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AstraZeneca

Associate Regulatory Affairs Director

Mississauga, ON, Canada
Canada - Mississauga, Canada

Full-time

Apply About employer

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Job details

Job type: Full-time
Apply by: Oct 16, 2026
Experience: Extensive regulatory experience (5+ years) within the biopharmaceutical industry, or experience at a health authority
Posting language: English
Posted: Oct 8, 2026

Original job description

At AstraZeneca, we pride ourselves on crafting a collaborative culture that champions knowledge-sharing, ambitious thinking and innovation – ultimately providing employees with the opportunity to work across teams, functions and even the globe.

Recognizing the importance of individualized flexibility, our ways of working allow employees to balance personal and work commitments while ensuring we continue to create a strong culture of collaboration and teamwork by engaging face-to-face in our offices 3 days a week. Our head office and in downtown Toronto are purposely designed with collaboration in mind, providing space where teams can come together to strategize, brainstorm and connect on key projects.

Our dedication to sustainability is also central to our culture and part of what makes AstraZeneca a great place to work. We know the health of people, the planet and our business are interconnected which is why we’re taking ambitious action to tackle some of the biggest challenges of our time, from climate change to access to healthcare and disease prevent

The Associate Regulatory Affairs Director (ARAD) is an experienced regulatory specialist with strong project management capabilities responsible for leading the end-to-end planning, coordination, and execution of assigned deliverables. The ARAD is a key contributor to regulatory submission strategy, identifying submission risks and opportunities, while leading complex regulatory applications and managing procedures through approval. The ARAD provides regulatory expertise and guidance on procedural and documentation requirements to cross-functional teams working flexibly within and across regions on different phases of drug development to ensure the delivery of business objectives.

Accountabilities/Responsibilities:

Understand the regulatory framework, including regional trends, for various types of applications and procedures for small and large molecules across all regions.
Provide regulatory expertise on procedural and documentation requirements as defined by Health Authorities for assigned deliverable(s) including:
Submission delivery strategy of all dossiers and all application types per market and /or region
Review documents and provide regulatory input (e.g., response documents, high level documents, study protocols, Periodic Safety Reports, etc.)
Use and share guidelines, when handling various applications and procedures, while operating in a highly dynamic environment.
Lead and / or contribute to the planning, preparation and delivery of submissions of varying complexity throughout the product’s life cycle from either a global and/or regional perspective.
Lead multi-disciplinary project teams.
Develop, implement and maintain submission delivery plans, submission content plans, and proactively provide status updates to designated collaborators.
Identify regulatory risks and communicate mitigations to appropriate member of cross functional teams.
Support operational and compliance activities for assigned regulatory tasks.
Provide coaching, mentoring and knowledge sharing within the Regulatory Affairs Management skill group.
Contribute to process improvement.

Minimum Requirements – Education and Experience

Relevant University Degree in Science or related discipline
Extensive regulatory experience (5+ years) within the biopharmaceutical industry, or experience at a health authority
Thorough Knowledge of drug development
Strong project management skills
Leadership skills, including experience leading multi-disciplinary project teams

Preferred Experience

Knowledge of the Respiratory & Immunology therapy area.
Managed first wave Marketing Application and/or Life Cycle Management submissions
Managed complex regulatory deliverables across projects/products
Veeva Vault experience
Knowledge of AZ Business and processes
Demonstrate high ability to use AI digital tools and solutions

Skills and Capabilities

Excellent written and verbal communication skills
Cultural awareness
Scientific knowledge sufficient to understand regulatory issues and facilitate scientific discussions
Proficiency with common project management (e.g., MS Project) and document managementtools
Ability to work independently and as part of a team
Influencing and stakeholder management skills
Ability to analyze problems and recommend actions
Continuous Improvement and knowledge sharing focused

Are you interested in working at AZ, apply today!

AstraZeneca is committed to taking every reasonable precaution to protect employees, our customers and the healthcare systems in the communities in which we serve. In an effort to protect the wellbeing of our employees and customers, full COVID-19 vaccination is an essential requirement of all positions at AstraZeneca. As such, all offers of employment will be conditional upon either (i) proof of full COVID-19 vaccination or (ii) proof of need for accommodation under relevant human rights legislation, and AstraZeneca’s determination that the requested accommodation can be provided without undue hardship. You will be required to submit proof of full vaccination or proof of need for accommodation during our background screening process.

AstraZeneca is an equal opportunity employer that is committed to diversity and inclusion and providing a workplace that is free from discrimination. AstraZeneca is committed to accommodating persons with disabilities. Such accommodation is available on request in respect of all aspects of the recruitment, assessment and selection process and may be requested by emailing AZCHumanResources@astrazeneca.com.

⠀

Annual base salary for this position ranges from 133,311.20 to 174,970.95.

AstraZeneca is committed to providing fair and equitable compensation opportunities to all colleagues. Our compensation policies and practices have been designed to allow colleagues to progress through the salary range over time as they progress in their role. The range provided in this posting represents an offer pay range used in a majority of situations. The base pay offered will vary depending on multiple individualized factors, including the candidate's skills and experience, job-related knowledge, and other specific business and organizational needs. In some cases, offers outside the range may also be considered to address unique circumstances.

In addition, our permanent positions offer an annual Variable Pay Bonus/Short Term Incentive opportunity as well as eligibility to participate in our equity-based long-term incentive program (if applicable to role). Benefits offered for permanent roles include a competitive Flex Benefits & Retirement Savings Program, 4 weeks’ paid vacation, and annual Personal Days. Fixed Term Contract/Temporary positions (excluding students) are offered a Contract Benefits Program.

We are using AI as part of the recruitment process.

This advertisement relates to a current vacancy.

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More about this job

Responsibilities

The Associate Regulatory Affairs Director leads the end-to-end planning, coordination, and execution of regulatory submissions while providing expertise to cross-functional teams. They are responsible for identifying submission risks, managing complex regulatory applications, and ensuring compliance throughout the product life cycle.

Requirements

Candidates must hold a relevant university degree in science or a related discipline and possess at least 5 years of regulatory experience within the biopharmaceutical industry. Strong project management, leadership, and communication skills are essential for managing multi-disciplinary teams and regulatory deliverables.

Skills

Regulatory affairs
Project management
Submission strategy
Drug development
Leadership
Regulatory framework
Stakeholder management
Risk management
Coaching
Mentoring
Veeva Vault
MS Project
Communication
Scientific knowledge
Process improvement

Benefits

Flex Benefits
Retirement Savings Program
Paid vacation
Personal Days
Variable Pay Bonus
Short Term Incentive
Equity-based long-term incentive program

Visa sponsorship

Not detected in the job text

Keywords

Regulatory Affairs
Biopharmaceutical
Drug Development
Submission Strategy
Health Authorities
Dossiers
Periodic Safety Reports
Respiratory & Immunology
Marketing Application
Life Cycle Management
Veeva Vault
AI digital tools
MS Project
Compliance
Stakeholder Management
Cross-functional teams
Small molecules
Large molecules
Regulatory framework
Project planning

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