QC Chemist II

Overview: Performs routine chemical analysis work involving pharmaceutical raw materials, process intermediates, and finished products in accordance with cGMPs, and SOPs under moderate supervision.Responsibilities:
Analyzes pharmaceutical raw materials, process intermediates and finished products, including stability samples, following approved test methods and procedures. Documents test results in accordance with standard operating procedures.
Special Projects and Training Others.
Training.
Performs routine chemical analysis work with moderate supervision.
Conducts chemical and physical analysis of raw materials, intermediate, finished products, and stability.
Calculates and Interprets test results and prepares test reports.
Notifies Supervisor of Out-of-Specification(OOS)/Out-of-Trend(OOT) samples.
Assists in OOS investigations to establish integrity of data.
Assists in training of new chemists, technicians, and assistants.
Operate, maintains, calibrates, and qualifies equipment in assigned area.
Performs related work assignments.
Capable of performing Special Projects under close supervision.
Basic Troubleshooting.
Reviews documentation.
Follows safety rules.
Proficient in computer usage.Job Requirements
Qualifications:
Four-year degree in a Science discipline with 2-5 years of relevant work experience, or equivalent.
Master’s Degree in a Science discipline with 1-3 year of relevant work experience, or equivalent.Knowledge of the principles and techniques of quantitative and qualitative chemical laboratory tests.
Skill in the operation of laboratory equipment (i.e. HPLC, GC, KF, pH meters, analytical balances, dissolutions etc).
Ability to conduct physical and chemical analyses and tests, to interpret test results, and to prepare concise reports.