Title: Sr. Analytical Scientist Location: Research Triangle Park, NC Duration: 12+ months Rate: $Open/hr. Requirements General Responsibilities: + Plan and conduct analytical tests for drug development and transfer the methods to CDMO + Analyze and interpret data and prepare technical reports + Perform IQ/OQ/PQ and maintain lab equipment + Follow safety procedures and good laboratory practice + Must be able to work independently with limited guidance from external consultants or CEO (this role would report directly into the CEO). + BS/MS with 10-12+ years of pharma industry analytical experience working within analytical development/validation to support solid oral dosage forms (small molecules), Ph.D. with 5-7+ years. + Excellent method development and validation skills and routine analysis on pharmaceutical materials (including potent compounds). + Strong preference for an analytical scientist who has used a variety of analytical techniques/instrumentation – for example, particle size analysis, TGA, DSC, HPLC, FTIR, Powder XRD, SEM, HPLC (Agilent), Dissolution, UV-Vis. + Strong preference for an analytical scientist who either has worked within a contract analytical lab working with external clients or has worked within a pharma company who outsourced some analytical work to external CDMOs. + Ability to self-manage and take on new tasks + Ability to learn new analytical techniques by hands-on work and review of published data + Ability to multi-task and hit project timelines. + Excellent oral and written communication skills + ANDA background a plus. Benefits Note: If interested please send your updated resume to joseph.prabakar@two95intl.com and include your salary requirement along with your contact details with a suitable time when we can reach you. If you know of anyone in your sphere of contacts, who would be a perfect match for this job then, we would appreciate if you can forward this posting to them with a copy to us. We look forward to hearing from you at the earliest!