Global Regulatory Affairs Specialist

Tecnimede Group; Sintra; On-site; EUR 35,000 - 55,000; Full time

Job summary

A multinational pharmaceutical company is seeking a Regulatory Affairs Specialist to ensure compliance with regulations and prepare product registration dossiers. The ideal candidate should have a background in Pharmacy or Chemistry and proven experience in the pharmaceutical regulatory field. Strong communication skills and fluency in English are essential. This role offers a unique opportunity to make a significant impact within a dynamic team in Lisbon.

Qualifications

• Proven experience in the pharmaceutical regulatory area.
• In-depth knowledge of pharmaceutical legislation and regulations.

Responsibilities

• Ensure compliance with applicable regulations and guidelines.
• Prepare and submit pharmaceutical product registration dossiers.
• Keep regulations updated and ensure company compliance.
• Collaborate with internal teams during pre-authorization and post-authorization.

Skills

Analytical skills

Problem-solving skills

Excellent verbal communication

Excellent written communication

Ability to work independently

Ability to work in a team

Fluency in English

Education

Academic training in Pharmacy, Chemistry or related field

Job description

A multinational pharmaceutical company is seeking a Regulatory Affairs Specialist to ensure compliance with regulations and prepare product registration dossiers. The ideal candidate should have a background in Pharmacy or Chemistry and proven experience in the pharmaceutical regulatory field. Strong communication skills and fluency in English are essential. This role offers a unique opportunity to make a significant impact within a dynamic team in Lisbon.