Roche Posted October 7, 2026

Product Owner - DDS Pathology Lab

Warsaw, Masovian, Poland 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

Product Owner - DDS Pathology Lab

As the Product Owner - DDS Pathology Lab, you will drive the design and definition of next-generation software systems that empower diagnostic pathology. In this role, you will apply deep expertise in software systems design architecture to translate complex customer workflows into precise technical design specifications. Serving as a servant leader to an agile team, you will own the delivery of design inputs, champion concept generation, and ensure final software deliverables meet rigorous quality standards and real-world clinical outcomes in a collaborative, self-organizing environment.

The Opportunity:

Partner closely with business and software development teams to translate high-level business objectives, customer requirements, and user needs into clear, detailed software design specifications.

Interact regularly with implementation teams to ensure delivered features align with design specifications and the overall product architectural vision, providing technical guidance as needed.

Manage, refine, and prioritize the product backlog in collaboration with business stakeholders, ensuring user stories are well-defined, estimated, and aligned with project goals.

Facilitate backlog grooming and Program Increment (PI) planning sessions, defining clear acceptance criteria for user story acceptance and completion.

Provide development teams with detailed design specifications developed in collaboration with Program Management and System Architects, empowering teams to operate independently and effectively.

Apply deep expertise to elicit, evaluate, specify, and validate requirements for complex software systems, ensuring complete documentation, traceability, and alignment with business goals.

Develop comprehensive use cases capturing functional requirements, user interactions, alternate flows, exception handling, system integration complexities, and edge cases.

Define activity diagrams, user interactions, and acceptance criteria that clearly communicate intended system behavior to both technical and non-technical stakeholders.

Champion customer centricity, built-in software quality, holistic system design thinking, and technical excellence across development teams.

Present complex technical data, design concepts, and product backlog strategies to diverse internal and external audiences, while reviewing and critiquing team presentations.

Consult on software systems design and development issues, contributing to strategic direction and driving creative technology applications.

Model a constructive and professional speak-up culture within a self-organizing team environment.

Monitor work to drive a "Quality First Time" mindset, ensuring strict compliance with medical device software lifecycle standards (e.g., IEC 62304) and digital pathology workflows.

Qualifications:

Demonstrated subject matter expertise in complex software systems, systems thinking, creativity, critical thinking, and collaborative problem-solving.

Proven ability to translate business requirements and customer needs into robust software design using expert practices in requirements management, systems design, user experience (UX) development, and usability.

Demonstrated track record of mentoring team members in requirements management, systems design, user experience development, and usability best practices.

Ability to influence cross-functional teams and build consensus around optimal solutions that align customer value with business goals.

Deep understanding of internal company design practices, combined with the ability to apply industry best practices and external benchmarks.

Skilled in prioritizing engineering effort based on empirical evidence, data-driven decisions, and lean design principles.

Strong communication skills with a proven ability to listen attentively to stakeholder concerns before offering recommendations or decisions.

Knowledge of information security and data privacy fundamentals.

Willingness and ability to travel based on business needs.

English: Full Professional Proficiency

Preferred Qualifications:

Ability to manage stakeholder expectations when balancing complex design alternatives against business, budget, and technical constraints.

Demonstrated proficiency in documenting software systems design using Unified Modeling Language (UML).

Recognized reputation as a domain subject matter expert, demonstrated by sustained performance and significant career accomplishments.

SAFe® Product Owner/Product Manager (POPM) certification or equivalent Scaled Agile Framework experience.

What you get:

Competitive salary based on the employment contract.

Annual bonus payment based on your performance.

Hybrid Work Model: 2 days per week in the Warsaw office

Comprehensive benefits: Private healthcare (LuxMed), group life insurance (UNUM), Multisport card

Generous leave programs: Recharge Fridays (2 extra Fridays off per quarter), Take Time Program (up to 3 months), Take Time for Charity (up to 2 weeks)

Global work options: Flex Location for extended periods anywhere in the world

Additional perks: Stock share purchase options, company equipment sales, and more!

