Aegis Lifesciences Pvt Ltd Hiring for Regulatory Affairs Professionals.
Title/Designation: Executive- Regulatory Affairs
Department – Regulatory affairs
Industry – class III Medical Device
Educational Qualification – M Pharma, B pharm or Msc
Job description :-
Executive- Regulatory Affairs
An exciting opportunity to work for class III / Class-D medical device certification & regulations
Key responsibilities/ accountabilities:
For the above position, your roles and responsibilities would include:
- To assist in new products registration and license renewal compliance to local regulations, as well as GMP, CE and ISO 13485 requirement.
- To assist the QA/RA team and ensure quality and good standard operating procedures within the company.
- Have the joint responsibility to develop, facilitate and execute comprehensive regulatory strategies through all phases of development and product life cycle, to accelerate and ensure successful product registrations and provides regulatory assessment and supports Change Control Assessment.
- Oversee the maintenance of product quality and compliance through the Quality Assurance and Quality Control functions as well as management of the Quality Management System and compliance processes.
Office & Factory Address :
AEGIS LIFESCIENCES PVT LTD
215/216, Mahagujarat Industrial Estate, Sarkhej-Bavla Road, At: Moraiya, Po: Changodar, Ta: Sanand
Desired Skills and Experience
class III Medical Device, Regulatory Affairs, Quality Assurance.
Application Process :-
Pl send your cv to E-mail: firstname.lastname@example.org
Check Below Link