Qureos Mentor

Genentech

<div><h3 class="jobSectionHeader">The Position</h3><h1 class="jobSectionHeader">
Technical Development Senior Scientist</h1>
The Pharma Technical Development (PTD) organization is responsible for translating scientific concepts into manufacturable products and ensuring a reliable supply of quality therapeutics to patients. PTD operates through collaboration and continuous process improvement to achieve its mission.
The Global Analytical Development and Quality Control (ADQC) function provides integrated analytical control strategies for the biologics pipeline. This includes developing, validating, and executing physico-chemical, immunochemical, and biological methods. ADQC's work directly supports CMC development, process development, product characterization, and drug delivery for biologics, spanning from early research (molecular assessment) through post-launch activities.
This position is based in South San Francisco, on site. 
The Opportunity
A Technical Development Senior Scientist position is available in Bioassay US within Genentech&rsquo;s PTD - ADQC. This is a critical hands-on position designed for an individual eager to develop deep expertise in cell engineering and molecular biology to advance our biotherapeutic pipeline.
You will be directly involved in the creation of next-generation cellular tools, enabling the generation mechanism-of-action (MOA) and characterization assays. This role provides an exceptional opportunity to work under the mentorship of a Technical Development Senior Principal Scientist, implementing cutting-edge technologies to drive the design and progression of novel assays.
If you are passionate about precision cell line engineering and thrive in a fast-paced, inclusive team environment, we encourage you to apply. 
Key Responsibilities
The successful candidate will be a core contributor to our cell engineering pipeline, focusing on the following areas:<ul><li>
You provide hands-on support for generating and maintaining mammalian cell lines required for functional assays and cell binding.</li><li>
Executing specialized molecular biology techniques, including vector design/cloning and production of viral vectors (i.e., lentiviral) to create reporter cell lines and stable expression cassettes.</li><li>
Applying CRISPR gene editing and other advanced cellular modification techniques to create precise cellular models for studying drug MOA.</li><li>
You perform quantitative analysis of engineered cell lines using techniques like FACS and PCR.</li><li>
Driving continuous improvement by incorporating current scientific and innovation trends, and collaborate cross-functionally to acquire necessary data to enable portfolio deliverables.</li><li>
You maintain meticulous laboratory records, contribute data to technical reports, present findings at internal group meetings, and represent our work at major external scientific conferences.</li></ul>
Who You Are (Required)<ul><li>
Ph.D. in a relevant field (e.g., Cell Biology, Molecular Biology, Bioengineering).</li><li>
Demonstrated proficiency in aseptic technique and maintaining cultures of a variety of mammalian cell types.</li><li>
Strong fundamental skills in molecular cloning, nucleic acid purification, and design principles for gene expression cassettes, reporters, and knockout strategies.</li><li>
Practical experience with nucleic acid delivery methods such as lipofection, nucleofection, and/or viral transduction (e.g., lentivirus).</li><li>
Experience with FACS-based methods for analyzing cell surface expression and/or functional reporters.</li><li>
Detail-oriented, highly organized, and demonstrated ability to manage and prioritize tasks for multiple projects concurrently.</li><li>
Strong oral and written communication skills suitable for documenting work and presenting data to the immediate team.</li></ul>
Relocation benefits are not available for this job posting.
The expected salary range for this position based on the primary location of California is 104,700.00 - 170,000.00 USD Annual. 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
Genentech 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.</div>

Technical Development Senior Scientist

<div><div><div>THE POSITION</div>
We advance science so that we all have more time with the people we love. A healthier future. It&rsquo;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&rsquo;s what makes us Roche.
Advances in AI, data, and computational sciences are transforming drug discovery and development. Roche&rsquo;s Research and Early Development organizations at Genentech (gRED) and Pharma (pRED) have demonstrated how these technologies accelerate R&amp;D, leveraging data and novel computational models to drive impact. Seamless data sharing and access to models across gRED and pRED are essential to maximizing these opportunities. The new Computational Sciences Center of Excellence (CoE) is a strategic, unified group whose goal is to harness this transformative power of data and Artificial Intelligence (AI) to assist our scientists in both pRED and gRED to deliver more innovative and transformative medicines for patients worldwide.
Within the CoE organization, the Data and Digital Catalyst (DDC) organization drives the modernization of our computational and data ecosystems and integration of digital technologies across Research and Early Development to enable our stakeholders, power data-driven science and accelerate decision-making.
The Engineering - AI Enablement group within DDC is accountable for&hellip; enabling AI! We do this across the board with our scientific and computational partners based on their goals. We help embed our AI strategy across our research organizations by providing employees with the tools and support needed to adopt AI into our daily work&mdash;helping us work smarter and enhancing our day-to-day work. We also build and deploy AI based solutions that reshape and transform business processes in order to unlock value at scale and optimize workflows. We also work on scaling up model training and inference, evaluating the quality of AI/ML models and output, and building impactful applications which accelerate the scientists doing the critical work of drug discovery and development. Partnering with colleagues to build, deploy and evolve a modern tech stack and utilities to enable our AI/ML and agentic efforts will be a key foundation to our success. Our aim is for everyone who can benefit from AI/ML to be able to leverage that utility where and when they need it, from data analysis to literature search to documentation writing. We are aiming for AI/ML to be an everyday utility. The team is cross-functional, impact driven, independent, and constantly evolving to meet the scientific needs.
The Opportunity:
As a software engineer in AI Enablement with a focus on backend and data engineering, you will be working closely with folks that span the gamut from Computational Scientists, Research Scientists, AI/ML experts, Product leaders, DevOps, and everyone in between. You'll build, own, and constantly improve scalable AI/ML based systems that unlock the potential of our diverse scientific data, accelerating the discovery and development of life-changing treatments for patients.<ul><li>
Design, develop, and test robust, scalable, and maintainable AI/ML facing scientific web applications and backend systems.</li><li>
Build tools to evaluate AI/ML model performance and establish new ways to understand AI quality.</li><li>
Partner with product managers and scientists to understand user needs, shape requirements, and translate them into actionable technical specifications.</li><li>
Develop and maintain systems for collecting, structuring, and storing diverse scientific data that support advanced analytics, machine learning, and other data-driven initiatives.</li><li>
Constantly improve the performance and effectiveness of our platforms, pipelines, and practices</li><li>
Contribute to architectural decisions, code reviews, and the evolution of our development processes.</li><li>
Be willing to span the stack and contribute where needed, even outside of your core area of expertise.</li><li>
Stay up-to-date with emerging technologies and industry best practices and adopt a culture of continuous learning, collaboration, and curiosity.</li></ul>
Who You Are:<ul><li>
Bachelor&rsquo;s, Master&rsquo;s or Ph.D. in Computer Science or similar technical field, or equivalent experience and 4+ years of professional experience in backend or data engineering roles (Senior Software Engineer) ; 7+ (Principal Software Engineer).</li><li>
Excellent proficiency with Python and backend languages such as Rust or Java</li><li>
Expert knowledge of ML performance optimization, GPU best practices.</li><li>
Experience with kubernetes, relational databases, NoSQL databases, or data lakes, and experience working on cloud-native architectures in public clouds (ideally AWS).</li><li>
Strong awareness of AI/ML frameworks, libraries, and toolsets.</li><li>
Proven understanding and application of engineering best practices.</li><li>
Excellent communication skills and ability to build trusted partnerships with internal and external collaborators.</li><li>
Ability to quickly acquire new technologies and programming languages and a passion for continuous learning.</li></ul>
Preferred But Not Required:<ul><li>
Experience with imaging or biological data and processes is a strong plus.</li><li>
Experience working with scientists or in a research environment is advantageous.</li><li>
Experience with workflow automation, GenAI, and/or agents is a plus.</li><li>
Experience with Rust is a massive plus.</li></ul>
This position requires onsite work 3 days per week.
The expected salary range for this position based on the primary location of San San Francisco, California $142,500-264,700 (Senior Software Engineer) and $162,600-302,000 (Principal Software Engineer). 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
#ComputationCoE
Relocation Benefits are available for this posting.
Genentech 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.</div>
<div><div>JOB FACTS
</div><div><div><ul><div>Job Sub Category
Research Informatics
</div><div>Schedule
Full time
</div><div>Job Type
Regular
</div><div>Posted Date
Dec 8th 2025
</div><div>Job ID
202512-131539</div></ul></div></div></div></div>

Senior/Principal Software Engineer, AI Enablement (Backend)

<div><div><div>THE POSITION</div>
2026 Summer Internship - External Quality
Department Summary
External Quality is responsible for the Quality and Compliance of externally sourced raw materials, supply from CDMOs, and distribution quality from Roche sites to Affiliates, including the certification for the EU market.<ul><li>
We serve our patients through external partnerships because access to quality products is every patient&rsquo;s right.</li><li>
We leverage external partners to offer flexibility to our internal capacity at the correct cost and quality.</li><li>
We enable our external partners to reliably deliver compliant, quality products to our supply chain customers so that we can deliver to patients worldwide.</li><li>
We do this through cross-functional collaborations, ensuring quality process excellence and continuous improvement.</li></ul> 
This internship position is located in South San Francisco, on-site.
The Opportunity<ul><li>
Provide quality and compliance oversight for external GxP suppliers, including CMO, CLO, suppliers or distributors of direct materials or critical process-contacting spare parts, suppliers for analytical equipment or manufacturing systems, and service providers to ensure compliance with cGMP and Quality Agreement requirements.</li><li>
Serve as the Quality Point of Contact (PoC) for designated suppliers and participate as a key member of GxP supplier cross-functional management teams to enable (as applicable for the supplier lifecycle stage) site selection and implementation (including due diligence activities), ongoing quality supply of commercial products, materials or services from suppliers, and decommissioning.</li><li>
Oversee all required quality activities during the lifecycle of a GxP supplier (Source &amp; Select, Implement, Manage, and Decommission), including but not limited to: process or method validations, Roche and Health Authority audits, complex investigations, market complaints, and regulatory submissions.</li><li>
Develop, negotiate and maintain risk-based Quality Agreements and Product Specific Requirements (as appropriate) with GxP suppliers and ensure compliance with agreements.</li><li>
Collaborate with GxP suppliers to address gaps of audit responsiveness, CAPA implementation, deviation reporting and management, complaint management, investigation closure, and change implementation with regard to quality and time with the supplier; and escalate as appropriate.</li><li>
As applicable, manage all required activities to support Make Assess Release (MAR) of commercial medicinal products including approval of master process documentation, resolution of investigations, assessment of changes, and monitor and report GxP Supplier quality performance.</li><li>
As applicable, release, reject or quarantine commercial medicinal products (drug substance or API, bulk drug product, and semi-finished and finished products) and medical devices produced within the area of responsibility per applicable Swissmedic and Roche requirements on behalf of the Responsible Person (RP).</li><li>
As applicable, collaborate with GxP suppliers to maintain the manufacturing processes and the Specifications and Analytical Methods (SAM) in a validated state and compliant with the regulatory dossier, including stability testing programs.</li><li>
As applicable, develop and maintain quality risk management plans; utilize risk management tools to identify and mitigate supplier quality and compliance risks, ensuring suppliers are in a state of continuous inspection readiness.</li><li>
As applicable, manage or lead technical transfers for manufacturing, testing, packaging, and product launches.</li><li>
As applicable, support or lead supplier improvement initiatives to solve complex manufacturing or quality problems. Identify, design and implement process and system improvements.</li></ul>
Program Highlights<ul><li>
Intensive 12 months, full-time (40 hours per week) paid internship.</li><li>
Program start dates are in June 2026 (Summer).</li><li>
A stipend, based on location, will be provided to help alleviate costs associated with the internship.</li><li>
Ownership of challenging and impactful business-critical projects.</li><li>
Work with some of the most talented people in the biotechnology industry.</li></ul>
Who You Are (Required)
Required Education - You meet one of the following criteria:<ul><li>
Must have attained a Bachelor's degree (recent graduates not currently enrolled in a grad program).</li><li>
Have attained a Master's Degree.</li><li>
Have attained a PhD.</li></ul>
Required Majors: Biotechnology, Bioengineering, Chemistry, Biochemistry, Biology.
Required Skills:<ul><li>
Knowledge of cGMP, ISO standards and international regulations for pharmaceuticals.</li><li>
Ability to interpret quality standards as they relate to GxP suppliers.</li><li>
Highly competent in MS Office or Google Suite applications including Excel, PowerPoint, Word, and MS Project, etc.</li><li>
Ability to communicate clearly and professionally both in writing and verbally.</li><li>
Fluency in oral and written English is a must.</li></ul>
Preferred Knowledge, Skills, and Qualifications:<ul><li>
Previous experience in the pharmaceutical or related industry or an equivalent combination of education and experience is a plus.</li><li>
Experience with GxP suppliers such as CMO, CLO, and direct material suppliers is a plus.</li><li>
Operational Excellence expertise is a plus.</li><li>
Additional language skills are a plus.</li><li>
Excellent communication, collaboration, and interpersonal skills.</li><li>
Complements our culture and the standards that guide our daily behavior &amp; decisions: Integrity, Courage, and Passion.</li></ul> 
Relocation benefits are not available for this job posting.
The expected salary range for this position based on the primary location of South San Francisco is $33.00-$46.00 per hour. Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law. This position also qualifies for paid holiday time off benefits.
Genentech 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.</div>
<div><div>JOB FACTS
</div><div><div><ul><div>Job Sub Category
Internships &amp; Co-ops
</div><div>Schedule
Full time
</div><div>Job Type
Temporary (Fixed Term)
</div><div>Posted Date
Dec 5th 2025
</div><div>Job ID
202512-131177</div></ul></div></div></div></div>

