Are you the superhero that is going to make a difference for the patients?
Role DescriptionAs a new employee you will manage changes specific to GMP/GDP. Also will you coordinate the GXP RIN program. You will be responsible for the contact with the stakeholders and experts internally and externally of our client.
ResponsibilitiesYour responsibilities are as followed: - Be an internal consultant for key regulatory topics - Editing GMP/GDP content - Be the GMP/GDP RIN leader and work wih the other leaders. - Managing GMP/GDP/Device/CMC - Developing and executing tools
RequirementsTo be a part of this amazing team and company you need to have: - Strong organizational and project management skills - Fluent English is a must - High degree of independence - Minimum 8 years working in the life science industry - Minimum 5 years working in quality assurance - Experience with GMP regulation
Other informationAre you the hero they need? Apply and try!
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Diana Prieto Reyes.