Process Executive (Regulatory Compliance – Medical Devices) at Cognizant

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