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Added 1 hour ago
AI Architect, Manager
Avanade
Toronto, ON
Full-time
…environmental requirements. The AI Architect takes ownership of technology related aspects of AI across the Microsoft…
Added 1 hour ago
Managed Account Program (MAP) Support Specialist
Aviso
Toronto, ON
$60,000 to $70,000 CAD / year
Full-time
We're looking to fill an opening for a Managed Account Program (MAP) Support Specialist to join our Operations team.
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Finance Project Transformation Senior Associate
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As a risk management generalist at PwC, you will provide advisory and practical support to teams across a wide range of specialist risk and compliance areas.
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Senior Bilingual Talent Acquisition Specialist (People and Culture) (Telework/Hybrid)
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Full-time
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Added 3 hours ago
Early Talent Program Associate - APQR
Roche
Mississauga, ON · Canada Pharma Campus
Full-time
Support the generation of performance metrics, overall quality assessments, and automated reporting tools.
Added 3 hours ago
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Business Analyst - Junior - RQ00692
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S M Software Solutions Inc
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UX Researcher – Senior - RQ00786
S M Software Solutions Inc
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UX Researcher – Senior - RQ00786
S M Software Solutions Inc
Toronto, ON
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We are looking for an experienced UX Researcher – Senior to support CX/UX activities across the Patients Before Paperwork (Pb4P) initiative within the Ontario Health environment. The ideal…
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Roche

Early Talent Program Associate - APQR

Mississauga, ON, Canada
Canada Pharma Campus, Canada

Job type: Full-time
Workplace: Hybrid
Apply by: Oct 3, 2026
Experience: You bring up to 1 year of relevant post-degree pharmaceutical experience, with foundational knowledge of GMPs, industry regulations, and technical writing.
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

The Quality Process Management team drives strategic design, continuous improvement, and compliance across our Quality Management System to deliver best-in-class pharmaceutical products. As an Intern / Early Talent Program Associate in Quality Process Management focusing on the Annual Product Quality Review (APQR), you will gain foundational experience in regulatory compliance, quality systems, and data-driven cross-functional collaboration. This role offers hands-on exposure to global operations with guidance and mentorship designed to accelerate your technical and professional growth.

The Opportunity

Assist in compiling and preparing global quality reviews by analyzing and visualizing product data from multiple enterprise systems.
Evaluate product quality data to identify emerging trends, mitigate operational risks, and recommend continuous improvement opportunities.
Support the generation of performance metrics, overall quality assessments, and automated reporting tools.
Collaborate with cross-functional global stakeholders to ensure data accuracy, meet project timelines, and resolve quality-related issues.
Maintain Quality Management System documentation, records, training materials, and annual schedules to ensure audit readiness.
Participate in team discussions through active listening, open communication, and constructive, problem-solving engagement.
Perform assigned quality oversight tasks in full alignment with global health authority regulations, GMP standards, and company procedures.

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 possess a basic understanding of drug development processes and an entry-level understanding of the role of a regulatory professional.
You bring up to 1 year of relevant post-degree pharmaceutical experience, with foundational knowledge of GMPs, industry regulations, and technical writing.
You are an analytical thinker with strong attention to detail, basic statistical skills, and comfortable working with technology platforms and data visualization.
You are a proactive team player and clear communicator who thrives in global interdisciplinary environments and takes ownership of your personal learning.

Additional Information:

Division: Pharma
Department: Annual Product Quality Review (APQR).
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.
Aproximate start date in January 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.

#OneAPQR

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 assist in compiling and analyzing global product quality data to identify trends and support continuous improvement initiatives. They will also maintain Quality Management System documentation and collaborate with stakeholders to ensure audit readiness and regulatory compliance.

Requirements

Candidates must hold a degree in life sciences, biological sciences, chemistry, or pharmacy completed within the last two years. Applicants should possess foundational knowledge of GMPs, industry regulations, and basic statistical skills.

Skills

Regulatory Compliance
Quality Management Systems
Data Analysis
Data Visualization
Technical Writing
GMP
Pharmaceutical Operations
Statistical Skills
Cross-functional Collaboration
Performance Metrics
Audit Readiness
Problem-solving
Drug Development
Quality Oversight

Visa sponsorship

Not detected in the job text

Keywords

APQR
Quality Management System
Regulatory Compliance
Pharmaceutical
GMP
Data Visualization
Technical Writing
Quality Oversight
Life Sciences
Chemistry
Biology
Pharmacy
Audit Readiness
Performance Metrics
Drug Development
Continuous Improvement
Operational Risk
Global Operations

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