2,703 Results for

Quality Director Jobs in Redwood City, CA

Jobs

New!

Santa Clara, CA4 days ago

$225,000–$300,000 Per Year

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New!

Pleasanton, CA1 day ago

$2,337–$2,337

Advantis Medical, the #1 rated travel nurse agency, is currently seeking an experienced Director of Nursing Registered Nurse (RN) for an exciting new travel job in Pleasanton, CA 94588. If you are an experienced Director of Nursing Registered Nurse (RN) with a passion for providing exceptional patient care, just let us know you’re interested.

New!

Palo Alto, CA1 day ago

$1,956–$1,956

Advantis Medical, the #1 rated travel nurse agency, is currently seeking an experienced Director of Nursing Registered Nurse (RN) for an exciting new travel job in Palo Alto, CA 94303. If you are an experienced Director of Nursing Registered Nurse (RN) with a passion for providing exceptional patient care, just let us know you’re interested.

New!

San Jose, CAToday

$26.80–$32.20

When you join our team as a Site Director, you will: Lead and supervise a group of teachers to create unique and engaging classroom experiences, leverage and develop “best in class” educators to be passionate and committed professionals. At KinderCare Learning Companies, the first and only early childhood education provider recognized with theGallup Exceptional Workplace Award, we offer a variety of early education and child care options for families.

New!

Sunnyvale, CAToday

$16.35–$33.15

New!

Cupertino, CAToday

$16.35–$33.15

New!

Cupertino, CAToday

$16.35–$33.15

New!

Daly City, CAToday

$24.65–$34.55

New!

Cupertino, CAToday

$16.35–$33.15

New!

Emeryville, CA1 day ago

Ensure practice is appropriately represented and demonstrates their value through leadership roles (as applicable) and/or participation with hospital management, medical staff leadership, Medical Executive, Medical Staff and other hospital committees, and within the local community. Strategize and execute a comprehensive annual practice management plan that sets clear goals and objectives, continuously surpassing expectations and delivering value to patients, clients, providers, and the local community.

New!

Redwood City, CA1 day ago

New!

Burlingame, CA1 day ago

Sutter Mills-Peninsula Medical Center earned five stars, the highest ranking possible, in the CMS Overall Hospital Quality Star Ratings and an Outstanding Patient Experience Award, placing it among the top 15 percent of hospitals in patient experience. Ensure practice is appropriately represented and demonstrates their value through leadership roles (as applicable) and/or participation with hospital management, medical staff leadership, Medical Executive, Medical Staff and other hospital committees, and within the local community.

San Jose, CA18 days ago

$145–$159 Per Hour
Full-time

We are seeking an experienced hospitalist with leadership capabilities for Regional Medical Center, a thriving hospitalist program located in the heart of tech mecca, San Jose, California. Competitive Compensation, with an estimated base salary range of $145 to $159 hourly, RVU and quality bonus, plus leadership stipend, with the opportunity to earn additional incentives.

New!

Emeryville, CA1 day ago

Commit to creating and demonstrating inclusivity within Vituity including codesigning, building, and executing strategies, policies, and practices that cultivate equity, inclusion, and fair opportunity for all; demonstrating preparedness to educate, mitigate, coach, and address daily bias and exclusion in partnership with the site leadership. Accountable for ensuring meaningful integration occurs: Identify opportunities for practice line integration to ensure the quality and efficiency of patient care delivery across the acute care continuum; assist with new service line startups; engage regularly with integrated site RDs.

