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Roche

Technology Product Owner

Posted 10 Hours Ago
Be an Early Applicant
In-Office
Mississauga, ON, CAN
Senior level
In-Office
Mississauga, ON, CAN
Senior level
The Technology Product Owner will standardize and optimize technology solutions for Quality operations in pharma. Responsibilities include lifecycle management of systems, business data stewardship, and driving product vision while collaborating with cross-functional teams.
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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 Specialist (PO) or Sub-Product Owner in Roche PT's Network Quality QA/QC Operational Systems 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. A core function of the role is translating complex business use cases and requirements into standardized, compliant technology solutions, requiring a blend of technical expertise and business acumen. The PO collaborates with cross-functional teams, including Business, IT, and Validation, to ensure that high-quality, innovative solutions are defined, developed, and implemented. The role also involves managing the global master data entity and assisting the organization with expertise during regulatory inspections and the resolution of deviations.

This position requires a collaborative and open-minded individual who is capable of maintaining and transforming integral technologies while valuing continuous learning. The successful candidate must be someone who thoughtfully challenges ideas, prioritizes impactful work, and can be relied upon to operate in the best interest of the team, thriving in a dynamic work environment.

The Opportunity:

  • You will standardize and optimize the systems and technology powering Quality operations and data insights.

  • You will translate complex business use cases and project requirements into standardized technology solutions.

  • You will serve as the Global Product Owner or sub-product owner for applicable technologies used in Pharma Technical Operations (PT).

  • You will lead the lifecycle management for multiple products and systems, including upgrades, replacement, and retirement of computerized systems.

  • You will manage system enhancement features, act as the Business Data Steward for data governance, and drive continuous improvement opportunities.

  • You will drive the product vision, roadmap, and development lifecycle.

  • You will provide in-depth global subject matter expertise and support the implementation of fit-for-purpose innovative solutions while ensuring GxP


Who you are :

  • You will have Bachelor's or Master's degree in Life Science, Computer Science, a related field, or an equivalent technical/vocational qualification.

  • Candidates must have 7+ years of experience in technology, systems, and platforms management within the pharmaceutical or healthcare industry.

  • Experience with validated or controlled environments is a requirement. Experience with Veeva Quality Vault (QMS, Quality Docs) and A/I are preferred.

  • Demonstrated proficiency in the Software Development Lifecycle is essential.

  • Knowledge of regulatory requirements (e.g., GMP, FDA) and Quality Systems is required.

  • Strong communication and collaboration skills are necessary to effectively convey findings and recommendations to both technical and non-technical audiences.

  • The role requires a technical foundation paired with business acumen and experience with Agile Methodologies

**Relocation not available for this position***

The expected salary range for this position based on the primary location of Mississauga is 115,328.00 and 151,368.00 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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