Description
A market leading client in Massachusetts is urgently seeking Regulatory Affairs Project Managers.An ideal candidate will have:
- 7+ years of experience as a Project Manager
- Experience working directly within an organization responsible for global licensing and registration inform ation process
- Pharmaceutical, Bio-Technology, or Life Science industry experience
- Experience working in a GxP validation environment
- Systems Development Life Cycle (Analysis through Implementation)
- Experience with Regulatory Processes and Systems a plus
- Experience with industry leading registration management tools.
o Liquent (essential)
o Trackwise / quality
o ARIS Global (RM components)
o Oracle / Supply Chain
- Experience with secondary registration management tools
o SAP
o Register
- Awareness of Business and Enterprise Architecture
- Strong Customer and Business Relationship Management skills
- Project experience with COTS and web application requirements, design, or development
If you are interested, please send an updated CV and I would be happy to discuss the position further.
Thank you!