San Jose, CA13 days ago

$139,256–$222,768

Our infrastructure includes a fullyautomated esoteric core laboratory in Fort Lauderdale, a histology and microbiology operation in Largo,Florida, and a network of hospital based rapid-response laboratories present in fourHCA Healthcare divisions within the state of Florida. Additional options for dental and vision benefits, life and disability coverage, flexible spending accounts, supplemental health protection plans (accident, critical illness, hospital indemnity), auto and home insurance, identity theft protection, legal counseling, long-term care coverage, moving assistance, pet insurance and more.

san jose, CA30+ days ago

$140,000–$165,000 Per Year

Oversight of managing and improving site supplier quality Be an advocate for lean and six sigma manufacturing principles and drive continuous improvement Drive cross functional projects with manufacturing, supply chain, and engineering to verify and validate existing manufacturing processes and capabilities Coordinate development of Quality Plan and participate in Design for Manufacturability (DFM) reviews for new customer on-boarding Address process yields by driving cross-functional teams to develop and implement corrective actions utilizing a methodical approach (DMAIC) to root cause and continuous improvement. Recognized as a technology leader, Sanmina Corporation provides end-to-end manufacturing solutions, delivering superior quality and support to Original Equipment Manufacturers (OEMs) primarily in the communications networks, defense and aerospace, industrial and semiconductor systems, medical, multimedia, computing and storage, automotive and clean technology sectors.

San Leandro, CA23 days ago

$116,000–$147,000 Per Year

Kindred Hospital San Francisco Bay Area is a 99-bed long-term acute care hospital offering the same in-depth care you would receive in a traditional hospital, but for an extended recovery period. Maintains oversight responsibility for all regulatory body surveys, including The Joint Commission (TJC), State Licensing Reviews, and CMS Validation surveys.

Pleasanton, CA30+ days ago

10+ years of relevant regulatory affairs experience in the bioanalytical CRO or biotechnology/pharmaceutical industry, or a combination of education and experience. Crystal Bio Solutions, a member of Crystal Pharmatech, is a leading biologics analytical organization with operations in the San Francisco Bay Area and New Jersey.

Santa Clara, CA30+ days ago

This is a high-impact technical leadership role perfect for a hands-on seasoned QE leader who has experience running large quality engineering and tool development organizations. Oversee the long term testing / pre-production environment strategy, ensuring high availability and stability for testing environments used by the entire company.

San Francisco, CA30+ days ago

$192,000–$210,000 Per Year

Data and Metrics Governance • Understand and support existing key performance indicators (KPIs) and quality metrics to ensure process improvements align with organizational objectives • Assess impact of proposed system and data changes on established governance frameworks and data integrity • Collaborate with data governance teams to evaluate risks and opportunities related to metrics and reporting when implementing process changes • Analyze performance data to identify trends, opportunities, and areas for improvement while maintaining alignment with existing measurement systems. • Model: Operational Excellence Focus • Location: San Francisco Bay Area preferred; other northern California locations considered • Success Metrics • Successful implementation of quality improvement initiatives • Measurable improvements in operational KPIs and process efficiency • Effective stakeholder engagement and cross-functional collaboration • Timely completion of assigned projects and deliverables • Knowledge transfer and capability building within client organization.

New!

Alameda, CA6 days ago

$190,000–$269,000 Per Year

Acts as the Subject Matter Expert for current global regulatory compliance expectations and proactively reviews changes in regulatory requirements and industry environment that would necessitate future changes and drives completion of impact assessments. Responsible for setting the strategic plan for maintaining organizational inspection readiness across the organization and developing an annual inspection readiness plan, ensures activities are completed, and drives continuous improvement initiatives.

San Jose, California30+ days ago

$190,000–$230,000 Per Year

Driven by a belief that infectious disease diagnosis should be quick, accurate, and accessible to all, Visby has developed the world’s first single-use PCR platform that disrupts the traditional model and redefines the way infectious disease is tested and treated.$190,000 You will lead and participate in all aspects of the quality management system (QMS) and work closely with cross-functional teams to drive continuous improvement and maintain compliance with the QMS throughout the product lifecycle.

Sunnyvale, CA17 days ago

$200,000–$230,000 Per Year

A Director of Quality Management who excels in this role: Provides leadership and oversight of a comprehensive, efficient and integrated organization wide Continuous Quality Performance Improvement program. We are part of Lifepoint Health, a diversified healthcare delivery network committed to making communities healthier with acute care, rehabilitation, and behavioral health facilities from coast to coast.

