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Manager - Regulatory Affairs (Gurgaon)

Fresenius Medical Care
Fresenius Medical Care
8 years
Not Disclosed
Gurugram, Haryana, India
10 Feb. 26, 2026
Job Description
Job Type: Full Time Hybrid Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Manager – Regulatory Affairs & Quality Assurance (Medical Devices & Pharmaceuticals)

Job ID: R0241066
Location: Gurugram, Haryana, India
Work Model: Hybrid
Employment Type: Full-Time
Experience Required: Minimum 8 Years in Regulatory Affairs within Medical Device or Healthcare Industry

About the Company

Fresenius Medical Care is a global leader in kidney care, dedicated to improving the lives of patients with chronic kidney disease. With operations across more than 100 countries, the organization delivers innovative medical devices, pharmaceutical products, and digital health solutions that support patient safety and clinical excellence worldwide.

Within its Care Enablement segment, the Systems, Quality & Regulatory (SQR) function ensures regulatory compliance, product quality, post-market surveillance, and lifecycle management across global markets.

Role Overview

The Manager – Regulatory Affairs & Quality Assurance is responsible for overseeing regulatory strategy, compliance management, and quality systems for medical devices and pharmaceutical products across India and the South Asia region.

This leadership role manages product registrations, renewals, change variations, pharmacovigilance responsibilities, regulatory audits, quality management systems, distributor compliance, and post-market surveillance activities. The position requires deep expertise in CDSCO regulations, GMP, GDP, ISO standards, and regulatory intelligence systems.

This opportunity is ideal for senior regulatory professionals seeking leadership roles in medical device registration, pharmaceutical compliance, and quality governance within a global healthcare organization.

Key Responsibilities

Regulatory Strategy & Submissions

  • Lead medical device and drug registrations with CDSCO, State FDA offices, and other health authorities.

  • Execute regulatory submission plans including renewals, variations, and notifications.

  • Liaise with regulatory agencies to resolve compliance issues and negotiate approvals.

  • Maintain and update regulatory dossiers, technical files, and documentation across South Asia markets.

  • Manage Regulatory Information Management Systems (RIMS) and ensure accurate product data governance.

Quality & Compliance Management

  • Implement and maintain Quality Management Systems (QMS) aligned with GMP and GDP requirements.

  • Ensure labeling and redressing compliance in accordance with Good Manufacturing Practices.

  • Oversee MRP implementation and NPPA compliance.

  • Monitor distributor and supplier regulatory compliance.

  • Ensure safe and compliant product release and distribution within GDP frameworks.

Pharmacovigilance & Post-Market Surveillance

  • Fulfill responsibilities as PVRP/Dy PVRP including PSUR submissions, RMP implementation, and PV audits.

  • Manage adverse event and medical device incident reporting in compliance with local regulations.

  • Oversee customer complaint handling and regulatory conformity processes.

  • Support post-market surveillance and corporate drug safety communications.

Audit & Inspection Readiness

  • Ensure preparedness for regulatory inspections and internal audits.

  • Lead corrective and preventive actions (CAPA) for deviations and non-conformities.

Stakeholder & Cross-Functional Collaboration

  • Provide regulatory guidance to Commercial Operations, Supply Chain, Marketing, Legal, and Compliance teams.

  • Participate in monthly Quality and Regulatory Affairs meetings.

  • Support import/export compliance and tender documentation.

  • Maintain transparent communication on regulatory risks and portfolio strategy.

Required Qualifications

  • Bachelor’s Degree in Pharmacy, Chemical Engineering, Bioengineering, or Health Sciences.

  • Minimum 8 years of industry experience in Regulatory Affairs within medical devices or healthcare/pharmaceutical sector.

  • Strong engagement experience with Health Authorities (HAs) in India and South Asia.

  • Comprehensive knowledge of CDSCO regulations, ISO 9001, ISO 13485, GMP, GDP, and regional regulatory laws.

  • Experience leading negotiations and managing medical device registrations.

  • Fluency in English (written and spoken).

  • Advanced proficiency in MS Office and regulatory systems.

Preferred Qualifications

  • Master’s degree in Regulatory Affairs, Quality Management, Pharmaceutical Sciences, or related discipline.

  • Knowledge of ISO 31000 risk management standards.

  • Experience in MedTech regulatory environments.

Core Competencies

  • Regulatory Strategy & Market Access

  • Medical Device & Drug Registration (CDSCO)

  • Pharmacovigilance Leadership (PSUR, RMP, PV Audits)

  • Quality Management Systems (QMS)

  • GMP & GDP Compliance

  • Regulatory Intelligence & Data Governance

  • Audit & Inspection Management

  • Stakeholder Negotiation & Cross-Functional Leadership

Why Join Fresenius Medical Care

  • Opportunity to work with a global leader in kidney care and medical innovation.

  • Exposure to multi-country regulatory environments across South Asia.

  • Strategic leadership role influencing portfolio and compliance decisions.

  • Hybrid work model with international collaboration.

  • Structured career development within a global healthcare enterprise.

Job Category:
Regulatory Affairs – Medical Devices & Pharmaceuticals
Quality Assurance – Healthcare
Pharmacovigilance & Compliance
Healthcare Regulatory Leadership
Medical Device Registration – India

This Manager – Regulatory Affairs & Quality Assurance position is designed for senior regulatory professionals with strong expertise in CDSCO registrations, QMS implementation, pharmacovigilance compliance, and health authority engagement across India and South Asia. It offers a strategic leadership opportunity within a globally recognized healthcare organization.