PAREXEL has supported the Bio-Tech and Pharmaceutical industries in helping the development of new drugs and treatments on a global basis. As a leading global biopharmaceutical service provider, they supply knowledge-based contract research, medical communications and consulting services across a broad range of therapeutic areas to the worldwide pharmaceutical, biotechnology and medical device industries.
Post : Senior Regulatory Affairs Associate
Job Description
1. 5-8 years of CMC regulatory experience.
2. Understanding of global regulatory requirements
3. Preparation, compilation and submission of product registration dossiers to HA in required format
4. Good review skills of submission package
5. Have worked on post approval changes specifically for EU countries
Candidate Profile
1. M.Sc/M.Pharm in life Science
2. Should be willing to work in 12:30-9:00 pm shift
3. Client focused approach
Additional Information
Job ID : 55902BR
Qualification : M.Pharm, M.Sc
Location : Bengaluru, Karnataka
Industry Type : Pharma / Healthcare / Clinical research
Functional Area : Regulatory Affairs
End Date : 11th December, 2019
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