South San Francisco, CA30+ days ago

$193,000–$242,000 Per Year

The Clinical QA Director is responsible to ensure quality is embedded throughout the lifecycle of all the ongoing clinical programs through oversight, assessment and monitoring, risk assessment tools, auditing and risk mitigations. This involves working closely with Clinical Operations, Clinical Development, Clinical Supply Chain, Data Management, Pharmacovigilance, Medical Affairs, Regulatory, Legal, and other teams across Alumis.

Alameda, California30+ days ago

$210,000–$250,000 Per Year

GeneFab's technology platform includes bioinformatic-guided discovery of cell type promoters, directed evolution of small molecule-regulated gene switches, and the engineering of highly sensitive kill switches for enhanced safety and control of cellular therapies. A minimum of 15 years of experience in compliance, quality, and CDMO/CMO management with a focus on regulatory documentation and lifecycle management within the pharmaceutical or biotechnology industry is a must, including 10 years of experience in management/leadership roles.

San Francisco, CA30+ days ago

Lead brand-level fit strategy in close partnership with Design to ensure aesthetic intent is executed with precision, leveraging customer feedback, return insights, and body data to deliver consistent, customer-centric fit across categories and sizes. Partner with Product Development and Sourcing to drive vendor readiness and capability across fit, quality, and product integrity, while advancing cost engineering to deliver optimal cost, trend-right product, and margin alignment.

New!

Palo Alto, California4 days ago

HARMONi: Phase 3 clinical study which was intended to evaluate ivonescimab combined with chemotherapy compared to placebo plus chemotherapy in patients with EGFR-mutated, locally advanced or metastatic non-squamous NSCLC who were previously treated with a 3rd generation EGFR TKI. The Senior Director QA will report to the Vice President, Quality Assurance and Regulatory CMC, and provide comprehensive GMP quality oversight across the full chemistry, manufacturing, and controls (CMC) lifecycle for Summit’s oncology pipeline.

South San Francisco, CA30+ days ago

$205,000–$218,000 Per Year

We work hard to bring together diverse teams-grounded in a wide range of expertise and life experiences-and work even harder to ensure those teams thrive in inclusive, growth-oriented environments supported by equitable company and team practices. These powerful models rely on extensive biological and computational infrastructure and allow insitro to advance novel targets and patient biomarkers, design therapeutics and inform clinical strategy.

South San Francisco, CA30+ days ago

$193,638–$224,270 Per Year

The Associate Director, GCP Clinical Quality will play a key role in ensuring the successful execution of Denali's clinical trials by delivering strategic quality oversight and fostering a culture of compliance and continuous improvement. Key Accountabilities/Core Job Responsibilities: Serve as a GCP Quality team member on Study Execution Teams (SETs) and deliver a cohesive strategic GCP framework across Denali clinical trials.

South San Francisco, CA30+ days ago

$184,500–$215,250 Per Year

This role will hare strategic responsibility for the QA CSV / CSA function to support cross-functional and QA goals for GXP systems and deliver results for corporate initiatives, as well as independently drive and own multiple complex CSV-related projects in partnership with multiple cross-functional leaders. Cytokinetics is a specialty cardiovascular biopharmaceutical company, building on its over 25 years of pioneering scientific innovations in muscle biology, and advancing a pipeline of potential new medicines for patients suffering from diseases of cardiac muscle dysfunction.

Redwood City, CA30+ days ago

Lead, manage, and train others on GCP audits, including clinical investigative site audits, clinical vendor audits, clinical department internal audits, Trial Master File (TMF) audits, and applicable study document audits, including Clinical Study Reports (CSRs). The Director of Clinical Quality Assurance (CQA) is a senior member of the CQA team and will lead and perform day-to-day clinical quality operations and compliance activities to support the success of the clinical studies sponsored or supported by Corcept.

San Jose, California28 days ago

Lyten is leading an industrial revolution through Lyten 3D Graphene, a breakthrough supermaterial unlocking a new generation of products — from lithium–sulfur batteries and energy storage systems to concrete admixtures, lightweight composites, and next-generation sensors that are revolutionizing industries. Doctorate degree in engineering or general sciences AND 12+ years of experience in Quality OR Master's degree in engineering or general sciences AND 14+ years of experience in Quality OR Bachelor's degree in engineering or general sciences AND 16+ years of experience in Quality OR equivalent experience.

