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 : Manager Regulatory Affairs
Job Responsibilities
- The candidate should be well versed in Regulatory Affairs with good experience in CMC, MAT, post approval maintenance activities like renewals, variations, annual reports, change control pertaining to EU and US markets.
- He should be very good in communication and writing skills and should be able to lead and train junior colleagues.
- Experience in effectively dealing and interacting with clients will be an added advantage.
Candidate Profile
M.Sc./M.Pharma/ B.Tech with 10-12 years of relevant experience in dealing with Regulatory submissions with at least 3-4 years of experience of managing and handling team.
Additional Information:
Experience: 10-12 years
Location: Bengaluru
Education: M.Sc, M.Pharm
Industry Type: Pharma/ Biotech/Clinical Research
Functional Area: Regulatory Affairs
End Date: 24th February, 2018
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