Sr. Research Associate (dissolution stability) (v258)

  • Contract Duration: 12 months (Temp to Perm)
  • Research & Development
  • Boston, MA

Website Lenox Executive Search

Description

Lenox Executive Search has a client in Boston seeking a talented Research Associate to join their Analytical Development team. Our client is an industry leader in the pharmaceutical space and continues to grow year over year.

This role is a 1-year contractual role with the possibility of conversion to full time employment based on job performance.

Position Overview:

Seeking a talented employee to join our Analytical Development group in Boston, MA. Consistently and passionately challenging the boundaries of their knowledge, our Analytical Development team employs traditional and innovative analytical techniques and Quality-by-Design principles to develop and validate the analytical tools used to ensure the safety, efficacy and quality of client’s pharmaceutical products.

As a member of the Analytical Development team, this role will support the drug development programs at client through dissolution testing and dissolution method development. The ideal candidate will have proven experience in dissolution testing with the ability to excel in a fast paced environment.

Key Responsibilities:

– Develops, troubleshoots and conducts dissolution experiments in support of drug product process development

– Performs dissolution stability testing on drug products

– Maintains accurate records of experiments and results in an electronic laboratory notebook and authors reports as assigned

– Designs, executes, and interprets experiments with a high degree of reliability and independence

– Performs basic statistical analysis of experimental data, where appropriate

– Maintains general lab equipment, including HPLCs and dissolution systems.

– Demonstrates knowledge of scientific principles and basic understanding of applicable drug development regulations

– Performs other duties as assigned

Minimum Qualifications:

– A Bachelor’s degree degree in Chemistry, Chemical Engineering or Pharmaceutical Chemistry and 0-2 years relevant analytical experience

– Knowledge of HPLC and dissolution testing is required

– Excellent experimental documentation is required

Preferred Qualifications:

– A basic knowledge of cGMPs is required

– Dissolution experience across multiple systems (manual, semi-automated and automated dissolution systems)

– Experience with biorelevant dissolution testing

– The ability to work successfully in both a team/matrix environment as well as independently

– The ability to work in a fast pace environment, manage priorities, and maintain timelines for multiple projects

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