Global Regulatory Strategist — Cosmetics & MedTech

Perrigo Company plc; Lisboa; Híbrido; EUR 42 000 - 64 000; Tempo integral

Resumo da oferta

Perrigo Company plc in Portugal is seeking a Regulatory Affairs professional to support Cosmetic products and Medical Devices/Medicines regulatory activities across global markets. You will contribute to strategy, prepare technical documentation, manage Cosmetic Product Notifications, and liaise with Notified Bodies and authorities.

The role requires a life sciences degree, 3+ years in regulatory affairs, and fluency in English.

Qualificações

• Bachelor’s Degree in Life Sciences or relevant scientific/technical discipline.
• Minimum 3 years in Regulatory Affairs – position dependant on experience.
• Expertise in Cosmetic Product Regulation and regulatory affairs for medical device or medicines products within consumer healthcare or self-care in EU, US or other markets.
• Fluent in English.

Responsabilidades

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

Conhecimentos

Regulatory Affairs

Cosmetic Regulation

Regulatory Strategy

English Fluency

Formação académica

Bachelor’s Degree in Life Sciences

Descrição da oferta de emprego

Perrigo Company plc in Portugal is seeking a Regulatory Affairs professional to support Cosmetic products and Medical Devices/Medicines regulatory activities across global markets. You will contribute to strategy, prepare technical documentation, manage Cosmetic Product Notifications, and liaise with Notified Bodies and authorities.

The role requires a life sciences degree, 3+ years in regulatory affairs, and fluency in English.