Quality & Regulatory manager_Reputed Medical Device Industry_15 LPA

Seven Consultancy; Davanagere; On-site; INR 1,800,000 - 3,200,000; Full time

Job summary

Seven Consultancy in Karnataka, Davanagere, India seeks a senior Quality/Regulatory professional with a minimum of 10 years' experience in quality and/or regulatory roles within the medical device industry. Strong knowledge of ISO 13485, FDA 21 CFR Part 820, EU MDR, CDSCO and related standards is essential. Experience preparing regulatory submissions is required.

This role is categorized under Quality Assurance - Other. UG graduates are eligible.

Qualifications

• Minimum 10 years' experience in quality and/or regulatory roles in the medical device industry.
• Strong knowledge of ISO 13485, FDA 21 CFR Part 820, EU MDR, CDSCO and related standards/regulations.
• Experience preparing regulatory submissions.

Education

Any Graduate

Job description

Minimum 10 years' experience in quality and/or regulatory roles in the medical device industry.

Strong knowledge of ISO 13485, FDA 21 CFR Part 820, EU MDR, CDSCO and related standards/regulations.

Experience preparing regulatory submissions.

Role Category: Quality Assurance - Other

Education

UG: Any Graduate

Key Skills

Skills highlighted with ' are preferred keyskills