Hybrid Regulatory Affairs Lead for Global Lifecycle

Orion Pharma; Espoo; Hybrid; EUR 95,000 - 130,000; Full time

Benefits offered by this job

Hybrid work model

Job summary

Orion Pharma is seeking a Regulatory Affairs Lead based in Espoo or Turku, Finland, to shape regulatory strategies and steer activities across a diverse product portfolio. You will report to the Head of Global Regulatory Affairs, LCM, and collaborate with internal teams, external partners and authorities in a global context.

The role requires about 10 years in regulatory affairs for pharmaceutical products, a strong grasp of European guidelines, and excellent communication skills in English;

Qualifications

• Approximately 10 years of regulatory affairs experience in pharma products.
• Strong knowledge of European pharmaceutical legislation and procedures.
• Excellent communication and teamwork in an international setting.
• Fluent English; Finnish language skills are a strong advantage.

Responsibilities

• Regulatory Intelligence to inform product lifecycle management.
• Provide regulatory guidance to cross‑functional teams.
• Develop and improve regulatory processes to ensure GxP compliance.
• Coordinate interactions with regulatory authorities and partners.

Skills

Regulatory expertise

Cross-functional collaboration

English proficiency

Finnish language

Leadership

Education

M.Sc. in Pharmacy

Job description

Orion Pharma is seeking a Regulatory Affairs Lead based in Espoo or Turku, Finland, to shape regulatory strategies and steer activities across a diverse product portfolio. You will report to the Head of Global Regulatory Affairs, LCM, and collaborate with internal teams, external partners and authorities in a global context.

The role requires about 10 years in regulatory affairs for pharmaceutical products, a strong grasp of European guidelines, and excellent communication skills in English;