Tedor Pharma Work Values

Daily Duties at Tedor Pharma:

Manage project and interface with various partners across the organization; Coordinate analytical work as a project leader; Take part in pre-formulation self guided discovery work; Developed, validated analytical methods for pharmaceutical finished products; Compile analytical method and protocol. Perform document change control. Assist in FDA filings. Stay current with new technology and new regulatory requirements by frequenting 3 to 5 websites

What they like about Tedor Pharma:

The social vibrance of a hiring firm is very important to you. Your ability to make and maintain friendships there is a critical part of your decision. You would likely be dissatisfied with a workplace that is quiet, cold, or otherwise not particularly social. When you investigate a new hiring company, ask recruiters, managers, and potential co-workers about the social life and opportunities there. This is especially important when you are relocating; moving dramatically alters your social sphere both inside and outside the workplace.

Tags

Pharmaceutical Analysis, Development, Validation, Rhode Island, Florida, Texas, Method Transfer

Skills

• Pharmaceutical analysis, • Leadership attributes, • Polymer synthesis, • Organic synthesis, • Environmental analysis, • USP/EP, • ICH guidelines, • ISO9001, • cGMP, • SOP, • DEA, • OSHA, • Method development, • Method validation, • Method transfer, • Impurities, • HPLC, • GC, • UV/Vis, • IR, • KF, • DSC, • Dissolution, • Viscometer, • Atomic absorption, • Malvern 2000, • Ion chromatography, • Solid phase extraction, • MS, NMR

These are some of the questions we asked our climbers about their experiences with Tedor Pharma: