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Dgm - Regulatory Expert Medical Device

Sun Pharma
15+ years
$250,000 – $350,000
Gurgaon, Mumbai, India
10 June 16, 2026
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Clinical Trials, Detail-Oriented, Drug Development, Lifesciences, Negotiation Skills, Regulatory Compliance, Communication Skills, CPC Certified, Data Analysis, Document Management, Life Science, Regulatory Compliance, Waterfall Model, 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

Key Responsibilities

1. Regulatory Strategy & Planning

  • Develop and maintain end-to-end regulatory strategies for medical devices.

  • Align regulatory pathways with:

    • Product technology

    • Intended use

    • Risk classification

    • Business objectives

  • Lead global regulatory planning for major submissions and approvals.


2. Regulatory Submissions

Prepare, review, and manage submissions including:

  • FDA 510(k)

  • PMA (Premarket Approval)

  • IDE (Investigational Device Exemption)

  • HDE (Humanitarian Device Exemption)

  • Health Canada Medical Device Licenses

  • EU MDR CE Marking submissions

Ensure all submissions are accurate, compliant, and delivered on time.


3. Lifecycle Management (LCM)

  • Manage annual reports and post-approval submissions.

  • Conduct change impact assessments for:

    • Design modifications

    • Manufacturing changes

    • Process changes

    • Supplier changes

    • Raw material changes

    • Labeling updates

  • Determine reporting requirements and manage regulatory notifications.


4. Design & Development Support

Provide regulatory guidance for:

  • Human Factors Engineering

  • Usability Engineering

  • Design Controls

  • Verification & Validation Activities

  • Risk Management Documentation


5. Clinical & Preclinical Review

Review and assess:

  • Bench Testing

  • Biocompatibility Studies

  • Electrical Safety Testing

  • EMC Testing

  • Clinical Investigation Data

  • Performance Evidence

Ensure data supports intended use, claims, and regulatory requirements.


6. Quality & Compliance Oversight

Lead activities related to:

  • Supplier Qualification

  • CAPA Management

  • Complaint Handling

  • Product Performance Monitoring

  • Internal & External Audits


7. Regulatory Agency Interactions

Serve as primary contact for:

  • FDA

  • Health Canada

  • European Regulatory Authorities

  • Notified Bodies

Responsibilities include:

  • Deficiency responses

  • Regulatory meetings

  • Pre-submissions

  • Agency communications

  • Approval negotiations


8. Cross-Functional Leadership

  • Act as Regulatory Lead on project teams.

  • Translate complex regulatory requirements into executable plans.

  • Collaborate with:

    • Clinical

    • Quality

    • Manufacturing

    • R&D

    • Commercial teams


9. Regulatory Intelligence

  • Monitor evolving regulations and guidance.

  • Assess regulatory impact on products and development programs.

  • Recommend optimal approval pathways.


Educational Qualifications

Required

  • Bachelor's Degree in:

    • Life Sciences

    • Biomedical Sciences

    • Engineering

    • Related Scientific Discipline

Preferred

  • Master's Degree

  • MBA

  • PhD


Experience Required

Total Experience

  • 15+ years of progressive Medical Device Regulatory Affairs experience

Mandatory Expertise

  • FDA 510(k)

  • PMA

  • IDE

  • EU MDR

  • CE Marking

  • Health Canada Device Licensing

  • Combination Products (Drug-Device)


Key Skills & Competencies

Regulatory Expertise

  • Global regulatory strategy

  • Medical device registrations

  • Health authority interactions

  • Product labeling

  • Regulatory documentation


Quality & Compliance

  • ISO Standards

  • Audit Management

  • Complaint Management

  • CAPA

  • Supplier Quality


Leadership

  • Team building

  • Coaching & mentoring

  • Resource allocation

  • Workload prioritization

  • Stakeholder management


Communication

  • Strong written communication

  • Strong verbal communication

  • Regulatory negotiation skills

  • Executive-level presentations


Travel Requirement

  • Moderate travel expected based on regulatory meetings, audits, inspections, and global stakeholder interactions.