Job Description: DGM – Regulatory (Medical Devices)
Company Details
Company: Sun Pharmaceutical Industries Ltd
Business Unit: GDO
Job Grade: G8
Work Locations: Gurgaon / Mumbai, India
Function: R&D – Regulatory Affairs
Date Posted: May 19, 2026
Job Title
Deputy General Manager (DGM) – Regulatory Affairs (Medical Devices)
Role Overview
The DGM – Regulatory (Devices) is responsible for defining and executing global regulatory strategies for medical devices, including combination products and companion diagnostics. The role ensures successful regulatory submissions, approvals, and lifecycle management across major regulated markets, including the United States, European Union, and Canada.
The position requires strong leadership in global regulatory strategy, cross-functional collaboration, and engagement with health authorities.
Key Responsibilities
1. Global Regulatory Strategy
Develop and maintain end-to-end regulatory strategies for medical devices
Align regulatory plans with product design, intended use, risk classification, and business goals
Define regulatory pathways for US, EU, and Canada markets
2. Regulatory Submissions & Approvals
Prepare, review, and manage regulatory submissions including:
FDA 510(k), PMA, IDE, HDE
EU MDR / CE marking dossiers
Health Canada device licensing applications
Ensure accuracy, consistency, and compliance of submissions
Manage responses to regulatory authority queries and deficiencies
3. Lifecycle Management (LCM)
Manage post-approval changes and regulatory maintenance activities
Lead change impact assessments for:
Design modifications
Manufacturing and process changes
Supplier/raw material changes
Labeling updates
Submit change notifications and maintain regulatory dossiers (including annual reports)
4. Technical & Clinical Regulatory Support
Provide regulatory input on:
Human factors and usability engineering
Design and development documentation
Verification and validation activities
Evaluate preclinical data (bench testing, biocompatibility, electrical safety, EMC, etc.)
Assess clinical data to ensure alignment with regulatory requirements and product claims
5. Agency Interaction & Communication
Serve as primary regulatory contact for health authorities
Manage regulatory correspondence and deficiency responses
Lead pre-submission meetings and regulatory strategy discussions with agencies
Incorporate agency feedback into development and submission plans
6. Cross-Functional Leadership
Act as regulatory lead in cross-functional project teams
Translate regulatory requirements into actionable development plans
Collaborate with R&D, quality, clinical, and manufacturing teams
Ensure compliance with ISO standards and global regulations
7. Quality & Compliance Oversight
Oversee:
Supplier qualification
CAPA management
Complaint handling
Product performance monitoring
Regulatory audits
8. Regulatory Intelligence
Monitor global regulatory updates and evolving guidelines
Assess impact of regulatory changes on product development and approvals
Recommend strategies for compliance and market access
Qualifications
Educational Background
Bachelor’s degree in:
Life Sciences
Engineering
Biomedical Sciences
Or related field
Master’s degree preferred (PhD / MBA advantageous)
Experience Requirements
15+ years of progressive experience in medical device regulatory affairs
Strong hands-on experience with:
FDA submissions (510(k), PMA, IDE)
EU MDR / CE marking
Health Canada regulatory processes
Experience in combination products (drug-device) is mandatory
Skills & Competencies
Technical Expertise
Global regulatory strategy development
Regulatory dossier authoring and submission
ISO standards and regulatory compliance
Audit and inspection readiness
Complaint and CAPA management
Leadership & Organizational Skills
Experience building and leading teams
Strong coaching and mentoring capabilities
Resource planning and workload prioritization
Cross-functional leadership in global environments
Communication & Strategic Skills
Strong written and verbal communication
Ability to engage with global regulatory agencies
Stakeholder management across regions
Strategic thinking and decision-making
Travel Requirement
Travel may be required based on business needs
Uttar Pradesh :
Agra | Gajraula | Gautam buddha Nagar | Ghaziabad | Gorakhpur | Greater Noida | Jhansi | kanpur | Lucknow | Mathura | Noida | Park City | Prayagraj | Satyamev | Varanasi |Gujarat :
Ahmedabad | Ankleshwar | Baroda | Bharuch | Gandhinagar | Gujarat | Halol | Jhagadia | Mehsana | surat | Tarasadi | Vadodara | Vapi |Maharashtra :
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Hajipur | Patna |Kerala :
Kannur | Kochi | Malappuram | Thiruvananthapuram | Trivandrum |Pondicherry (Puducherry) :
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Rangpo |India :
Remote, India | Siliguri |Illinois :
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Frank Scottile Blvd |Missouri :
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Berlin |Baden-Wurttemberg :
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Frankfurt | Harveysburg |Germany :
Germany | GErmany |Lower Saxony :
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Europe | France | Latvia | Lendava | Leuven | Poland | Slovenia | Spain |Finland :
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Istanbul | Turkey |Norway :
Norway | NOrway |Romania :
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Dún Laoghaire |Galway :
Galway |County Dublin :
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Beijing |China :
China | Quarry Bay |Liaoning :
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Hangzhou |Tokiyo :
Osaka | Tokyo |Shanghai Sai :
Shanghai Shi |Hubei :
Wuhan |Capital of Netherland :
Amsterdam |North Brabant :
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Haarlem |South Holland :
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Netherlands |Remote Australia :
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Queensland |Melbourne :
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England | Harlow | Leeds | London | Maidenhead | Salt Lake City | Stevenage | Stirling | United Kingdom |North Yorkshire :
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Canada |Quebec :
Montreal |Brussels :
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Auckland |New Zealand :
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Cebu City |Philippines :
Manila |Croatia :
Croatia |Zagreb :
Zagreb |Estonia :
Tartu | Estonia |Harju County (Maakond) :
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Ho Chi Minh City |Italy :
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Jakarta |East Java :
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Japan | Saitama |Tokyo :
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Singapore |Sofia City :
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Sweden |Taipei :
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Warsaw |