New · posted Oct 13
Genentech · Biotechnology
International Quality Lead
- South San Francisco, CA
- On-site
- Full-time
- Senior & Principal
Closes Nov 12, 2026 · 30 days left
The role
Are you ready to shape the future of quality management in healthcare? As a Quality Lead within our Pharma Development Quality (PDQ) division, you will support the Roche/Genentech organisation by developing and delivering robust Quality Assurance strategies, audits, and conclusions across molecules in development, post-approval products, and global processes. You will act as a trusted partner, ensuring our operations maintain the highest standards of compliance while directly influencing how we bring innovative therapies to patients safely and efficiently.
In this dynamic role, you will apply a risk-based approach to Quality Assurance using our Critical to Quality (CtQ) framework. By generating actionable data and insights through audits, you will collaborate closely with international stakeholders and play a vital part in preparing for and supporting regulatory authority inspections. This is an exceptional opportunity to utilise your expertise in a truly global, agile matrix environment where your insights drive continuous improvement.
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 Genentech / Roche!
What you need
You are a proactive, analytical quality professional who thrives on transforming complex data into clear, actionable solutions. You are an excellent communicator, highly skilled at collaborating across cultures and influencing stakeholders at various levels with or without formal authority. You look for opportunities to develop your skills within an international team and are passionate about continuous growth.
To be successful in this role, you bring:
- Education: A Bachelor’s degree or equivalent in a scientific or quality-related field, or equivalent combined experience.
- Industry Experience: Proven experience within the pharmaceutical, biotech, or medical device industry, with solid knowledge of end-to-end product operationalisation.
- GxP Knowledge: Strong exposure to and understanding of global GxP regulations and quality roles, specifically within GCP, GVP, or IVD/MD frameworks.
- Data & Digital Literacy: Excellent digital capabilities, with a good understanding of audit management and analytical reporting tools to drive data-led solutions.
- Critical Thinking: Proven problem-solving, decision-making, and project management skills with the ability to navigate ambiguous information.
Location
- This position is based at our South San Francisco, CA campus or Mississauga offices
- 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, CA is $111,000 - $206,100. 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.
What you'll do
- Drive Quality Strategies: Support the execution of risk-based Quality Assurance strategies and conclusions in predominantly Good Pharmacovigilance Practice (GVP) as well Good Clinical Practice (GCP),using the Critical to Quality (CtQ) framework.
- Lead Global Audits: Plan, perform, and lead audits, grouping individual issues into systematic trends to provide valuable quality data that fulfils regulatory requirements.
- Partner with Stakeholders: Establish and maintain strong partnerships with business stakeholders, presenting audit observations and associated compliance risks clearly.
- Support Inspections: Play a key role in regulatory authority inspection preparation and management.
- Advance PDQ Processes: Participate actively in assigned departmental goals and initiatives, contributing directly to the continuous improvement of PDQ processes.
- Maintain GxP Expertise: Maintain deep awareness and expertise in global regulations (such as FDA, EU, and ICH guidance) across GCP, GVP, or Medical Device frameworks.
Pay
$111,000 – $206,100 a year
Employer providedIf 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.
Where you'll work
South San Francisco, CAOn-siteOpen in Maps (opens in a new tab)
More jobs in South San Francisco, CAEqual opportunity, accessibility and legal noticesGenentech's statements, word for word
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.
Job intelligence
The context around this role
Live data · October 13, 2026
Salary intelligence
How the pay compares
This role's midpoint is 28% above the US median for Quality Assurance roles at this level.
This roleEmployer provided
Senior & Principal roles in California68 roles publishing pay
Senior & Principal roles in the US226 roles publishing pay
| Annual base pay | Low | Median | High |
|---|---|---|---|
| This role | $111,000 | — | $206,100 |
| California (middle half) | $123,000 | $135,750 | $159,750 |
| All US (middle half) | $105,625 | $124,000 | $140,875 |
This role: Genentech's own published range. Comparisons: the base pay employers published on open Quality Assurance roles at the same level on Regulatory Jobs, October 13, 2026. Nothing is estimated.
Career trajectory
Where this role sits in Quality Assurance
The general path across 642 open Quality Assurance roles on Regulatory Jobs, with the titles they carry most. Not Genentech's own promotion track.
Career resources on Quality Assurance
Skills DNA
What this role leans on
How many of the posting's 20 duty, requirement and summary lines touch each area. The posting's emphasis, not a proficiency score.
- GMP and compliance9
- Collaboration and leadership5
- Lab testing and methods2
- Quality systems and risk2
Regulatory intelligence
The rules behind this role
Frameworks and standards this posting's work falls under, matched from its own words, each linked to the official source.
Company hiring pulse
Genentech on Regulatory Jobs
- 20
- Open roles
- 20
- Distinct roles
- 5
- Locations
By discipline
- Quality13 65%
- Compliance & Safety4 20%
- Regulatory3 15%
By level
- Senior & Principal11 55%
- Associate & Specialist6 30%
- Director2 10%
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International Quality Lead at Genentech
Applications close November 12. $111K–$206K a year, employer provided.