...regulatory authorities) on defined matters.
·
Face external audits / inspection, coordinate and communicate with external auditors / inspectors for compliance.
Qualifications
Expertise in regulatory compliance ...
Name of the Company: Move Ahead Consultancy
Location: U.S COMPLEX, Office No. 212, Second floor, Jasola, New Delhi-110076
Designation: Executive/Senior Executive –Regulatory Affairs Work Experience: 0 to 5 years
Qualification: MSc. /B.Tech, M...
Designation:
Manager – Distributed Renewable Energy Practice
Location:
Delhi
Educational Qualification:
BE – Electrical / Mechanical and MBA / MS / M.Tech
Experience:
6 - 7 years (2-3 years prior experience of management consultancy would ...
Company Description
Aimlay is a global educational and writing service platform for working professionals. The company offers a vast array of courses, including Ph.D. programs, in collaboration with renowned universities across India. Aimlay's goal i...
Job description
The Regulatory Affairs team is responsible for ensuring our products meet legislative
requirements, and that the public's health is protected by controlling the safety and efficacy of these products Our RA team keeps track of the ever...
Description Public Policy Manager
The Private Office is a leading boutique advisory firm specialising in providing confidential and strategic legal and tax-related services to a select clientele. We focus on delivering bespoke solutions that addre...
We are Archetype
Setting the standard for the next generation of global agencies, Archetype partners with category creators and industry leaders to build the world’s most magnetic brands. We are 650 curious and creative individuals in 20 offices arou...
Job description
The objective of Government Affairs function is to represent B Braun by managing and supporting market access of our innovative medical technologies and drugs and contributing to the development of sustainable health care systems....
...regulatory requirements at GPC Medical.
Roles and Responsibilities
· Prepare and update technical documentations as per EU MDR and 510 (k) regulatory requirements as required.
· Prepare and update risk management...
