Epix Pharmaceuticals Inc. Work Values

Daily Duties at Epix Pharmaceuticals Inc.:

Oversaw multiple CDMOs in the US, UK, Canada, India and Japan, directing CMC regulatory, cGMP, QC and QA functions of 5 novel small molecule drugs developed for major depressive disorder, Alzheimer’s disease, obesity, PAH, COPD and IBS. Managed the work of 25-30 chemists at external CROs|CDMOs|CMOs and accomplished a large number of matrix projects, working closely with cross-functional project teams.

What they like about Epix Pharmaceuticals Inc.:

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

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 Epix Pharmaceuticals Inc.: