Vice President, Global Head of Regulatory Affairs

Azurity Pharmaceuticals - India

$150K — $200K *
Pharmaceuticals & Biotech
11 - 15 years of experience
Job Overview by Ladders

Qualifications

  • MD, PhD, or PharmD preferred with 15+ years in Regulatory Affairs
  • Proven success in global regulatory submissions and approvals
  • Deep expertise across FDA, EMA, and international regulatory frameworks
  • Strong NCE and clinical development experience
  • Experience leading major health authority interactions (e.g., pre-NDA/BLA, EOP2)
  • Strong leadership experience managing global regulatory teams
  • Expertise in GxP and global compliance requirements

Responsibilities

  • Lead global regulatory strategy across multiple complex programs
  • Oversee regional regulatory teams to ensure compliant submissions
  • Direct global submissions and approvals while managing risks
  • Lead interactions and negotiations with FDA, EMA, and global regulators
  • Partner cross-functionally to align regulatory and market access strategies
  • Monitor regulatory trends and adapt development strategies
  • Build and lead a high-performing global RA organization

Benefits

  • Unlock your earning potential with a competitive compensation package and performance-based bonuses
  • Comprehensive health coverage including medical, dental, vision, and prescription plans
  • Flexible hybrid work model, allowing for work-life balance
  • Retirement savings plan with matching contributions up to 5%
  • Generous time off policy with up to 15 vacation days and holiday closures
  • Tuition reimbursement for further education and professional development
  • Peer recognition platform to celebrate contributions and achievements
Full Job Description
Overview

We are seeking a strategic and influential VP, Global Head of Regulatory Affairs to lead global regulatory strategy and execution across a diverse and complex portfolio. This role drives regulatory success from development through post-approval, ensuring timely submissions, approvals, and global compliance.

Key Responsibilities
  • Lead global regulatory strategy across multiple complex programs
  • Oversee regional regulatory teams and ensure high-quality compliant submissions
  • Direct global submissions and approvals while managing risks
  • Lead interactions and negotiations with FDA, EMA, and global regulators
  • Partner cross-functionally to align regulatory and market access strategies
  • Monitor regulatory trends and adapt development strategies
  • Ensure global compliance and oversee vendors/CROs
  • Build and lead a high-performing global RA organization
  • Communicate risks and strategic insights to leadership

Qualifications
  • MD, PhD, or PharmD preferred with 15+ years in Regulatory Affairs
  • Proven success in global regulatory submissions and approvals
  • Deep expertise across FDA, EMA, and international regulatory frameworks
  • Strong NCE and clinical development experience
  • Experience with 505(b)(2) and/or EU Hybrid pathways preferred
  • Experience leading major health authority interactions (e.g., pre-NDA/BLA, EOP2)
  • Strong leadership experience managing global regulatory teams
  • Expertise in GxP and global compliance requirements
  • Strategic thinker with strong problem-solving and execution skills
  • Excellent communication and stakeholder management skills
  • Experience in fast-paced or entrepreneurial environments is a plus

#LI-Hybrid

Physical & Mental Requirements:

The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
  • Must be able to sit for long periods of time
  • While performing the duties of this job, the employee is frequently required to stand; walk; sit; talk and/or hear
  • May occasionally climb stairs and/or ride elevators
  • The employee must occasionally lift and/or move up to 25 pounds
  • Employee must be able to manipulate keyboard, operate a telephone and hand-held devices
  • Other miscellaneous job duties as required

Benefits We Offer:
  • Unlock Your Earning Potential: Join our team and be rewarded with a competitive compensation package, including an annual bonus based on company performance, that recognizes your exceptional talent.
    • Sales - In lieu of annual bonuses, we offer an Incentive compensation program that allows you to earn more - even over plan.
    • Fuel Your Success: *Sales Only* - We understand the value of your hard work and provide a car reimbursement program and gas card for both business and personal use as part of our commitment to supporting you.
  • Comprehensive Health Coverage: We value your well-being and offer excellent medical, dental, vision, and prescription coverage to ensure you and your family are always taken care of.
  • Flexibility for Your Lifestyle: Achieve work-life balance with our hybrid work model, allowing you to work two days from home and three days in the office. *Excludes Sales, Manufacturing, and some Operations positions*
  • Invest in Your Future: Our Retirement Savings Plan (401K) is designed to help you secure a comfortable retirement by matching dollar for dollar up to 5%.
  • Time Off That Counts: Take advantage of our generous time off policy, which offers up to 15 vacation days annually + rollover (up to 40 hours) as well as five sick/wellness days. For new employees, vacation accrual will be prorated based on your start date.
  • Meaningful Time with Your Loved Ones: We close between Christmas and New Year's to give you an extra week off to spend quality time with your family and recharge.
  • Enjoy the Holidays: Over the course of the year, Azurity recognizes 13 holidays.
  • Invest in Your Education: We support your professional growth with tuition reimbursement for undergraduate and graduate level courses or certifications.
  • Recognize and Be Recognized: Our Azurity High Five peer recognition platform allows you to celebrate your colleagues' accomplishments and receive recognition for your own outstanding work.

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