Regulatory Affairs Associate, Global - Hybrid

Aurora Cannabis Inc.; Ontario; Hybrid; CAD 60,000 - 100,000; Full time

Job summary

An innovative global cannabis company is seeking a Regulatory Affairs Associate to provide essential regulatory support for international exports. This role is pivotal in ensuring compliance with regional regulations and involves collaboration with cross-functional teams. The ideal candidate will have a strong background in regulatory affairs, particularly in biopharmaceuticals, and will thrive in a dynamic environment. Join a diverse and inclusive team that values flexibility and rewards innovation, where your contributions will directly impact the success of the organization.

Benefits

Flexible Hours

Remote Options

Competitive Salary

Development Opportunities

Team Activities

Modern Tech

Qualifications

• 5+ years of regulatory experience in biopharmaceuticals or health authorities.
• Strong project management skills and ability to interpret regulations.

Responsibilities

• Ensure compliance and successful regulatory strategies for international exports.
• Build relationships with experts to support regulatory strategies.

Skills

Regulatory Compliance

Project Management

Communication Skills

Strategic Thinking

Education

University Degree in Science

Job description

Regulatory Affairs Associate, Global - Hybrid

Join us at Aurora Cannabis Inc. as a Regulatory Affairs Associate, Global - Hybrid.

Division: Legal
Location: Hybrid (Ontario)
Hours: 40 hours/week, Monday to Friday
Employment: Temporary (12-Month Contract)

About Us

Hi, we’re Aurora Cannabis, a global cannabis company operating across Europe, North and South America. We are passionate about improving lives through our innovative brands like Aurora, Aurora Drift, San Rafael ’71, Greybeard, and Whistler. Our diverse team, the "A-Team," is committed to excellence and bold innovation to deliver the best cannabis experience.

Job Summary

The Regulatory Affairs Associate, Global provides regulatory support for Aurora’s international exports from Canadian facilities. This role involves collaboration with cross-functional teams to ensure compliance and successful regulatory strategies across regions.

Key Responsibilities

1. Understanding regulatory frameworks and regional trends for applications and licensing.
2. Building relationships with internal and external experts to support regulatory strategies and exports.
3. Sharing best practices in handling applications and procedures with health authorities.
4. Contributing to submission planning, preparation, and delivery throughout product lifecycle.
5. Supporting project planning, resource management, and risk escalation.
6. Maintaining compliance activities, submission tracking, and document management.
7. Developing process improvements.
8. Engaging with international regulators and business units.
9. Performing other duties as assigned.

Qualifications

• University Degree in Science or related discipline.
• Minimum 5 years of regulatory experience in biopharmaceuticals, health authorities, or relevant fields.
• Strong project management skills.
• Ability to interpret regulations within scientific and commercial contexts.
• Experience in regulated environments like GMP, consumer goods, or pharmaceuticals.

Preferred Skills

• Knowledge of cannabis, GMP, and related products with Health Canada.
• Strong collaboration, communication, and strategic thinking skills.
• Ability to work independently with multiple deadlines and adapt to changing priorities.

Why Join Aurora?

• Flexibility: Flexible hours, remote options, and more.
• Rewards: Competitive salary, development opportunities, team activities, and modern tech.
• Team: A diverse, inclusive, and passionate global team.

Next Steps

Apply via our website. We review applications promptly and contact suitable candidates. Don’t meet all requirements? Apply anyway or share with your network. Aurora values diversity and inclusion, and we accommodate applicants during the recruitment process.