Analyst at Genzyme around pharmaceutical analytical laboratory doing numerous analytical techniques for raw materials, API in addition to finished product. Method verification, shift plus validation.
Past practical experience as analyst for your chromatography party in just Analytical Services at Par Pharmaceuticals.
Past knowledge since analyst for just a chromatography number within Analytical Quality Sciences division at Wyeth with eighteen many experience.
Experience with: - cGMP research connected with pharmaceutic materials simply by many chromatography techniques including GC, HPLC, GC/MS, dissolution, TLC, in addition to KF. Support with tasks from pre-IND to be able to NDA submission. - Specifications and analysis regarding meds resources determined by USP as well as ICH suggestions - Coordinating method qualification/validation tasks to get Regulatory Submissions. - Coordinating method specialised transfers to central sites plus post paid laboratories.
Project company direction for in-house drug compound. Duties will be to be able to represent analytical from group meetings, submitting in addition to publishing regarding selections regarding this venture and also presenting analytical data during central task evaluation meetings.
SpecialtiesSpecialties are given while in the over practical knowledge in addition to goals section.
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