Pharma QC Chemist: Analytical Testing & Mentorship

Acrotech Biopharma inc.; South Brunswick (NJ); On-site; USD 85,000 - 90,000; Full time

Benefits offered by this job

Medical & Rx

Dental

Vision

Life Insurance

Disability

401(k)

EAP

PTO

Job summary

Aurolife in South Brunswick, NJ, is seeking a Chemist-C to perform QC testing to assess the strength, identity and purity of materials. You will work at the bench, document results, and mentor junior analysts to ensure accuracy and compliance.

The role requires planning testing, maintaining reagents, reviewing procedures, and upholding cGMP standards. A BS in a scientific field with 4–6 years pharma experience is preferred.

Qualifications

• Knowledge in Good Documentation practices and USP/ICH/FDA requirements.
• Ability to learn quickly and exercise sound decision making.
• Attention to detail and thorough documentation.
• Proficient with Empower and LIMS systems.
• 2-4 years experience handling Out Of Specification investigations.

Responsibilities

• Perform sampling, tests and assays on materials using USP/in-house methods.
• Plan and inventory reagents; ensure supplies for testing.
• Plan and execute testing to meet established timelines; assist where needed.
• Record data per procedures and maintain clear documentation.
• Prepare and review Test Procedures, SOPs, and Protocols.
• Calibrate and maintain laboratory instruments under supervision.
• Troubleshoot and investigate issues with supervision.
• Adhere to safety, cGMP, cGLP and regulatory requirements.
• Review analytical documents as required.
• Mentor and train new chemists; act as role model.

Skills

Good Documentation

USP/ICH/FDA knowledge

Decision making

Attention to detail

Empower & LIMS experience

Education

BS in Chemistry or scientific field

4-6 years pharma experience

3+ years Analytical testing

Tools

Empower

LIMS

Job description

Aurolife in South Brunswick, NJ, is seeking a Chemist-C to perform QC testing to assess the strength, identity and purity of materials. You will work at the bench, document results, and mentor junior analysts to ensure accuracy and compliance.

The role requires planning testing, maintaining reagents, reviewing procedures, and upholding cGMP standards. A BS in a scientific field with 4–6 years pharma experience is preferred.