Regulatory Affairs PLM Associate: Lifecycle & Submissions

Haleon plc.; Weybridge; On-site; GBP 35,000 - 55,000; Full time

Job summary

Haleon plc, a leading consumer health company, seeks a Regulatory Affairs professional to manage lifecycle maintenance and renewal activities across brands. You will coordinate with Safety, CMC, Manufacturing, and operating units to ensure timely regulatory submissions and high-quality documentation.

With 1–3+ years of experience and a strong science background, you will contribute to global regulatory strategies, support regional expansion, and help ensure compliant product dossiers in a

Qualifications

• Basic understanding of Regulatory Affairs and product lifecycles.
• 1–3+ years of relevant experience.
• Strong scientific background in Pharmaceutical or Life Sciences.

Responsibilities

• Maintain understanding of global regulatory requirements for lifecycle maintenance and renewal activities.
• Agree and communicate regulatory submission plans with markets to meet timelines.
• Prepare high‑quality documents for renewal and safety reporting using market data requirements.
• Provide Centre of Excellence support to Operating Units for regional initiatives and new product introductions.
• Act as regulatory expert within project teams and drive regulatory strategy across functions.

Skills

Regulatory knowledge

Communication

Team collaboration

Education

BSc or related degree

Tools

Veeva Vault

Job description

Haleon plc, a leading consumer health company, seeks a Regulatory Affairs professional to manage lifecycle maintenance and renewal activities across brands. You will coordinate with Safety, CMC, Manufacturing, and operating units to ensure timely regulatory submissions and high-quality documentation.

With 1–3+ years of experience and a strong science background, you will contribute to global regulatory strategies, support regional expansion, and help ensure compliant product dossiers in a