- 12years of regulatory experience in medical device industry (equivalent industry/educational experience may be considered)
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Regulatory Affairs
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Regulatory Affairs
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Statistical Pharma Pune, IndiaThe **Regulatory Affairs Specialist** stays with the same company for an average of 10 to 15 years; the rate of turnaround is therefore low. Networking is very much encouraged, through joining various associations to participate in conferences and exhibitions, and also to access ...
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Liquidity Measurement Reporting, Eno
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Quality Partner
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Liquidity Measurement Reporting, Eno
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Liquidity Reporting, Avp
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Liquidity Measurement Reporting, Eno
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Liquidity Measurement Reporting Avp
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Credit Suisse Pune, India**Your field of responsibility** · Join us as an AVP - Regulatory Reporting Specialist in the Liquidity Reporting function. Your responsibilities include preparing, analyzing and reviewing liquidity reports prior to submission to global regulators. You participate in projects, ne ...
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Regulatory Specialist - Pune, India - Cyient
Description
Designation :
Regulatory Specialist
Experience : 7+
Location :
Pune
Qualifications
Bachelor of Science in science and/or engineering field
Experience in Orthopedics industry preferred.
510(k) experience and Regulatory Affairs Certification (RAC) preferred.
Ability to work under limited supervision with FDA, Notified Body, Authorized Representatives, 3rd party license holders and other global regulatory agencies.
Ability to support and execute activities related to product development teams and cross-functional projects.Ability to work well with others and manage projects.
Excellent written and verbal communication skills. Proficient in Microsoft Office
Ability to read and speak English sufficiently to read, understand, and complete all documentation.
Mandatory Skills
Medical Device Regulations,FDA Medical Device Regulations,Regulatory Compliance,Medical Devices,Cross-Functional Teamwork