Director, Regulatory Affairs

Allucent; India; Hybrid; INR 3,000,000 - 6,000,000; Full time

Benefits offered by this job

Comprehensive benefits package per loc

Competitive salaries per location

Training budget for professional dev

Flexible working hours

Remote/hybrid depending on location

Leadership and mentoring opportunities

Employee referral program

Job summary

Allucent in India is seeking a Director of Regulatory Affairs to guide clients through drug, biologic, and medical device development. You will lead regulatory teams, shape strategies, and ensure timely, high-quality submissions.

As a trusted expert in HA interactions, you will translate regulatory requirements into actionable plans and mentor project teams across diverse initiatives. This role offers flexible hybrid working and opportunities to advance global healthcare.

Qualifications

• Requires scientific degree (B.Sc., M.Sc., Ph.D. or equivalent) in a scientific area and experience in drug, biologic, or device development.
• 8 years' experience with regulatory requirements of US FDA, Health Canada and/or European authorities.
• Advanced regulatory knowledge for US, EU, and Canada.

Responsibilities

• Has advanced knowledge of Health Authority (HA) Regulatory Guidance & Regulations for regulatory filings through all phases of development and lifecycle management.
• Reviews and prepares HA meeting requests and briefing documents.
• Oversees and manages regulatory projects of varying complexities.
• Provides strategic advice and expertise in translating regulatory requirements into practical plans and solutions.
• Has advanced knowledge of CTD format and structure for regulatory submissions.

Education

B.Sc., M.Sc., Ph.D. or equivalent degree in science

Job description

Step into a leadership role where your expertise drives innovation. As a Director, Regulatory Affairs, you'll guide clients through the complexities of drug, biologic, and medical device development. Leading teams, shaping strategies, and ensuring successful submissions. This is your chance to be the trusted expert who turns regulations into real-world impact on global healthcare.

About the Role

As a Director of Regulatory Affairs, you will guide clients through the complexities of drug, biologic, and medical device development. You will lead and mentor regulatory teams, shape strategies, and ensure the delivery of high-quality, scientifically sound submissions. You will serve as a trusted expert in Health Authority (HA) interactions and translate regulatory requirements into clear, actionable plans. In this role, you will act as a Subject Matter Expert, Technical Lead, or Consulting Lead across diverse project teams. You will also review and author regulatory and scientific documents while driving successful outcomes for clients. Most importantly, you will make a direct impact on advancing innovative therapies and global healthcare.

Your main responsibilities will include but not limited to:

• Has advanced knowledge of HA Regulatory Guidance & Regulations pertaining to preparation of regulatory filings through all phases of drug or device development and lifecycle management
• Reviews and prepares HA meeting requests and briefing documents.
• Oversees and manages regulatory projects of varying complexities.
• Provides strategic advice and expertise in translating regulatory requirements into practical plans and solutions.
• Has advanced knowledge of CTD format and structure for regulatory submissions.

About You

If you are a strategic leader with deep regulatory expertise across both pre-and-post marketing stages of development and thrive on leading regulatory projects, solving complex regulatory challenges, and making a tangible impact on global healthcare, you'll thrive here.

To be successful we are looking for the following traits and behaviors:

• Requires a B.Sc., M.Sc., Ph.D., or equivalent degree, in a scientific area, and equivalent combination of relevant experience in drug, biologic, or device development
• 8 years' experience with regulatory requirements of US FDA, Health Canada and / or European authorities
• Advanced regulatoryknowledge of drug, biologic, or device development focusing on regulatory requirements for US, EU, and / or Canada

About Allucent

Our mission is to help bring new therapies to light. When you work at Allucent, that means rolling up your sleeves and applying your unique skill set, expertise, and knowledge to build partnerships with our clients in their pursuit to develop new, life-improving treatments.

If you're passionate about helping customers develop new pharmaceuticals and biologics; have an entrepreneurial spirit; and ready to join other science, business, and operations leaders, we would love to get to learn more about how we can help each other grow.

Together we SHINE. Find more information about our values.

Benefits of working at Allucent include:

• Comprehensive benefits package per location
• Competitive salaries per location
• Departmental Study/Training Budget for furthering professional development
• Flexible Working hours (within reason)
• Opportunity for remote/hybrid* working depending on location
• Leadership and mentoring opportunities
• Participation in our enriching Buddy Program as a new or existing employee
• Internal growth opportunities and career progression
• Financially rewarding internal employee referral program
• Access to online soft-skills and technical training via internal platforms
• Eligibility for our Spot Bonus Award Program in recognition of going above and beyond on projects
• Eligibility for our Loyalty Award Program in recognition of loyalty and commitment of longstanding employees