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Added 3 mins ago
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Be supported by a large and experienced Principal Engineering community
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The above statement reflects the general details considered necessary to describe principal functions of the job identified, and shall not be construed as a detailed description of all the…
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Laboratory Manager
The University of British Columbia
Vancouver, BC
$5,692.25 to $8,179.5 CAD / month
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Technology Product Owner Principal
Roche
Mississauga, ON · Canada Pharma Campus
Full-time
The Technology Product Owner Principal or Sub-Product Owner in Roche PT's Quality Processes Products team plays a pivotal role in standardizing and optimizing the systems and technology…
Added 6 hours ago
Laboratory Manager
University of British Columbia
Vancouver, BC · UBCV | Gordon B. Shrum Building (SHRM)
$5,692.25 to $8,179.5 CAD / month
Full-time
Reports directly to the Principal Investigator, Dr. Troy McDiarmid. Serves as the primary operational and scientific leader of the laboratory, functioning as a close partner to the PI in…
Added 6 hours ago
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Additional points: The job posting reflects the general details considered necessary to describe the principal functions and duties as required for proper evaluation of the job. There may…
Added 7 hours ago
Clinical Research Coordinator – Endometriosis Research Program
RI-MUHC | Research Institute of the MUHC | #rimuhc
Montreal, QC
Contract
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Project Manager, Capture and Optimization of Research Data (CORD) Platform
RI-MUHC | Research Institute of the MUHC | #rimuhc
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Full-time
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Research Associate
RI-MUHC | Research Institute of the MUHC | #rimuhc
Montreal, QC
Full-time
…leukodystrophies, and related disorders. Under the direction of the principal investigator, the candidate participates in the execution of various activities including expertise in iPSC…
Added 7 hours ago
MRI Technologist
RI-MUHC | Research Institute of the MUHC | #rimuhc
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Full-time
Ability to work closely with principal investigators and their study team,
Added 7 hours ago
Program Assistant – Cancer Research Program (CRP)
RI-MUHC | Research Institute of the MUHC | #rimuhc
Montreal, QC
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…admin team and will play a central role supporting up to 40 principal investigators and their research…
Added 7 hours ago
Research Assistant
RI-MUHC | Research Institute of the MUHC | #rimuhc
Montreal, QC
Temporary
…Research Program. The Research Assistant will report to the Principal Investigator and work closely with a multidisciplinary team of clinicians, data managers, statisticians, collaborators,…
Added 7 hours ago
MRI Technologist
RI-MUHC | Research Institute of the MUHC | #rimuhc
Montreal, QC
Full-time
Ability to work closely with principal investigators and their study team,
Added 7 hours ago
Laboratory Technician
RI-MUHC | Research Institute of the MUHC | #rimuhc
Montreal, QC
Full-time
Performs other related duties as required by the Principal Investigator.
Added 7 hours ago
Animal Resources Division Manager – Montreal General Hospital Site
RI-MUHC | Research Institute of the MUHC | #rimuhc
Montreal, QC
Full-time
…animal facilities. Assures constant quality of services to principal Investigators and their research staff and…

Roche

Technology Product Owner Principal

Mississauga, ON, Canada

Job type: Full-time
Apply by: Oct 21, 2026
Experience: You possess deep technical expertise: You bring 12+ years of experience in Veeva Quality Vault or equivalent Quality platform management - ideally Veeva QMS and Veeva Quality Docs
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

At Roche, we thrive to deliver more benefits to our patients as part of our 10-year Pharma vision. We serve our patients through external partnerships because access to quality products is every patient’s right. We leverage external partners in order to offer flexibility to our internal capacity at the right cost and quality. We enable our external partners to reliably deliver compliant, quality products to our supply chain customers, so that we can deliver to patients worldwide. We do this through cross-functional collaborations ensuring quality process excellence and continuous improvement.

The Technology Product Owner Principal or Sub-Product Owner in Roche PT's Quality Processes Products team plays a pivotal role in standardizing and optimizing the systems and technology that power Quality operations and data insights. The PO is responsible for defining and implementing the overall Technology strategy for PT Quality, acting as the Global Product Owner for applicable PT technologies.

