New · posted Oct 19
Genentech · Biotechnology
Senior Quality Lead
- South San Francisco, CA
- On-site
- Full-time
- Senior & Principal
Open until filled
The role
We are seeking an experienced Senior Quality Lead to join the Quality Assurance Programs team. You will bring diverse thinking and technical experience in various Quality disciplines (e.g., GCP, CSV, device).
Note: This role requires strong level GCP knowledge and will be accountable for the quality assurance aspects and leading/supporting inspections of key molecules. CSV and device are preferred but not the main requirement.
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!
In Pharma Development Quality (PDQ), we strive for confidence in the integrity of our data and processes, agility, and unrivaled transparency with health authorities, patients, and society. Our work provides leadership, know-how, and partnering on quality across Molecules (GCP), Products (Drug and/or Medical Devices), Pharma affiliates, and global regulated processes.
This role supports the Roche/Genentech Organization by developing and delivering Quality Assurance strategies, audits, and conclusions for post approval products, affiliates and processes, based on a risk-based approach. Quality Assurance strategies are based on the Critical to Quality framework, encompassing Good Clinical Practice (GCP), Good Pharmacovigilance Practice (GVP), Medical Device, and Computer Systems (CS) requirements.
What you need
- Bachelor’s degree or equivalent in scientific or quality-related field. Advanced degree preferred.
- Demonstrated applied knowledge of clinical / pharmacovigilance / drug safety and regulatory requirements.
- Project management experience with proven leadership, mentoring and coaching; Demonstrated ability to effectively organize and execute tasks
- High degree of experience, competency, and proven track record leading multiple complex audit types in multiple GCP areas.
Preferrednice to have
- Device / CSV experience
- Strong digital and data literacy
- Experience hosting, managing and/or supporting regulatory authority inspections; Ability to formulate clear business questions that can be answered with data and utilize data/visualization tools to generate insights.
- Proven ability to influence and negotiate effective solutions, drive change, and assimilate new compliance information/trends.
- Proven record of working in a global, multicultural matrixed organization (multi-lingual skills desirable).
This role is based at our South San Francisco, CA campus. (Onsite presence is preferred, however, a remote option is a possibility.)
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 $141,000 - $261,800. 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 link provided below.
What you'll do
The Senior Quality Lead is a highly experienced Quality Professional who:
- Designs and delivers Quality Strategies and conclusions for assigned Molecules by applying a risk-based approach based on the Critical to Quality (CtQ) framework. Establish strong partnerships with business stakeholders and independently define the Quality Assurance approach, assessing specific risk areas and proposing strategy modifications.
- Define and Lead Audits: Define the audits required to deliver the Quality Assurance strategy and lead the development of methodology, including the use of data analytics.Independently perform and lead audits, managing preparation, conduct, presentation, timely reporting of outcomes, and evaluation of actions taken.
- Issue Management: Independently manage complex quality issues, group individual findings into systematic issues for process improvement, and escalate significant issues to PDQ management.
- Quality Conclusion and Stakeholder Communication: Independently draw conclusions on the Quality Positions and ensure appropriate action plans are developed to determine acceptability of evidence of compliance. Lead the presentation of observations and associated compliance risks to business stakeholders and Pharma representatives, including discussions with Legal and Regulatory Affairs.
- PDQ Goals and Initiatives: Contribute and participate in PDQ goals and initiatives to the execution and delivery of PDQ work and the development of PDQ processes.
- Health Authority Inspections:Lead and support regulatory authority inspections.
- Mentor and support the development of Quality Leads within the team.
- PDQ Leadership: Contribute to the long-term strategic direction of PDQ, lead departmental or cross-functional compliance projects, and lead the development/revision of PDQ processes and procedures (SOPs, Work Instructions).
- Expertise and Mentorship: Maintain expert knowledge of GCP/GVP regulations, company policies, and SOPs, assess the impact of new regulations, and act as a trainer and mentor for International and Senior Quality Leads.
- Networking: Maintain and influence partnerships with senior business stakeholders and PDQ domains. Facilitate cross-functional collaboration to ensure quality standards are met globally.
Pay
$141,000 – $261,800 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 20, 2026
Salary intelligence
How the pay compares
This role's midpoint is 67% above the US median for Quality Assurance roles at this level.
This roleEmployer provided
Senior & Principal roles in California89 roles publishing pay
Senior & Principal roles in the US302 roles publishing pay
| Annual base pay | Low | Median | High |
|---|---|---|---|
| This role | $141,000 | — | $261,800 |
| California (middle half) | $116,000 | $135,000 | $158,500 |
| All US (middle half) | $102,625 | $120,250 | $137,500 |
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 20, 2026. Nothing is estimated.
Career trajectory
Where this role sits in Quality Assurance
The general path across 895 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 28 duty, requirement and summary lines touch each area. The posting's emphasis, not a proficiency score.
- GMP and compliance12
- Collaboration and leadership12
- Documentation and SOPs4
- Regulatory submissions2
- Lab testing and methods1
- Quality systems and risk1
- Data and digital systems1
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.
From Regulatory News
Manufacturing and quality coverage for this professionCompany hiring pulse
Genentech on Regulatory Jobs
- 16
- Open roles
- 16
- Distinct roles
- 4
- Locations
By discipline
- Quality9 56%
- Compliance & Safety5 31%
- Regulatory2 13%
By level
- Senior & Principal12 75%
- Director2 13%
- Manager1 6%
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Senior Quality Lead at Genentech
Open until filled. $141K–$262K a year, employer provided.