Dune Medicare is a Danish generic marketing company developing and manufacturing generic medicinal products for the European Marked.
Post: Head of EU Regulatory
Job Description:
Dune Medicare is presently in search of a regulatory affairs head for development of CTD’s for the Scandinavian market. We expect that you have a minimum experience of 15-20 years in CTD development and further have adequate management & leadership skills.
Your responsibilities will cover development of generic equivalents from lab scale to commercial production as well as development of data for eCTD’s and training of junior staff members. Further, you will be responsible for planning and initiation of bio-equivalence studies for developed finished dosage formulations.
Candidate Profile:
They expect that you are a M.Pharm or M.sc. graduate with thorough experience in CTD development. In addition you are required to have sufficient leadership skills and understand the basic concept of strategic planning.
Additional Information:
Experience: 15-20 Years
Location: Mumbai
Education: B.Pharm, M.Pharm, B.Sc, M.Sc
Industry Type: Pharma/ Biotech/Clinical Research
Functional Area: DRA
End Date: 19th Oct., 2011
Forward Your Resume at, vacancy@dunemedicare.com
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