Senior Research Associate, Analytical Development

This position is within Synta's Drug Product Development group and requires the ability to conduct analytical support for drug product development activities.

Responsibilities:

Perform HPLC method development, optimization and qualification for testing drug substances, intermediates and drug products.

Test samples from stability studies or drug- excipient compatibility studies.

Preparing technical reports, summaries, protocols and quantitative analyses

Assisting Scientists and Sr. Scientists in performing research and development activities as a team

Presenting data in team and department meetings

Routine service and maintenance of analytical laboratory equipment and supplies

Qualifications:

This position requires a bachelor's degree with a minimum of 5-8 years or a master's degree and a minimum of 3-5 year's working experience in analytical development or quality control environment of a pharmaceutical company.

Experienced with analytical method development/validation for API and various dosage forms (solid oral, sterile liquid/solid), familiar with FDA, ICH and GMP guidelines.

Hands-on experience in using analytical balance, pH meter, Karl-Fischer titrator and HPLC. Experience on using DSC, TGA and Particle size analyzer is an advantage.

Working knowledge of impurity identification and quantification, pre-formulation or formulation is desirable.

Strong writing and oral communication skills and able to work well within the team and with other groups.

Experience working with CRO is a plus.

Willingness to learn and expand their knowledge and technical expertise in a motivated and fast paced environment.