Work from Home Regulatory Affairs Specialist Hiring Medtronic
Work from Home Regulatory Affairs Specialist Hiring Medtronic
Join Medtronic as a Regulatory Affairs Specialist | Hybrid Opportunity
Are you an experienced Regulatory Affairs Specialist looking for a career opportunity with a global healthcare leader? Medtronic is currently hiring for a Regulatory Affairs Specialist (Level II) in Hyderabad, India, with the flexibility of a hybrid work-from-home arrangement. This is a fantastic opportunity to work with a renowned medical technology company and contribute to regulatory compliance and innovation in healthcare.
Job Details
• Company: Medtronic
• Position: Regulatory Affairs Specialist – II
• Vacancies: 2
• Work Type: Hybrid (Work from Home + Office)
• Location: Nanakramguda, Hyderabad, India
• Employment Type: Full-time
Roles & Responsibilities
As a Regulatory Affairs Specialist, you will:
• Support design and development control activities with regulatory strategies and requirements.
• Prepare, review, file, and support premarket regulatory documents for global product registrations.
• Collaborate with business units and international regulatory teams to obtain marketing approvals.
• Review pre-clinical and clinical protocols to ensure compliance with regulatory standards.
• Develop regulatory strategies for new or modified medical devices.
• Maintain oral and written communication with health authorities.
• Participate in regulatory inspections and audits.
• Review and assess change control documents to determine regulatory impact.
• Ensure compliance with India CDSCO, US FDA, and EU MDR regulatory frameworks.
Qualifications & Experience Required
Minimum Qualifications:
Education: Bachelor’s or Master’s degree in:
• Life Sciences (BSc, MSc)
• Pharmacy (B. Pharm, M. Pharm)
• Medical, Mechanical, Electrical Engineering
Experience:
• 4-7 years of regulatory affairs experience in the medical device or pharmaceutical industry
• Strong knowledge of India CDSCO, US FDA, and EU MDR regulations
• Experience with regulatory submissions and product approvals
• Excellent written and verbal communication skills
Preferred Qualifications:
• Global regulatory affairs knowledge and experience.
• Experience working with cross-functional teams.
• Strong problem-solving and project management skills.
• RAPS Regulatory Affairs Certification (RAC) is a plus.
• Ability to work under tight deadlines and pressure.
[caption id="attachment_121768" align="aligncenter" width="1200"] Work from Home Regulatory Affairs Specialist Hiring Medtronic | Apply Now[/caption]
How to Apply?
Interested candidates can apply directly through Medtronic’s career portal: Apply Here
Application Deadline: Open until filled
Apply Now
Join Medtronic as a Regulatory Affairs Specialist | Hybrid Opportunity
Are you an experienced Regulatory Affairs Specialist looking for a career opportunity with a global healthcare leader? Medtronic is currently hiring for a Regulatory Affairs Specialist (Level II) in Hyderabad, India, with the flexibility of a hybrid work-from-home arrangement. This is a fantastic opportunity to work with a renowned medical technology company and contribute to regulatory compliance and innovation in healthcare.
Job Details
• Company: Medtronic
• Position: Regulatory Affairs Specialist – II
• Vacancies: 2
• Work Type: Hybrid (Work from Home + Office)
• Location: Nanakramguda, Hyderabad, India
• Employment Type: Full-time
Roles & Responsibilities
As a Regulatory Affairs Specialist, you will:
• Support design and development control activities with regulatory strategies and requirements.
• Prepare, review, file, and support premarket regulatory documents for global product registrations.
• Collaborate with business units and international regulatory teams to obtain marketing approvals.
• Review pre-clinical and clinical protocols to ensure compliance with regulatory standards.
• Develop regulatory strategies for new or modified medical devices.
• Maintain oral and written communication with health authorities.
• Participate in regulatory inspections and audits.
• Review and assess change control documents to determine regulatory impact.
• Ensure compliance with India CDSCO, US FDA, and EU MDR regulatory frameworks.
Qualifications & Experience Required
Minimum Qualifications:
Education: Bachelor’s or Master’s degree in:
• Life Sciences (BSc, MSc)
• Pharmacy (B. Pharm, M. Pharm)
• Medical, Mechanical, Electrical Engineering
Experience:
• 4-7 years of regulatory affairs experience in the medical device or pharmaceutical industry
• Strong knowledge of India CDSCO, US FDA, and EU MDR regulations
• Experience with regulatory submissions and product approvals
• Excellent written and verbal communication skills
Preferred Qualifications:
• Global regulatory affairs knowledge and experience.
• Experience working with cross-functional teams.
• Strong problem-solving and project management skills.
• RAPS Regulatory Affairs Certification (RAC) is a plus.
• Ability to work under tight deadlines and pressure.
[caption id="attachment_121768" align="aligncenter" width="1200"] Work from Home Regulatory Affairs Specialist Hiring Medtronic | Apply Now[/caption]
How to Apply?
Interested candidates can apply directly through Medtronic’s career portal: Apply Here
Application Deadline: Open until filled
Apply Now