Description
Regulatory Affairs Project ManagerMy client, a global biotechnology company is looking for a Regulatory Affairs Project Manager. This company's products help millions of people around the world who are fighting against serious illnesses such as kidney disease and cancer.
The regulatory affairs project manager will be working in conjunction with the regulatory affairs manager to assist in submissions and transferring products from various other sites. As regulatory affairs project manager you will be managing the transfer of 7 products to the Irish site in Dublin. You will be dealing with high level projects and will need global submissions experience.
Your tasks:
Submissions to global regulatory authorities
Work closely with national and international authorities
Understand the current and future new product launches and create overview landscape, then maintain.
Ensure project documents are complete, current, and appropriately stored.
Work closely with relevant stake holders to ensure effective and efficient implementation of the new project launches.
Your profile:
Strong experience pharmaceutical Regulatory Affairs application
Experience in the field of national and international approval for
pharmaceuticals
Knowledge of relevant standards, laws and regulations
Fluent English skills
Able to work to and deliver on deadlines
Understand global regulatory strategy
Previous experience as a regulatory project manager
Understanding of biologics
Experience in dealing with testing implications on a global scale (particularly middle east)
An excellent salary plus a very attractive benefits package is on offer. This is an urgent requirement so interviews will be immediate. If you are interested in this great opportunity please contact me Laura Watson on and click apply with an updated CV for immediate consideration. To find out more about Real please visit www.realstaffing.com
To find out more about Real please visit www.realstaffing.com