Roche Posted October 27, 2026

Staff Systems Engineer

Tucson, Arizona, United States of America FULL_TIME
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Roche is the source of truth for this posting and owns the application process. We surface normalized context and market comparison you won't find on the original listing.

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

A healthier future. It’s what drives us to innovate. To continuously advance science and ensure everyone has access to the healthcare they need today and for generations to come. Creating a world where we all have more time with the people we love. That’s what makes us Roche.

This Staff Systems Engineer position will primarily drive system integration efforts for next generation staining systems. This position is a highly skilled technical specialist responsible for applying intensive and diversified knowledge of systems engineering design principles, practices and implementation in complex systems and assignments. General responsibilities of the position include V-Model deliverables of systems engineering, participating in design reviews, development and testing to assess performance against design specification and assessment of system interactions. The position ensures assays work efficiently & effectively with the latest technologies and systems.

The Opportunity:  

Partners with business stakeholders and systems development teams to translate customer needs into effective design inputs & outputs.

Works with multi-functional teams, including R&D, Marketing, Operations, Quality, and Regulatory to ensure alignment with organizational objectives and regulatory requirements.

Executes project deliverables specific to requirements, risk, configuration management, defect management, and verification and validation in the company specific tool.

Demonstrates ability to integrate systems including automated staining systems, scanners, and software updates.

Plans integration roadmaps, defines integration frameworks, and manages architecture specifications throughout the development lifecycle.

Defines integration test plans, manages test cases, and coordinates environment setups for troubleshooting and interface validation.

Acts as the bridge between technical engineering teams, project managers, solution architects, and business stakeholders.

Diagnoses data flow breakdowns, resolves system conflicts, and delivers minor enhancements or defect fixes.

Establishes measurable criteria for Agile User Stories and Features, formally accepts work on behalf of the Program, and ensures they meet the agreed-upon Definition of Done.

Breaks down Agile Features into smaller, independent User Stories for seamless and incremental delivery.

Engages actively in Agile processes, including iteration planning, daily sync-ups, retrospectives, and Inspect and Adapt events to drive continuous improvement.

Presents system demos, delivers compelling presentations to stakeholders, and upholds a commitment to First-Time Quality in all project outcomes.

Who You Are

You possess a Bachelor's Degree in a directly related discipline + 8 years of related experience, OR MS degree in a directly related discipline + 6 years of related experience, OR PhD degree in a directly related discipline + 3 years of related experience.

You have experience working in a regulated environment demonstrating familiarity with FDA, ISO, IVD, and other relevant regulatory standards for diagnostic products.

You possess proven expertise in requirements management, system design, user experience development, and usability with the ability to mentor others in these practices.

You possess the ability to translate business requirements and customer needs into actionable system design inputs while balancing alternatives and managing expectations.

You possess expertise in translating stakeholder needs into structured, traceable, and compliant technical baselines using recognized international frameworks and industry guidelines.

You possess the ability to communicate technical risk, tradeoffs and investment needs clearly to engineering, product and senior business stakeholders.

You possess expertise in system integration techniques by bridging the gap between assay, hardware, consumables, software, sub-assemblies, or enterprise systems to ensure they work together as a cohesive system.

You possess strong systems thinking capabilities, creativity, and effective collaboration with technical teams to deliver optimized designs aligned with business needs and technological constraints.

You possess proficiency in prioritizing work based on evidence, applying lean design principles, and actively engaging team feedback before decision-making.

Preferred Qualifications

Understanding of Path Lab advanced staining functionality, slide workflows, use-cases of hardware & pre-filled consumables in the lab.

Ability to plan, define & develop characterization protocols and DoEs to derive meaningful conclusions.

Experience to build authority and accountability within a team with strong collaboration and communication skills.

Excellent organizational skills, including the ability to efficiently evaluate, prioritize and handle multiple priorities.

Familiarity with the assay development & manufacturing processes.

Ability to influence others to get a consensus on the best solutions for Roche and the customer.

Ability to challenge existing designs or practices and think outside the box to be innovative in problem solving. Possess a mindset of taking initiatives in not only tackling, but following through on hard problems.

This is an on-site position based in Tucson, AZ

Relocation benefits are not available for this posting.

The expected salary range for this position based on the primary location of  Tucson, Arizona is 110,700-205,700USD annually. Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law. A discretionary annual bonus may be available based on individual and Company performance.

This position also qualifies for the benefits detailed at the link provided below.

Benefits

 

 

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. It is our policy and practice to employ, promote, and otherwise treat any and all employees and applicants on the basis of merit, qualifications, and competence. The company's policy prohibits unlawful discrimination, including but not limited to, discrimination on the basis of Protected Veteran status, individuals with disabilities status, and consistent with all federal, state, or local laws.

If you have a disability and need an accommodation in relation to the online application process, please contact us by completing this form Accommodations for Applicants .

Job details

Seniority
Not listed
Function
Manufacturing & CMC
Therapeutic area
Not listed
Location
Tucson, Arizona, United States of America
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 3428 comparable Manufacturing & CMC roles across 175 biopharma companies.

3428Comparable roles tracked
3174Currently active
175Companies hiring similar roles
61Countries represented

Salary context

813 of 3428 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
Lowest disclosed · Operator – Plant Utilities · Lilly $13/hr – $28/hr (≈ $26,998–$58,302/yr)
Highest disclosed · Head of Analytical Development · ModernaTX, Inc. $272,200/yr – $490,100/yr
Peer group range $42,650 – $381,150 (median $127,400)

Where these roles are based

Top locations among the 3428 comparable roles

United States1570
Germany211
India155
France149
Ireland129
China125

+ 55 more countries

Seniority mix

1516 of 3428 peers have a known seniority level

Senior408
Manager359
Intern/Fellow/Postdoc208
Associate149
Principal129
Associate Director105
Director104
Senior Director48
Executive/VP6

Therapeutic area mix

22 of 3428 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Vaccines & Infectious Disease13
Rare Disease3
Dermatology & Aesthetics2
Oncology2
Immunology1
Respiratory1

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
40%similar
Lilly Indianapolis, Indiana, United States of America Director
Same function Same country
40%similar
Lilly Indianapolis, Indiana, United States of America Associate
Same function Same country
40%similar
Merck West Point, Pennsylvania, United States of America Principal
Same function Same country
40%similar
Merck West Point, Pennsylvania, United States Intern/Fellow/Postdoc
Same function Same country
40%similar
AbbVie North Chicago, IL Associate Director
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%
Director, Global Regulatory Affairs – Chemistry, Manufacturing and Controls (CMC), Platform Innovation – Synthetic Peptides and Oligonucleotides
Lilly · Indianapolis, Indiana, United States of America · Director
Function Therapeutic area Seniority Country
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Merck · West Point, Pennsylvania, United States of America · Principal
Function Therapeutic area Seniority Country
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AbbVie · North Chicago, IL · Senior
Function Therapeutic area Seniority Country
40%
Senior Scientist, II Biologics & Genetic Medicine - LCMS Characterization & Bioanalysis
AbbVie · North Chicago, IL · Senior
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.