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:

You give high priority to hiring firms with prestige. Market reputation and prestige of a firm may be determined through on-line research, and conversations with individuals working in your target industry. Note that firms "in the public eye" receive a great deal more critical publicity and attention than those operating with more anonymity. So as you assess your employment opportunities, be sure to seek out the positive aspects of the firm's reputation in addition to noting negative publicity the company may have received.

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: