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Roche

Early Talent Program Associate - PDR

Mississauga, ON, Canada
Canada Pharma Campus, Canada

Job type: Full-time
Workplace: Hybrid
Apply by: Oct 3, 2026
Experience: Maximum 1 year relevant pharmaceutical experience post last degree
Working hours: 35 hours per week
Posting language: English
Posted: Sep 21, 2026

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Original job description

At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.

The Position

Embark on a transformative two-year journey with the One PDR ET Program, meticulously crafted to impart comprehensive foundational knowledge in regulatory affairs. This dynamic initiative blends hands-on assignments with tailored learning solutions, making it an ideal entry-point for aspiring regulatory professionals. Eligible candidates should possess a Bsc in life or pharmaceutical sciences, or an equivalent scientific qualification, and have less than one year of relevant pharmaceutical regulatory experience. Participants gain invaluable insights into the complete lifecycle of pharmaceutical products, from initial clinical trials to market exit, by engaging in diverse activities across various therapeutic areas and stages of development. The latter part of the program offers the opportunity to rotate into another Product Development function or specialize further in PDR.

Throughout the program, ETs collaborate with global drug development teams to support the introduction of novel pharmaceutical products to patients worldwide. This environment not only enhances their scientific writing skills but also deepens their understanding of regulatory frameworks by preparing a wide array of regulatory documents. By joining the One PDR ET Program, participants become pivotal contributors to the regulatory landscape, dedicated to ensuring that life-changing medicines reach those who need them most.

The opportunity:

Delivers on projects with mentorship and actively builds foundational regulatory experience with the support of colleagues.
Owns their learning and development, actively seeking to understand drug development and regulatory roles, and engaging in knowledge sharing and peer support.
Responsible for understanding and applying business processes to deliver foundational regulatory deliverables.
Engages with the team through active listening, practicing open communication, and building trust within regulatory and cross-functional teams.
Grasps the vision of the Roche organization, understanding how their work impacts the team and contributes to overall goals.
Improves prioritization and time management skills while spending significant time on-site at Roche/Genentech offices.

Who you are:

You hold a minimum qualification of a first degree in a life sciences, biological sciences, biology, chemistry, Pharmacy, or related field before the start of the program from which you have graduated from within the past 2 years. And you are within two years of completion of a degree program in the before mentioned disciplines.
You have basic understanding of drug development and entry level understanding of the role of a regulatory professional
Maximum 1 year relevant pharmaceutical experience post last degree
Demonstrates a learning mentality, engages in personal growth, and actively seeks and acts on feedback.
Fosters partnership, collaboration, empowerment, and autonomy to build a strong community.

Additional Information:

Division: Pharma
Department: Global Product Development Regulatory (PDR)
Reports to: Functional/Senior Functional Manager
Location: Hybrid, Based in Mississauga, ON
Hours: full-time (35 hours per week)
Length: This opportunity is a 2-year work term.
Approximate start in September 2027.

The statements made in this job description are intended to describe the general nature and level of work being performed by those persons assigned to this job. These statements are not intended to be a comprehensive list of all responsibilities, duties and skills required of people assigned to this job.

#onepdr

This position is not eligible for relocation support.

The expected salary range for this position based on the primary location of Mississauga is 71 544,00 and 93 901,50 of hiring range. Actual pay will be determined based on experience, qualifications, and other job-related factors as determined by the company.

We use artificial intelligence to screen, assess or select applicants for this role.

This posting is for an existing vacancy at Hoffmann-La Roche Ltd.

Who we are

A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.

Let’s build a healthier future, together.

Roche is an Equal Opportunity Employer.

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More about this job

Responsibilities

The associate will support global drug development teams by preparing regulatory documentation and applying business processes to foundational deliverables. They will also engage in cross-functional collaboration and participate in rotations across various product development functions.

Requirements

Candidates must hold a bachelor degree in life sciences, pharmacy, or a related field, earned within the last two years. Applicants should have less than one year of relevant pharmaceutical regulatory experience and demonstrate a strong learning mentality.

Skills

Regulatory affairs
Drug development
Scientific writing
Regulatory frameworks
Project management
Time management
Communication
Collaboration
Active listening
Data analysis
Pharmaceutical research
Clinical trials

Visa sponsorship

Not detected in the job text

Keywords

Regulatory Affairs
Pharmaceutical Sciences
Drug Development
Clinical Trials
Regulatory Frameworks
Product Development
Life Sciences
Biology
Chemistry
Pharmacy
Regulatory Documentation
Global Drug Development
Project Delivery
Mentorship
Regulatory Compliance

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