Junior Regulatory Affairs Advisor – Life Sciences

About the role

PwC’s Life Sciences practice is seeking a Junior Regulatory Affairs Advisor to support clients navigating the evolving regulatory landscape across Europe and beyond. You will work alongside experienced consultants to develop regulatory strategies, prepare submissions, and interpret guidance from EMA, FDA and national authorities.

Key responsibilities

• Assist clients in understanding and complying with global regulatory requirements.
• Support the preparation of regulatory submissions and health authority interactions.
• Contribute to the design and improvement of regulatory affairs processes and operating models.
• Analyse new regulatory developments and translate them into actionable recommendations.
• Collaborate with multidisciplinary teams on projects covering market access, commercialization and patient engagement.

Required profile

• 1–2 years of regulatory affairs experience in the pharmaceutical, biotechnology or broader life‑sciences sector.
• Practical exposure to EU pharmaceutical regulations, EMA procedures and/or national competent authorities.
• Experience with regulatory submissions and product lifecycle management.

Required skills

• Knowledge of EMA, FDA and national regulatory frameworks.
• Familiarity with regulatory information management (RIM) concepts.

What we offer

• Opportunities to work on high‑impact projects for leading life‑sciences companies.
• Professional development within a global advisory firm.
• Collaborative environment that encourages learning and innovation.