Description
The company
The Harvey Nash Group was founded in the UK in 1988, and now has offices throughout Europe, America and Asia. The Harvey Nash Group is known for the thousands of successful assignments completed throughout the world.
From more than 39 offices, and with 5000 staff and associates, we offer a unique range of consulting recruitment specialising in IT & Engineering recruitment, benefits subcontracting and outsourcing services to our clients. Our departments of Executive Search and Interim Management support our customers around the world by placing the senior managers essential to business growth and effective management.
For our client we're actively looking for an "Regulatory Affairs Registration Manager".
Function Description
One RA professional is required. Daily tasks will be related to the regulatory management of products (Vaccines). Role will be to project manage filing of variations worldwide including Europe and resolve supply related issues. It may involve both maintenance of dossiers as well as new dossier submissions. The person will be required to communicate both internally and externally, and maintain and update various databases and planning tools associated with the role.The positions will be initially for a six month period and would be based in Wavre, Belgium.
Prerequisites
Education: University degree (preferably biological/chemical)
Knowledge:
Knowledge of Regulatory legislation in at least one geographic areaBasic understanding of biologicals/vaccines
Experience:
Ideally more than 4 years experience in the pharmaceutical industry; this should include at least 3 years RA experience.
Proven ability to manage typical regulatory activities, resolve problems and deliver results