Takeda Pharmaceuticals Int'l Co Work Values

Daily Duties at Takeda Pharmaceuticals Int'l Co:

Executed cGMP batch manufacture of Takeda’s anticancer drugs Velcade, Mepact and Adcetris (an ADC) at 4 major CMOs for late-stage clinical evaluation, commercial launch and product quality lifecycle management.

What they like about Takeda Pharmaceuticals Int'l Co:

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 Takeda Pharmaceuticals Int'l Co: