Roche Posted August 11, 2026

Principal Automation Research Engineer, Next Gen Sequencing Systems

Santa Clara, California, United States of America FULL_TIME
Manufacturing & CMC Principal

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

At Roche, we are developing the next-generation of sequencing systems. By accelerating clinical research, streamlining workflows, and expanding assay menus, we are also broadening access to genomic data and lowering barriers to adoption. From robust sample isolation and preparation tools to novel sequencing technology and advanced bioinformatics, we are developing differentiated, highly integrated end-to-end solutions for next-generation sequencing workflows.

Our Workflow Automation R&D Group, a part of Roche Sequencing Solutions, is focused on enhancing sequencing workflows. We are seeking a highly collaborative Principal Automation Research Engineer to contribute to the research and development of current and future automated platforms, while simultaneously building the tools to democratize key processes and eliminate bottlenecks.

This is a hands-on, multidisciplinary role focused on solving automation challenges, integrating AI tools to streamline workflows, and tackling the fluidic, mechanical and consumables challenges at the heart of our next-generation platforms. We are looking for someone who exhibits a high degree of motivation, independence, and resourcefulness to help us develop solutions to our automation challenges in a fast-paced and collaborative environment.

Core Responsibilities

You will utilize AI-assisted coding and modern software development tools to accelerate protocol generation, protocol simulation, debugging, test suite development, and automated error recovery.

You will translate complex manual workflows (i.e. sample prep, library prep, target enrichment, quantification, pooling, and sequencing) into highly reliable automated scripts.

You will test scripts and validate system performance through various analytical equipment and data analysis pipelines

You will contribute to architecture, design, research and development of next-generation automation platforms. Design, build, assemble and operate custom test fixtures to support testing of these platforms, modules and sub-systems.

You will translate high-level system and assay requirements into fluidic schematics, system architectures and concepts to evaluate, compare, and downselect design paths.

You will create and maintain comprehensive documentation for all work, from requirements, schematics, diagrams, CAD models, manufacturing drawings, and material specifications.

You will partner directly with Assay Development Scientists, Hardware Engineers, Software Developers, and Product Managers to align platform functionality with customer requirements. Conduct cross-functional concept, code/script and design reviews. Present progress, data, and engineering decisions clearly to stakeholders.

This position is based on-site in Santa Clara, CA. (This is not a hybrid position. There will be some travel to our Roche Pleasanton (CA) site.)

Relocation benefits are not being offered for this role.

Please include a cover letter with your application.

Who You Are:

(Required)

You have a degree in Bioengineering or Biomedical Engineering, or a closely related discipline, with relevant industry experience (7+ years for a Bachelor's, 5+ years for a Master's, or 3+ year for a PhD).

You have a demonstrated level of In-depth understanding of chemistry and molecular biology, specifically sequencing chemistry and workflows

You have demonstrated hands-on experience characterizing and testing complex automation systems for sequencing or diagnostics.

You have demonstrated hands-on experience using modern AI-assisted tools to accelerate code generation, parse schemas, and automate test cases.

You have demonstrated experience with markup and programming languages (e.g., XML, Python, or proprietary scripting environments) used to define automated instrument steps and hardware execution.

You have a solid level of experience in experimental design

You have a demonstrated level of proficiency with machine shop tools, measurement equipment, and rapid prototyping technologies.

You have demonstrated experience troubleshooting, with a solid understanding of physics, chemistry and engineering fundamentals.

Preferred Qualifications:

You have experience with DNA sequencing, DNA synthesizers and other complex fluidic automation instrumentation.

You have a demonstrated track record of acting as a bridge between scientists and the hardware/consumables engineers.

You have excellent organizational skills with the ability to manage multiple project tracks efficiently and thrive in ambiguous, fast-paced environments.

You have experience working with a sense of urgency, contagious optimism, and natural curiosity regarding technical, business, and market trends.

You have demonstrated experience in SolidWorks for part design, detailed assembly design and the creation of manufacturing drawings.

The expected salary range for this position based on the primary location of Santa Clara, CA is $110,600 - $205,500.  Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law.  We encourage all qualified applicants to apply. The role's level (& title) may be adjusted based on experience and qualifications. 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
Principal
Function
Manufacturing & CMC
Therapeutic area
Not listed
Location
Santa Clara, California, 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 393 comparable Principal Manufacturing & CMC roles across 56 biopharma companies.

393Comparable roles tracked
368Currently active
56Companies hiring similar roles
19Countries represented

Salary context

189 of 393 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
Lowest disclosed · Senior Scientist II – CMC Developmental Sciences · AbbVie $0/hr – $0/hr (≈ $0–$0/yr)
Highest disclosed · Director, Global Automation Engineering · AbbVie $182,000/yr – $346,000/yr
Peer group range $0 – $264,000 (median $150,600)

Where these roles are based

Top locations among the 393 comparable roles

United States282
India42
Singapore10
Ireland9
Netherlands7
Switzerland6

+ 13 more countries

Seniority mix

393 of 393 peers have a known seniority level

Senior251
Principal78
Director64

Therapeutic area mix

2 of 393 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Oncology1
Vaccines & Infectious Disease1

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.

60%similar
Lilly Indianapolis, Indiana, United States of America Principal
Same function Same seniority Same country
60%similar
Lilly Louisville, Colorado, United States of America Principal
Same function Same seniority Same country
60%similar
Lilly Indianapolis, Indiana, United States of America Principal
Same function Same seniority Same country
60%similar
Lilly Watertown, Massachusetts, United States of America Principal
Same function Same seniority Same country
60%similar
Lilly Indianapolis, Indiana, United States of America Principal
Same function Same seniority Same country
60%similar
Lilly Indianapolis, Indiana, United States of America Principal
Same function Same seniority Same country

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.

60%
Senior/Principal Scientist, Bioprocess Purification Development
Lilly · Indianapolis, Indiana, United States of America · Principal
Function Therapeutic area Seniority Country
60%
Senior Principal Scientist, Analytical Sciences
Lilly · Watertown, Massachusetts, United States of America · Principal
Function Therapeutic area Seniority Country
60%
Sr. Principal or Engineering Advisor - Agentic Lab Automation Integration
Lilly · Indianapolis, Indiana, United States of America · Principal
Function Therapeutic area Seniority Country
60%
Principal Scientist, Downstream Process Development
Merck · Rahway, New Jersey, United States of America · Principal
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.