP/USP/ICH/FDA

Decision making

Education

BS in science

Chemistry preferred

Tools

HPLC

GC

UV-Vis

FTIR

Particle Size Analyzer

Karl Fischer

Job description

Aurolife, part of Aurobindo Pharma USA, Inc., in Durham, NC, is seeking an Analytical Laboratory Technician to perform sampling, testing, and data review of raw materials, in-process materials, and finished products in a cGMP environment.

You will operate and maintain instruments (HPLC, GC, UV, FTIR), ensure GLP compliance, participate in investigations, CAPA, and prepare SOPs and reports, while meeting timelines and upholding ALCOA+ data integrity.