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. They have helped over 800 clients to develop and launch some of the most important drugs and devices of our time-helping people live better and healthier lives everywhere in the world. Headquartered near Boston, Massachusetts, PAREXEL operates in more than 50 countries around the world.
Post : Regulatory Affairs Associate
Job Description
Candidate should have 3 to 5 years of experience in regulatory affairs with core area of experience in CMC. He or sheshould have experience in post approval CMC Submissions, compiling and review of post approval submissions globally including variation, renewals and safety reports. He or she should be well versed with post approval change control assessments.
Candidate Profile
First class Graduate/Post Graduate in Life Sciences/ Pharmacy with relevant work experience (RA) for 3-5 years in the reputed organizations.
Additional Information:
Location: Bengaluru, Karnataka, India
Education: M.Pharm, M.Sc, B.Pharm, B.Sc
Industry Type: Pharma/ Biotech/Clinical Research
Functional Area: Regulatory Affairs
End Date: 20th January, 2019
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