Junior Regulatory Affairs Consultant Hybrid, Global Growth

regenold GmbH; Portugal; Hybrid; EUR 26,000 - 40,000; Full time

Job summary

regenold Portugal is seeking a Junior Regulatory Affairs Consultant to join our international Regulatory Affairs team and grow your career within regenold. You will support European regulatory projects, contribute to documentation and strategies, and work closely with teams across regenold in Germany, the UK, Ireland and Portugal.

You will gradually take on increasing responsibility, gain exposure to international clients and regulatory activities across the product lifecycle, and may contribute

Qualifications

• Up to 2 years of professional experience in Regulatory Affairs; internships or academic projects valued.
• Basic knowledge of European regulatory procedures and the medicinal product lifecycle.
• Motivation to learn, take responsibility and develop within a consulting environment.
• Very good written and spoken English; additional European languages are an advantage.

Responsibilities

• Support national, decentralised, mutual recognition and centralised regulatory procedures throughout the product lifecycle.
• Prepare, compile and review regulatory documentation for submissions in Portugal and across Europe.
• Collaborate closely with experts in Quality, Pharmacovigilance, CMC, Medical Devices and Market Access to support integrated regulatory solutions.
• Monitor regulatory developments and help assess their practical impact on clients and projects.
• Maintain accurate project records, trackers and regulatory databases, ensuring deadlines and commitments are followed.

Skills

EU regulatory knowledge

Cross-functional collaboration

Regulatory operations

Project management

Education

University degree in Pharmacy/Pharmaceutical Sciences

Job description

regenold Portugal is seeking a Junior Regulatory Affairs Consultant to join our international Regulatory Affairs team and grow your career within regenold. You will support European regulatory projects, contribute to documentation and strategies, and work closely with teams across regenold in Germany, the UK, Ireland and Portugal.

You will gradually take on increasing responsibility, gain exposure to international clients and regulatory activities across the product lifecycle, and may contribute