Roche Posted September 21, 2026

Technology Product Owner Principal

Mississauga, Ontario, Canada Full time
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About this opportunity

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.

Job details

Seniority
Principal
Function
Information Technology
Therapeutic area
Not listed
Location
Mississauga, Ontario, Canada
Employment type
Full time

How this role compares

Computed from every other active Information Technology role in our database, not just this employer's listings.

We currently track 379 comparable Principal Information Technology roles across 49 biopharma companies.

379Comparable roles tracked
359Currently active
49Companies hiring similar roles
27Countries represented

Salary context

57 of 379 peers report a salary range (USD, annualized)

Peers share this role's job function and a matching or adjacent seniority level -- not necessarily the same therapeutic area or country.

This roleSubject Not listed on this posting
Highest disclosed · Sr. AI Science Lead · Lilly $267,000/yr – $391,600/yr
Peer group range $98,050 – $329,300 (median $187,500)

Where these roles are based

Top locations among the 379 comparable roles

India180
United States110
Spain21
Poland10
Portugal8
Greece5

+ 21 more countries

Seniority mix

379 of 379 peers have a known seniority level

Senior272
Principal66
Director41

Therapeutic area mix

2 of 379 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Oncology1
Vaccines & Infectious Disease1

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Get an email when we spot other openings like this one – same job function, comparable seniority, roles you'd actually want to see.

How we calculate "similar"

No black box, no LLM guesswork: a deterministic score built from four normalized attributes. Here's this role's own peer group at different match levels, so you can see the mechanism, not just the result.

Every comparison starts from the same 100-point budget: 25 for working in the same function, 40 for the same therapeutic area, 20 for the same or adjacent seniority, 15 for the same country. A dimension we can't confirm on both sides contributes nothing, never a guess, never a free pass.

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Unmatched or unknown dimensions score exactly the same: 0 points, never a partial guess. A role we know almost nothing about beyond its function bottoms out at 25%; it never inflates to 100% just because there's little to compare against. Seniority uses a defined ladder (Associate → Manager → Associate Director → Senior → Principal → Director → Senior Director → Executive/VP) so "Director" and "Senior Director" count as adjacent, but "Director" and "Executive/VP" do not.