The Oppurtunity:

Oversee large-scale, cross-functional systems that require understanding dependencies, integrations and long-term planning
Leads multiple products or complex technologies through the system lifecycle management process including change management
Influencing and directing the future innovation through opportunities with interdepartmental and industry collaborations
Translating complex business use cases and requirements into standardized, compliant technology solutions, requiring a blend of technical expertise and business acumen.
Champion cross-functional collaboration and ensure the team fosters strong partnerships with internal and external stakeholders. Focuses on multi-stakeholder alignment across teams.
Proactively identify opportunities to leverage technology innovations to improve business efficiency and outcomes. Drive the integration of technology-driven solutions to stay ahead in a competitive and rapidly changing industry landscape
Initiate, manage and close complex deviations, CAPAs or changes and support audits/ regulatory inspections as required. Define and monitor Key Performance Indicators (KPI’s) for IT System and product performance, efficiency and user satisfaction.
Serve as a global Principal Product Owner for QMS technologies (specifically Quality Vault QMS but can include Veeva Quality Docs ), effectively translating complex business requirements into standardized technical solutions. Manage the integration and structural nuances of the Veeva QMS and or Quality Docs ecosystem, ensuring seamless data flow, reporting, and interface connectivity across global manufacturing and commercial sites
Direct the entire system lifecycle - including upgrades, system replacements, and retirements - while strictly adhering to established change management processes
Partner closely with key Business Stakeholders and IT to define the product vision, align roadmaps, manage feature backlogs, and prioritize system enhancements
Act as the dedicated Business Data Steward, ensuring unwavering GxP compliance, strict data governance, and adherence to global quality policies
Mobilize and lead high-performing, cross-functional teams spanning global functions, sites, IT partners, and validation functions

Who You are:

You possess deep technical expertise: You bring 12+ years of experience in Veeva Quality Vault or equivalent Quality platform management - ideally Veeva QMS and Veeva Quality Docs
You are strategically and academically qualified: You hold a Bachelor’s or Master’s degree in Life Sciences, Computer Science, or a related field (or an equivalent qualification like a Federal Diploma of Higher Education) combined with a proven track record in formulating long-term computer system strategies
You are an expert in regulated environments: You possess a strong understanding of data integrity, data analytics, and software validation within validated or controlled pharmaceutical/healthcare environments (GMP, FDA, GxP)
You are an Agile collaborator and communicator: You are highly skilled at utilizing Agile methodologies and possess exceptional communication skills to convey technical findings and recommendations to both technical and non-technical audiences. You are an Agile collaborator, skilled at utilizing Agile methodologies to manage product backlogs and successfully adapting iterative delivery to meet strict computer system validation (CSV) and GxP release requirements
You are a proactive problem solver: You possess a technical foundation paired with sharp business acumen, allowing you to troubleshoot intricate system issues, navigate escalation paths and adapt setups to meet diverse site-specific needs.
Relocation not available for this position***

The expected salary range for this position based on the primary location of Mississauga is 136,936.00 and 179,728.50 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 Principal Product Owner defines and implements the global technology strategy for PT Quality, overseeing large-scale systems and product lifecycles. They lead cross-functional teams to standardize technology solutions while ensuring GxP compliance and continuous process improvement.

Requirements

Candidates must have 12+ years of experience in Veeva Quality platform management and a degree in Life Sciences, Computer Science, or a related field. Strong expertise in regulated pharmaceutical environments, Agile methodologies, and data integrity is required.

Skills

Veeva Quality Vault
Veeva QMS
Veeva Quality Docs
Product Ownership
Agile Methodologies
GxP Compliance
Computer System Validation
Data Governance
Change Management
System Lifecycle Management
Quality Process Excellence
Data Analytics
Stakeholder Management
Strategic Planning
Regulatory Inspections

Visa sponsorship

Not detected in the job text

Keywords

Veeva Quality Vault
Veeva QMS
Veeva Quality Docs
Product Owner
Agile
GxP
FDA
GMP
Computer System Validation
CSV
Data Integrity
Data Governance
Quality Management Systems
Change Management
CAPA
Deviations
System Lifecycle Management
Pharma
Biotechnology
Life Sciences
KPI
IT Strategy
Stakeholder Management
Regulatory Compliance
Business Acumen

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