- Performs variety of tasks under general supervision
- Conforms to Company policies and procedures, Quality Systems, cGMP and FDA requirements.
- Represents the organization in a professional and positive manner.

- Requires Bachelors Degree in Chemistry, Biochemistry or related Science discipline with a minimum 4 (four) years experience in a Quality Control Analytical Laboratory within the pharmaceutical industry. Masters degree may be replaced with direct experience
- Thorough knowledge and hands-on experience of HPLC, GC, FTIR & UV/Visible spectrophotometer, Polarimeter, Karl-Fisher Titrator, Dissolution apparatus and wet chemistry techniques
- Excellent interpersonal and communication skills
- Ability to generate technical reports and demonstrate expertise in analytical software program
- Computer literacy with good working knowledge of statistical tools, MicroSoft Excel and Word