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Regulatory Affairs, Pharma, Kandivali - Mumbai @ VHB Medi Sciences

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 Regulatory Affairs, Pharma, Kandivali - Mumbai

Job Description

Planning, execution& submission of dossiers to ROW Markets. Interacting with regulatory authorities for approval of new/existing applications. Co-Ordination with R & D team for setting specifications etc, Packaging Development to plan new art works

Required Candidate profile

Candidate should be B.Pharm/M.Pharm in Regulatory Affairs with 3 to 7 years experience in reputed Pharma Formulation manufacturing Company.
Experience of handling ROW markets in Pharma Company is required.
Can Handle Target and complete dossiers.

Perks and benefits

As per Company Norms

Job Classification

Industry: Pharma, Biotech, Clinical Research
Functional Area: Medical, Healthcare, R&D, Pharmaceuticals, Biotechnology,
Role Category: Drug Regulatory Affairs/Documentation
Role: Drug Regulatory Affairs/Documentation
Employement Type: Full time

Education

Under Graduation: B.Pharma
Post Graduation: M.Pharma
Doctorate: Doctorate Not Required, Any Doctorate in Any Specialization

Contact Details:

Company: VHB Life Sciences Limited
Location(s): Mumbai
Website: http://www.vhbgroup.com/

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Keyskills:   ctd dossiers regulatory affairs officer regulatory regulatory affairs dossier row manager regulatory affairs

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VHB Medi Sciences

Pharma Manufacturing