Pine Brook, New Jersey
Independently authors, compiles, reviews, and schedules high-quality regulatory submissions in adherence with standards that are fully compliant with FDA and ICH requirements within company timelines. Submissions will include: ANDAs, NDAs, ...
26d
| Job Type | Full Time |
Associate/Sr. Associate Regulatory Operations, CMC
Pine Brook, New Jersey
This position is primarily responsible to plan, coordinate and prepare regulatory submissions in adherence with technical document standards that are fully compliant with FDA and ICH requirements. Serve as a primary publisher of US Regulato...
26d
| Job Type | Full Time |
Houston, Texas
Are you interested in joining our team? Chat with our digital assistant to learn more about our company and apply right from your mobile device! Text ETP to 25000 to get started or apply through this web posting if you prefer. Energy Transf...
26d
| Job Type | Full Time |