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)
11.0 Year(s) To 18.0 Year(s)
23.00 LPA TO 50.00 LPA
jD:
Serve as the company’s subject matter expert on drug safety and pharmacovigilance
Ensure compliance with Local & Global PV-relevant Heath Authority requirements
Oversee PV Contracts, vendor management and PV system audits/inspections
Have good understanding of signal management and benefit-risk evaluation activities
Develop and implement Risk Management Plans (RMPs) and additional Risk mitigation measures
Act as the primary safety liaison with country regulatory authorities ...
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, ...