With a focus on electrification, automation and digitalization, Siemens India stands for engineering excellence, innovation, and reliability. As one of the world’s biggest producers of energy-efficient, resource-saving technologies, Siemens is a pioneer in infrastructure and energy solutions, automation and software for industry and is a leader in medical diagnosis. Siemens also provides business-to-business financial solutions, rail automation and wind power solutions.
Post : Regulatory Affairs Professional
Job Description
• This recruitment is for getting a replacement as the current incumbent has resigned.
• This position is primarily responsible to ensure pre market & post market compliance to Medical Device Rules(MDR) 2017 governed by Central Drug Standard Control Organization (CDSCO) for SHPL's IVD & other medical devices to be sold in India.
• This is PL7 grip level position.
Pls. look for candidates for his position Regulatory professional (PL7) – B-Pharm/ M-Pharm with 8-10 years experience of pre market & post market work on compliance to Medical Device Rules(MDR) 2017 governed by Central Drug Standard Control Organization (CDSCO) for SHPL's IVD & other medical devices.
• We would need to have the replacement candidate on board by first week of July’19.
Additional Information
Experience : 8-10 years
Qualification : B.Pharm, M.Pharm
Location : Gurgaon, India
Industry Type : Pharma/ Healthcare/ Clinical research
Functional Area : Regulatory Affairs
Req ID : 113737
End Date : 20th June, 2019
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