CMC Specialist: Regulatory Chemistry Lead (Hybrid UK)

Kenvue Inc.; Reading; Hybrid; GBP 60,000 - 90,000; Full time

Job summary

Kenvue Inc. in Reading, UK, is seeking a CMC Specialist to lead lifecycle management and regulatory assessments across the EMEA region and beyond where relevant.

You will provide regulatory input to product development teams within the Self Care franchise and serve as the CMC representative on cross‑functional project teams. You will oversee the authoring and review of CMC documentation, coordinate regional submissions, manage change control, and ensure ongoing compliance for commercial products

Qualifications

• Experience leading CMC regulatory activities, including submissions and post-approval changes.
• Ability to interpret regulatory guidelines and assess impact on technical content.
• Coordinate cross-functional teams to ensure timely regulatory delivery.

Responsibilities

• Lead deployment of CMC regulatory content for Self Care medicinal products.
• Provide technical/regulatory direction for post-approval activities.
• Prepare CMC information for regional agency submissions and compliance.
• Represent CMC in cross-functional project teams and assess regulatory implications.
• Manage daily delivery of regulatory activities and change control.
• Support alignment of processes and simplifications within the team.

Skills

CMC regulatory knowledge

Regulatory submissions

Cross-functional collaboration

Regulatory compliance

Job description

Kenvue Inc. in Reading, UK, is seeking a CMC Specialist to lead lifecycle management and regulatory assessments across the EMEA region and beyond where relevant.

You will provide regulatory input to product development teams within the Self Care franchise and serve as the CMC representative on cross‑functional project teams. You will oversee the authoring and review of CMC documentation, coordinate regional submissions, manage change control, and ensure ongoing compliance for commercial products