Job Description
Provides appropriate regulatory and technical services, complies with company's policies, EU and local laws and guidance, as necessary for the company's activities worldwide
Responsible for maintenance of marketing authorisations, clinical trial approvals and wholesales dealers licences by submission of appropriate variations and renewals
Responsible for contract with regulatory authorities and follow up if necessary
Responsible for customer complaint procedures
Ensures compliance of artwork for marketed products

Candidate Profile
University degree in pharmacology, life sciences, chemistry or similar
Postgraduate studies will be considered as an asset
Three (3) - five (5) years of working experience in regulatory affairs from a generics pharmaceutical company
Proven work experience in the full range of regulatory activities (preparation of product submissions, life-cycle management etc) and in liaison with world-wide Medicines Agencies
Excellent knowledge of European Union framework
Excellent command of the english and greek language
Pc literacy
Problem solving, analytical and team work skills
Communicative and organizational skills

The Company Offers
Competitive remuneration package
Mobile phone
Bonus scheme

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