QC Chemist I

Quality Control Chemist position supporting analytical testing of raw materials, in-process samples, and finished products at a pharmaceutical services organization. Reports to Sr. Manager of QC & Analytical Development in Bedford, New Hampshire.

Responsibilities

• Perform routine analytical testing on raw materials, in-process, finished product, and stability samples
• Assist in deviation investigations, out-of-specification results, and process changes
• Author and review GMP documentation including test methods, protocols, and reports
• Log and track samples and chemicals; order laboratory supplies as needed
• Document and peer review laboratory work in compliance with cGMP/GDP requirements

Requirements

• 0-3 years analytical chemistry experience, preferably in quality control
• Bachelor of Science in Analytical Chemistry, Chemistry, or Pharmaceutical Sciences
• Knowledge of analytical instruments: HPLC, UPLC, FTIR, UV/VIS, pH meter, osmometer
• Strong attention to detail and problem-solving skills
• Excellent written and oral communication abilities
• Ability to multitask in dynamic environments with changing priorities