Analyst at Genzyme in pharmaceutical analytical laboratory performing multiple analytical strategies regarding raw materials, API in addition to finished product. Method verification, transfer and validation.
Past experience as analyst for just a chromatography group inside Analytical Services with Par Pharmaceuticals.
Past experience as analyst for just a chromatography group within just Analytical Quality Sciences split at Wyeth along with eighteen years of experience.
Experience with: - cGMP examination with pharmaceutical drug supplies by means of several chromatography procedures such as GC, HPLC, GC/MS, dissolution, TLC, and also KF. Support of projects from pre-IND to NDA submission. - Specifications plus examination associated with medicine supplies determined by USP in addition to ICH tips - Coordinating process qualification/validation projects for Regulatory Submissions. - Coordinating system complex transfers for you to bodily web-sites in addition to deal laboratories.
Project crew management to get in-house medicine compound. Duties are usually to characterize analytical at workforce meetings, applying and releasing connected with selections in connection with this project as well as giving a presentation analytical information at central task review meetings.
SpecialtiesSpecialties tend to be granted inside the actual on top of practical experience and objectives section.
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