Interested? Apply!

The controller of your personal data is Roche Polska Sp. z o.o., ul. Domaniewska 28, 02-672 Warsaw. The data is processed for the purpose of recruitment. You have the right to access your data, rectify it, delete it, limit processing, transfer it and - if processing is based on your consent - withdraw this consent at any time. Contact the Data Protection Officer at: Ochrona.danych@roche.com. More information on the principles of processing your personal data by Roche at the link: https://www.roche.pl/pl/content/klauzula-informacyjna-rekrutacja-en.html

Roche Polska sp. z o.o.  operates in full compliance with the law and does not tolerate any violations. Roche  Polska sp. z o.o.  has implemented a Procedure for Reporting Violations of Law. If you wish to report any irregularities related to our activities, all necessary information regarding the reporting process can be found on our website: https://www.roche.pl/kontakt/ochrona-sygnalistow-zglaszanie-naruszen .

Compensation & Benefits

Where pay transparency applies, details are provided based on the primary posting location. For this role, the primary location is Warsaw. If you are interested in additional locations where the role may be available, we will provide the relevant compensation details later in the hiring process.

Information about the compensation package for this position will be provided ahead of any interview

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
Not listed
Function
Manufacturing & CMC
Therapeutic area
Not listed
Location
Warsaw, Masovian, Poland
Employment type
FULL_TIME

How this role compares

Computed from every other active Manufacturing & CMC role in our database, not just this employer's listings.

We currently track 3720 comparable Manufacturing & CMC roles across 172 biopharma companies.

3720Comparable roles tracked
3319Currently active
172Companies hiring similar roles
64Countries represented

Salary context

906 of 3720 peers report a salary range (USD, annualized)

Peers share this role's job function. This posting doesn't list a seniority level, so peers aren't narrowed by seniority either -- the range below may span more levels than usual.

This roleSubject Not listed on this posting
Highest disclosed · Head of Analytical Development · ModernaTX, Inc. $272,200/yr – $490,100/yr
Peer group range $0 – $381,150 (median $126,575)

Where these roles are based

Top locations among the 3720 comparable roles

United States1724
Germany246
India162
France148
Ireland133
China121

+ 58 more countries

Seniority mix

1647 of 3720 peers have a known seniority level

Senior429
Manager374
Intern/Fellow/Postdoc251
Associate165
Principal134
Director118
Associate Director114
Senior Director53
Executive/VP9

Therapeutic area mix

24 of 3720 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Vaccines & Infectious Disease15
Rare Disease3
Oncology3
Respiratory1
Dermatology & Aesthetics1
Immunology1

Similar opportunities

The closest matches from our peer group, ranked by how similar they are, not how well you'd qualify for them -- treat this as market context, not a guaranteed shortlist; a weak match is labeled as one below.

40%similar
Bayer Warszawa, Poland Senior
Same function Same country
40%similar
Bayer Warszawa, Poland Manager
Same function Same country
40%similar
Sandoz Strykow, Poland
Same function Same country
40%similar
Sandoz Warsaw, Poland
Same function Same country
40%similar
40%similar
Sandoz Strykow, Poland
Same function Same country

Notify me about similar jobs

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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.

40%
Senior Integration Architect - Manufacturing (Warszawa, Mazowieckie, PL)
Bayer · Warszawa, Poland · Senior
Function Therapeutic area Seniority Country
40%
Supply and Inventory Planner
Sandoz · Warsaw, Poland · Seniority not listed
Function Therapeutic area Seniority Country
40%
Senior Manager, Procurement, Research & Development
E.R. Squibb & Sons,L.L.C. · Warsaw, Poland · Manager
Function Therapeutic area Seniority Country
40%
Młodszy(-a) Operator(-ka) Urządzeń
Teva Pharmaceuticals · Kraków, Poland · Seniority not listed
Function Therapeutic area Seniority Country
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.