Looking to build a career in medical device regulatory affairs jobs in India? Here’s a strong opportunity with Cognizant for a Senior Process Executive (Regulatory Compliance – Medical Devices) role. This position is ideal for candidates with 1–4 years of experience in regulatory compliance, audits, and quality systems, especially those familiar with FDA, ISO 13485, and MDR regulations.
This role offers hands-on exposure to global regulatory compliance processes, making it a valuable step for professionals aiming to grow in medical device regulatory affairs careers.
Job Overview
- Position: Senior Process Executive (Regulatory Compliance – Medical Devices)
- Company: Cognizant
- Experience: 1–4 Years
- Qualification: Life Sciences / Pharmacy / Biomedical Engineering
- Location: India (Hybrid/Office-based depending on project)
- Industry: Medical Devices / Regulatory Affairs / Compliance
Key Responsibilities
- Ensure compliance with global regulatory standards including FDA, ISO 13485, and MDR
- Manage regulatory documentation, records, and compliance reports
- Support audits, inspections, and regulatory reviews
- Collaborate with Quality Assurance (QA), Regulatory Affairs (RA), and Operations teams
- Monitor and track regulatory updates and industry trends
- Assist in risk management and quality system processes
- Identify compliance gaps and drive continuous improvement initiatives
Eligibility Criteria
- Bachelor’s degree in Life Sciences, Pharmacy, Biomedical Engineering, or related field
- 1–4 years of experience in medical device regulatory compliance or regulatory affairs jobs
- Strong background in documentation, audit support, and compliance processes
Preferred Skills
- CAPA (Corrective and Preventive Actions)
- Risk Management in medical devices
- Audit handling and inspection readiness
- Regulatory submissions knowledge (FDA, MDR)
- Experience with compliance tracking tools
Key Competencies
- High attention to detail
- Strong communication and stakeholder management
- Analytical thinking and problem-solving ability
- Ability to work in a fast-paced regulatory environment
Salary & Benefits
- Estimated Salary: ₹3,50,000 – ₹7,50,000 per annum
- Opportunity to work on global regulatory compliance projects
- Exposure to international medical device regulations
- Career growth in regulatory affairs and quality assurance
- Learning and development within a leading global organization
How to Apply
Interested candidates can apply by sending their updated CV to:
📩 debasmita.r@2coms.com
Make sure your resume highlights:
- Regulatory compliance experience
- Audit and documentation expertise
- Knowledge of FDA, ISO 13485, MDR
Mention Subject : Pharmabharat Candidate for medical Devices