Ariad Pharmaceuticals Inc Work Values

Daily Duties at Ariad Pharmaceuticals Inc:

As QA technical lead, collaborated with CMC process chemistry on analytical method transfer, process validation and cGMP manufacture of API and DP, supporting Ariad’s late-stage small molecule anticancer drug development programs.

What they like about Ariad Pharmaceuticals Inc:

Organizations with strong, centralized leadership are particularly attractive to you. You require a work environment with leadership that aggressively seeks to expand and grow the business and does so in a visible and decisive manner. In general you prefer to work in an environment in which there is a strong link between leadership, its actions, and a strong set of company-wide values.

Tags

Chemical Process Development, API, cGMP Manufacture, Technology Transfer, Management, Quality, Risk Assessment, Pharmaceutical Operations, FDA and ICH Drug Regulations, CRO, CDMO and CMO Oversight, CMC Process Chemistry, TrackWise QMS, Change Controls, Deviation Management, Investigations, Root Cause Analysis, CAPA, Antibody Drug Conjugates, IND, IMPD, NDA, MAA and BLA

Skills

CMO CDMO Management, Matrix Project Management, QC and QA, Quality Risk Assessment, TrackWise QMS, cGMP Compliance, TrackWise QMS, Clinical Batch Manufacturing, QC and QA, Deviation Management and Investigations, Root Cause Analysis and CAPA, CMC Process Chemistry and Development, Six Sigma Green Belt and RAC Certified, Six Sigma Green Belt and RAC Certified, Technical Writing, API, Drug Substance and Drug Product, Quality by Design

These are some of the questions we asked our climbers about their experiences with Ariad Pharmaceuticals Inc: