Description
- Sound knowledge of relevant Regulatory & Quality Standards. Experience of direct interaction with US FDA, EU Competent Authorities and Notified Bodies.
- Ability to build relationships quickly with a diverse range of colleagues at all levels in the organisation including key stakeholders.
- Ability to work effectively and collaboratively across the organisation.
- Ability influence others without having formal authority over them.
- Ability to coordinate and synchronize multiple projects and be flexible in changing daily workload priorities.
- Self-motivated individual who can work independently or with a team and meet deadlines.
- Excellent organisational / planning and negotiation skills.
- Ability to think about Regulatory Affairs strategically in terms of the Company's mission, vision and goals.
To find out more about Real please visit www.realstaffing.com