4 Job openings found

1 Opening(s)
10.0 Year(s) To 25.0 Year(s)
30.00 LPA TO 35.00 LPA
Experience: 10+ years of experience including team handling experience in similar domain Location: Ahmedabad, Gujarat   Summary of Profile specifications:   Incumbent should have sound knowledge of domestic regulatory functions with ref to DBT-RCGM, CDSCO and state FDA regulations.  He/she should be a seasoned professional with leadership qualities, have knowledge about NDCT rules, Biosimilar guidelines, cGMP ...
1 Opening(s)
12.0 Year(s) To 15.0 Year(s)
Not Disclosed by Recruiter
Ensure regulatory compliance data execution for the Region.• Ensure regulatory compliance and effective communication to all stakeholders (e.g. PS (Product Stewardship) Region Heads and teams, any other PS department, Business Unit interfaces, Procurement etc.)• Align team goals with PS (Product Stewardship) global targets while adhering to Clariant values.• Drive continuous ...
1 Opening(s)
14.0 Year(s) To 25.0 Year(s)
30.00 LPA TO 65.00 LPA
KEY RESPONSIBILITIES Responsible for leading the design, implementation, and maintenance of comprehensive security measures across all stages of medical device development, ensuring compliance with relevant regulations and standards while protecting patient data and device integrity Lead the design and implementation of secure architectures for new medical devices, considering connectivity, data protection, access ...
1 Opening(s)
4.0 Year(s) To 8.0 Year(s)
9.00 LPA TO 13.00 LPA
Purpose of the Job identify existing deviations, take corrective actions and prevent recurrence. Take pro-active actions to Quality Assurance aspects. Drive improvement projects. Requirements: Education - Degree in Engineering or Software (e.g. mechanical engineering, electrical engineering, industrial engineering) Work Experience: Minimum 5 years of professional experience, preferably in the Medical Device industry Experience in Quality Assurance, Regulatory Affairs, ...

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