2026 Summer Internship - External Quality

<div><div><div>THE POSITION</div>
2026 Summer Intern - Global Procurement
Department Summary
Global Procurement - (PT Procurement Network) is responsible for maximizing the value delivered to Roche &amp; Genentech's Drug Substance and Drug Product portfolio of cGMP direct material goods and services. Direct Materials are those raw materials from suppliers that directly impact our drug products (e.g. vials, stoppers, filters, chemicals, resins, etc). 
 
The intern will support Global Category Managers in leading cross-functional teams to develop and implement optimal total-cost-of-ownership solutions that address supply chain, operations, technical, and quality business requirements. The intern will develop and implement projects internally (within Roche) and externally (with suppliers) for operational optimization, quality improvement, global network alignment, and cost savings initiatives.
This internship position is located in South San Francisco, on-site.
The Opportunity<ul><li>
Understanding of Direct Materials Supplier Management at Roche.</li><li>
Technical understanding of direct material impact on the biotech business, product, cGMP practices and Quality systems.</li><li>
Project management skills as project lead and participant.</li><li>
Relationship management, facilitation and influencing skills of cross-functional teams.</li><li>
Operational/tactical procurement activities including spend analysis, cost savings project management, performance metric trending, and beyond.</li></ul>
Program Highlights<ul><li>
Intensive 12 months, full-time (40 hours per week) paid internship.</li><li>
Program start dates are in May/June (Summer).</li><li>
A stipend, based on location, will be provided to help alleviate costs associated with the internship.</li><li>
Ownership of challenging and impactful business-critical projects.</li><li>
Work with some of the most talented people in the biotechnology industry.</li></ul>
Who You Are
Required Education:<ul><li>
Must have attained a Bachelor's Degree (not currently enrolled in a graduate program).</li><li>
Targeting 2024 graduates and students graduating in 2025.</li></ul>
Required majors:
<ul><li>Science background, engineering, operations management, or finance with a science minor.</li></ul>
Required skills:
<ul><li>Strong communication, leadership/collaboration, and project management skills.</li><li>
Ability to operate and execute effectively in a dynamic, fast-paced environment with multiple priorities and challenging deadlines.</li><li>
Self-starter with an agile mindset &amp; hands-on mentality who navigates and takes advantage of ambiguity to seek the most effective and sustainable outcomes.</li><li>
Process-oriented with strong analytical skills, strategic thinking, and creative problem-solving capabilities.</li><li>
Demonstrates a sense of urgency and proactive approach that is focused on results.</li></ul>
Preferred Knowledge, Skills, and Qualifications:<ul><li>
Advanced in all Google Suite tools and Tableau tools.</li><li>
Excellent communication, collaboration, and interpersonal skills.</li><li>
Complements our culture and the standards that guide our daily behavior &amp; decisions: Integrity, Courage, and Passion.</li><li>
Highly effective at building internal and external relationships.</li></ul>
Relocation benefits are not available for this job posting.
The expected salary for this position based on the primary location of California is $33.00 per hour. Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law. This position also qualifies for paid holiday time off benefits.
Genentech 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.</div>
<div><div>JOB FACTS
</div><div><div><ul><div>Job Sub Category
Internships &amp; Co-ops
</div><div>Schedule
Full time
</div><div>Job Type
Temporary (Fixed Term)
</div><div>Posted Date
Dec 5th 2025
</div><div>Job ID
202512-131386</div></ul></div></div></div></div>

2026 Summer Intern - Global Procurement

Join Genentech and explore 4   exciting career opportunities. They're hiring for various roles with options for remote or on-site work. Apply today and become part of their innovative team.

Genentech

ABOUT_COMPANY

Technical Development Senior Scientist

Senior/Principal Software Engineer, AI Enablement (Backend)

2026 Summer Internship - External Quality

2026 Summer Intern - Global Procurement