Description
I am working on a very exciting position that has just become available, as a Senior Regulatory Affairs Officer, in a leading Pharmaceutical Company.
The company manufactures and distributes cost conscious medicines to the UK & global market.
The position is available immediately, you will be based in Hampshire & the role is for a 3 month contract with the possibility to extend & offering competitive rates.
The role will include:
-Production and review of Design Dossiers, Technical Files and Product Master Files
-Preparation of regulatory submissions for product approvals/registrations
-Participation in Quality Audits and supporting QA manager in ensuring readiness for audits
-Communicating with outside agencies/regulatory bodies
For this role you will ideally have the following experience:
-Regulatory Affairs experience within a generic pharmaceutical environment
-Excellent attention to detail
-Be able to work on own initiative & unsupervised
-Microsoft Word and Excel experience
-Renewal of drug licencing
-Type-II variations experience
-Experience of working with the MHRA
-Excellent communication and interpersonal skills
For more information on this great opportunity, please reply to this advert or contact Richard Williamson.
Lawrence Harvey is acting as an Employment Business in regards to this position.