Haleon is a global leader in consumer health, dedicated to improving everyday health for billions of people. With a powerful portfolio of trusted brands like Sensodyne, Panadol, Advil, Voltaren, Theraflu, Otrivin, and Centrum, Haleon combines deep human understanding with trusted science to deliver innovative healthcare solutions.
At Haleon, we foster an inclusive and agile work environment where employees can grow, innovate, and shape the future of consumer health. Join us in making a meaningful impact on global healthcare.
Job Description
Job Purpose:
The Regulatory Affairs CMC Associate will execute Chemistry, Manufacturing, and Controls (CMC) regulatory activities for new product registrations and lifecycle management (including variations and renewals) for an assigned product portfolio.
Key Responsibilities:
- Prepare CMC sections for new product registrations, variations, renewals, and responses to regulatory agency queries.
- Collaborate with global teams (Category, BU, Quality, Supply Chain) to ensure high-quality CMC dossiers and compliance with business priorities.
- Maintain up-to-date technical product records and ensure regulatory compliance.
- Evaluate potential CMC changes and ensure proper documentation (e.g., change controls).
- Support regulatory submissions for clinical trials (INDs/CTAs) and other regulatory filings.
Preferred Skills & Qualifications:
- Degree in Pharmaceutical Sciences, Life Sciences, or related field (or equivalent regulatory experience).
- 3-5 years of experience in Regulatory Affairs (CMC focus).
- Knowledge of Quality, Manufacturing, Product Development, and OTC regulations.
- Experience in regulatory information management systems (RIMS) and compliance.
- Strong communication and collaboration skills.
Why Join Haleon?
- Work with world-renowned consumer health brands.
- Be part of an inclusive and diverse workplace.
- Opportunities for professional growth and innovation.
- Flexible work culture that supports work-life balance.
How to Apply
