QC Chemist

, Pharma Manufacturing

Our client is a cGMP contract manufacturing company with expertise in research & development, manufacturing, packaging and testing of products. Working with many different industries, they offer expertise in manufacturing but also packaging in various dosage forms. They can produce your current products, improve on existing products or develop new products to help you meet your goals.

Location:Northeast Philadelphia

Responsibilities

• Analysis of raw materials, finished products and stability samples by HPLC/UV and other lab techniques
• Analytical Method Validation as per regulatory guidance (ICH, FDA, USP, BP, EP etc) for new formulations including but not limited to Tablets, Capsules, Gels, Pastes, Creams and Oral solutions/Suspensions
• Review of analytical data
• Perform method transfer activity with various customers
• Perform various analytical tests to ensure product meets all specifications
• Calibration of various analytical instruments (HPLC, Spectrophotometer, dissolution apparatus etc.)

Requirements

• Minimum 2 years' industrial experience in Quality Control laboratory functions, specifically using HPLC
• A Degree (BS or BA) in Biology, Chemistry, Biochemistry, or relevant related field. Or sufficient technical depth or professional experience will be considered in lieu of technical degree.