Global Regulatory Labeling Lead — Senior Consultant

Parexel; Canada; On-site; CAD 90,000 - 125,000; Full time

Job summary

A global regulatory affairs firm in Canada seeks a Senior Regulatory Affairs Consultant specializing in labeling. You will lead complex global labeling initiatives, ensuring compliance with international regulations and overseeing product lifecycle management. The ideal candidate has 5-7 years' experience in the biotech/pharmaceutical sector and strong collaborative skills within cross-functional teams. Join us to make a worldwide impact in regulatory affairs and contribute to incisive governance processes.

Qualifications

• University degree in Life Sciences or related Pharmaceutical field.
• Advanced degree (MSc, PhD, PharmD) preferred.
• Minimum of 5-7 years in the biotech/pharmaceutical industry.
• At least 2 years of labeling/regulatory experience with global responsibilities.

Responsibilities

• Lead and coordinate labeling activities across markets.
• Ensure compliance with global regulatory requirements.
• Manage GRA label compliance processes and oversight.
• Prepare documents for Labeling Review Committee meetings.
• Review and approve marketing advertising and medical education content.

Skills

Global Regulatory Labeling Management

Collaboration

Regulatory Knowledge

Attention to Detail

Communication Skills

Education

University degree in Life Sciences

Advanced degree (MSc, PhD, PharmD) preferred

Tools

Veeva RIMS

Microsoft Office

Adobe Acrobat

Job description

A global regulatory affairs firm in Canada seeks a Senior Regulatory Affairs Consultant specializing in labeling. You will lead complex global labeling initiatives, ensuring compliance with international regulations and overseeing product lifecycle management. The ideal candidate has 5-7 years' experience in the biotech/pharmaceutical sector and strong collaborative skills within cross-functional teams. Join us to make a worldwide impact in regulatory affairs and contribute to incisive governance processes.