Regulatory Strategy Lead – Cosmetics & Devices | Hybrid

Perrigo; Greater London; Hybrid; GBP 55,000 - 75,000; Full time

Benefits offered by this job

Hybrid work model

Forbes recognition

Total Rewards program

Job summary

Perrigo is seeking a Regulatory Affairs professional to support cosmetic, medical device and medicines products across global markets. The role focuses on regulatory strategy, documentation, and submissions, with emphasis on new product development and geo-expansion.

The successful candidate will join a hybrid work environment, collaborate across teams, and contribute to ensuring compliance for consumer healthcare brands. Fluency in English is required.

Qualifications

• Bachelor’s Degree in Life Sciences.
• Minimum 3 years in Regulatory Affairs.
• Expertise in Cosmetic Product Regulation and regulatory affairs for medical device or medicines products in consumer healthcare or self-care in EU, US or other markets.
• Fluent in English.

Responsibilities

• Provide regulatory input to new product development, geo-expansion and existing product innovation for assigned product portfolio.
• Contribute to regulatory strategy development for innovation projects for all markets in scope (gathering and drafting requirements, identifying pathways to market and supportable claims).
• Prepare technical documentation components for submissions, PIFs and labelling in line with document management processes.
• Support master label and artwork development and claims review.
• Support registration/notification procedures for certification of new products and may communicate with Notified Bodies and regulatory authorities as needed.
• Responsible for managing central Cosmetic Product Notifications.
• Support due diligence activities and gap analysis assessments.
• Support smooth handover/transition to LCM following initial launch.
• Build regulatory knowledge via regulatory intelligence, training and networking.

Skills

Regulatory Affairs

Education

Bachelor’s Degree in Life Sciences

Job description

Perrigo is seeking a Regulatory Affairs professional to support cosmetic, medical device and medicines products across global markets. The role focuses on regulatory strategy, documentation, and submissions, with emphasis on new product development and geo-expansion.

The successful candidate will join a hybrid work environment, collaborate across teams, and contribute to ensuring compliance for consumer healthcare brands. Fluency in English is required.