Pharma QC Chemist – Analytical Testing & GMP

Aurobindo Pharma USA, Inc.; Durham (NC); On-site; USD 50,000 - 60,000; Full time

Benefits offered by this job

Medical benefits

Dental benefits

Vision plan

Life Insurance

Disability Insurance

401(k)

Job summary

Aurolife in Durham, NC seeks a Chemist A to perform QC testing, assessing strength, identity and purity of samples. You will work with bench-level procedures, following established methods and regulatory guidelines.

The role requires 2–3 years in pharma and 1–2 years in analytical testing, with knowledge of GMP practices. Travel and working in a controlled environment are part of the job, with comprehensive benefits available.

Qualifications

• BS in Chemistry or related field required.
• 1–2 years in analytical testing preferred.
• 2–3 years in pharmaceuticals experience desirable.
• Knowledge of GMP practices and regulatory guidelines.

Responsibilities

• Perform sampling, physical, chemical tests and assays on raw materials, in-process, finished products and stability samples per USP or in-house methods.
• Plan and maintain inventory of test reagents and solutions.
• Plan and execute testing to meet established timelines; perform complex testing with supervisory direction.
• Record data and results according to procedures; document work clearly.
• Prepare/review Test Procedures, SOPs, and Protocols as assigned.
• Perform maintenance and calibration of laboratory instruments with supervision.
• Conduct troubleshooting under supervision.
• Comply with regulatory and in-house requirements (cGMP, cGLP, safety).
• Review analytical documents as required.

Skills

Good Documentation Practices

USP/ICH/FDA guidelines

Analytical testing experience

Decision making

Team collaboration

Education

BS in Chemistry or related field

Tools

HPLC

GC

UV-Vis

IR

Particle size analyzer

KF titrator

Bulk density

Job description

Aurolife in Durham, NC seeks a Chemist A to perform QC testing, assessing strength, identity and purity of samples. You will work with bench-level procedures, following established methods and regulatory guidelines.

The role requires 2–3 years in pharma and 1–2 years in analytical testing, with knowledge of GMP practices. Travel and working in a controlled environment are part of the job, with comprehensive benefits available.