Find work in Canada.

329,265 jobs across our Canadian network. How we count

Jobs in Canada

25+ jobs

Save this search

Added 1 hour ago
Supply Chain Operations Manager
CarbonRun
Dartmouth, NS
$80,000 to $100,000 CAD / year
Full-time
CarbonRun is hiring a Manager, Supply Chain Operations to lead feedstock sourcing, supplier management, and supply chain operations across our growing portfolio of river alkalinity…
Added 3 hours ago
Quality Assurance and Compliance Monitoring Officer - Civil Division-EN
CAE
Toronto, ON
Full-time
At CAE, our Safety, Quality Assurance and Compliance Monitoring team have in depth airline, regulatory and training expertise and are driven by excellence and strive for continuous…
Added 5 hours ago
Clinical Research Program Manager
Nova Scotia Health and IWK Health
Halifax, NS
Reporting to the study Principal Investigators, the Clinical Research Program Manager holds full operational, regulatory, and personnel oversight of the research program across the…
Added 6 hours ago
Manager, Compliance & Quality Standards
Municipality of Chatham-Kent
Chatham-Kent, ON · Chatham, ON
Full-time
Under the direction of the Director of Engineering & Compliance, the Manager of Compliance & Quality Standards provides leadership for compliance, quality management, environmental…
Added 15 hours ago
Medical Device Regulatory Specialist
Corvita Biomedical
Toronto, ON
Full-time
The Medical Device Regulatory Specialist will support Corvita's Health Canada-first regulatory program under the direct supervision of the Senior Regulatory Manager.
Added 15 hours ago
Early Talent Program Associate - PDR
Roche
Mississauga, ON · Canada Pharma Campus
Full-time
…meticulously crafted to impart comprehensive foundational knowledge in regulatory affairs. This dynamic initiative blends hands-on assignments with tailored learning solutions, making it an…
Added 2 days ago
Director of Engineering
Enova Power Corp.
Kitchener, ON
Full-time
…Management, and Supply Planning. The incumbent leads and directs the affairs of the Engineering department; ensures alignment with corporation vision, mission and strategic goals; provides…
Added 2 days ago
Non-Clinical Toxicology Manager
Alexion Pharmaceuticals, Inc.
Mississauga, ON
Full-time
Join us at Alexion, AstraZeneca's Rare Disease division, as a Non-Clinical Manager. You will be a key member of the non-clinical team in this role. You will collaborate with the global…
Added 6 days ago
Associate Product Manager
Loblaw Companies Limited
Brampton, ON
Full-time
Associate Product Manager, Enterprise Initiatives
Added 6 days ago
Coordinator, Education Programs & Communications
University of British Columbia
Vancouver, BC · UBCV | P. A. Woodward Instructional Resources Centre (IRC)
$6,143.67 to $8,830.25 CAD / month
Full-time
This position reports to the Manager, Strategic Initiatives at CIEBH and works collaboratively with the Senior Manager, CIEBH and other CIEBH and the office of research team members at the…
Added 3 days ago
Complaints Team Leader - Claims
Zego
Halifax, NS
Full-time
Work with Claims Technical, Underwriting, and Legal & Regulatory Affairs on coverage, avoidance, or legal risk complaints
Added 2 days ago
Senior Privacy & Compliance Manager
123Dentist
Toronto, ON · Boucherville, QC
$135,000 to $165,000 CAD / year
Full-time
…support and resources, including accounting, HR, operational, regulatory, marketing, legal, as well as supply and equipment procurement. By leveraging our unmatched management experience,…
Added 3 days ago
Senior Policy Analyst
Agriculture Financial Services Corporation
Olds, AB · Ponoka, AB · Medicine Hat, AB · Lacombe, AB · Stettler, AB · Leduc, AB · Red Deer, AB · Strathmore, AB · Drumheller, AB · Camrose, AB · Edmonton, AB · Grande Prairie, AB · Calgary, AB · Lethbridge, AB · AB
Reporting to the Manager, Lending Products and FPT Policy, the Senior Policy Analyst provides leadership, coordination, development, and knowledge/skill transfer to internal and external…
Added 2 days ago
Communications Specialist
BC Energy Regulator
Fort St. John, BC
Full-time
Chief Legal Counsel, Governance & Regulatory Affairs
Added 3 days ago
General Manager
3G4 Archive Hospitality
Toronto, ON
$110,000 to $120,000 CAD / year
Full-time
Position: General Manager, The Broadview Hotel
Added 2 days ago
Gestionnaire associé(e), Accès au marché / Associate Manager, Market Access
Knight Therapeutics Canada
Montreal, QC
Full-time
We are seeking an Associate Manager, Market Access, to join our Commercial team. Reporting to the Director, Market Access, this individual will lead and execute market access, pricing, and…
Added 3 days ago
Diabetes Clinical Research Coordinator (DCRC)
The University of British Columbia
Vancouver, BC
$29.82 to $35.16 CAD / hour
Full-time
With the assistance of the PI, liaise with the University/Industry Liaison Office (UILO) and BCCH Research Institute Finance Manager on contract related start-up issues
Added 3 days ago
Senior AI Risk Officer
BMO
Toronto, ON · FCP
Full-time
The Senior Manager, AI Risk (Audit & Regulatory Affairs Lead), operating within the second line of defense (Operational Non-Financial Risk), is responsible for overseeing AI risk management…
Added 3 days ago
Director, Regulatory Affairs (Canada)
GRIFOLS, S.A.
Toronto, ON · ON-Toronto, AB
Supervises: Departmental Supervisor for: Regulatory Affairs Manager
Added 3 days ago
Senior Manager, Trade Compliance
BMO
Toronto, ON · FCP
Full-time
Typically 9+ years of experience in Compliance, Trade Surveillance, Market Risk, Trade Operations, Regulatory Affairs, Internal Audit, or Capital Markets Controls.
Added 3 days ago
RCI-KVUE1-833 Manager, Communications
Rangam
Toronto, ON · North York, ON
$40 to $42 CAD / hour
Contract
Manager level, supporting a Consumer Health business in Canada; hybrid in Toronto/North York (approx. 2 days onsite).
Added 3 days ago
Senior Specialist, HVAC
City of Brampton
Brampton, ON
Full-time
Co-ordinates municipal response to Code change submission requests from the Ministry of Municipal Affairs and Housing.
Added 3 days ago
SENIOR SPECIALIST PLUMBING
City of Brampton
Brampton, ON
Full-time
Co-ordinates municipal response to Code change submission requests from the Ministry of Municipal Affairs and Housing.
Added 3 days ago
Clinical Research Coordinator I
University Health Network
Toronto, ON
Contract
Coordinating with the Project Manager to execute administrative tasks, such as collection of regulatory documents, ethics submissions and general paperwork
Added 3 days ago
Non-Clinical Toxicology Manager
AstraZeneca
Mississauga, ON · Canada - Mississauga
Full-time
Join us at Alexion, AstraZeneca's Rare Disease division, as a Non-Clinical Manager. You will be a key member of the non-clinical team in this role. You will collaborate with the global…

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

Apply About employer

Applications open in a new tab.

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.

Apply About employer

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

Report this job