Job Description

📍 Location: Pennington, NJ (100% Onsite)

🕒 Schedule: Contract | 40 hrs/week | Mon–Fri | 8 hrs/day

📅 Start Date: August 4, 2025 | End Date: January 4, 2026

Join a high-impact team supporting essential pharmaceutical manufacturing operations!

We’re seeking a detail-oriented and proactive QC Chemistry Analyst to support quality control processes at a cutting-edge biotech facility. In this role, you'll play a key part in ensuring timely test result reporting, maintaining sample integrity, and upholding regulatory compliance in a fast-paced, FDA-regulated environment.

What You’ll Do:

• Establish and maintain a QC sample management program to support critical manufacturing timelines
• Coordinate time-sensitive distribution of QC samples and oversee stability sample management
• Perform key operational tasks such as instrument qualification, SOP updates, CoA generation, and data record keeping
• Manage inventory for reference standards and QC samples, including on-test, retain, reserve, and stability samples
• Support documentation and compliance activities aligned with cGMP and global regulatory standards

What You Bring:

• Bachelor’s degree or higher in Chemistry, Biotechnology, or a related scientific field
• Minimum of 2 years’ experience in an FDA-regulated biotech or pharmaceutical company (5+ years preferred)
• Hands-on experience with analytical testing, sample management, and lab instrumentation
• Strong knowledge of USP/EP, cGMP, EU GMP, and equipment validation procedures
• Detail-oriented with excellent organizational, communication, and time-management skills
• A proactive, problem-solving mindset and a collaborative, team-first attitude

Job Tags

Similar Jobs