New!

Foster City, California4 days ago

Provide quality oversite for the GCP/GVP/GLP vendor activities, including internal/external deviations, CAPAs, change controls, and KPIs/KQIs. 10-12 years of experience in the pharmaceutical industry, including 5-10 years in GCP Quality and 5+ years supervising GCP Quality internal staff and/or external consultants.

South San Francisco, CA30+ days ago

$232,000–$271,000 Per Year

The Associate Director, Analytical Development and Quality Control will report to the Director & Head of Analytical Development and Quality Control and will be responsible for providing and executing analytical development strategy for small-molecule candidates from early development through late stage, including analytical method development, validation, and transfer; stability programs; and phase-appropriate specifications and analytical control strategies for drug substance (DS), drug product (DP), and related critical materials. Demonstrated track record of managing CROs and CDMOs, preferably on both analytical and bioanalytical projects, in developing methods and quality control strategy for testing of small-molecule drug candidates supporting Phase I to commercial launch.

South San Francisco, CA30+ days ago

$230,000–$270,000 Per Year

Led by a management team with significant experience in cell therapy, Allogene is developing a pipeline of "off-the-shelf" CAR T cell product candidates with the goal of delivering readily available cell therapy on-demand, more reliably, and at greater scale to more patients. About Allogene: Allogene Therapeutics, with headquarters in South San Francisco, is a clinical-stage biotechnology company pioneering the development of allogeneic chimeric antigen receptor T cell (AlloCAR T) products for cancer and autoimmune disease.

Walnut Creek, CA7 days ago

$200,000–$250,000 Per Year

This role plays a critical leadership position in defining and scaling Kinder's quality systems, ensuring that every product delivered to market is safe, compliant, and consistently exceptional in taste and performance. Most of our work happens in the office to spark creativity and community, but we also offer flexibility so team members have the autonomy to work outside the office when needed to support their work-life balance and personal commitments.

San Jose, CA26 days ago

$170,700–$256,100 Per Year

Lyten is leading an industrial revolution through Lyten 3D Graphene, a breakthrough supermaterial unlocking a new generation of products - from lithium-sulfur batteries and energy storage systems to concrete admixtures, lightweight composites, and next-generation sensors that are revolutionizing industries. Doctorate degree in engineering or general sciences AND 12+ years of experience in Quality OR Master's degree in engineering or general sciences AND 14+ years of experience in Quality OR Bachelor's degree in engineering or general sciences AND 16+ years of experience in Quality OR equivalent experience.

Sunnyvale, CA30+ days ago

$115,900–$141,700 Per Year

As a Director of Quality Management, your responsibilities will include: Initiate and manage key projects for product quality improvement, such as reducing cost of quality, product RMA rate and IQC failure rate, increasing production yield rate etc…; closely drive and track them to completion with all targets achieved. Strong people management experience and skill to assess and utilize existing team's skill sets and capabilities to support business needs, and to hire, coach, mentor new team members for business expansion.

Foster City, CA30+ days ago

$190,000–$205,000 Per Year

10-12 years of experience in the pharmaceutical industry, including 5-10 years in GCP Quality and 5+ years supervising GCP Quality internal staff and/or external consultants. Provide quality oversight for the GCP/GVP/GLP vendor activities, including internal/external deviations, CAPAs, change controls, and KPIs/KQIs.

San Jose, CA20 days ago

Oversee the harmonization of quality system processes at various global sites included in the scope of the Invisalign quality system including internal audits, document control, risk management, non-conformance and corrective action handling, inspections, training, and management review. The successful candidate will partner with Align Global QMS leaders to create a quality management infrastructure that is compliant, effective, efficient, agile, and that supports a rapidly growing business with complex and diverse product lines (both hardware and software).

Menlo Park, CA17 days ago

$213,000–$240,000 Per Year

Role Overview: The Director, Quality Control - Combination Products will provide strategic and operational leadership for the Quality Control function supporting late-stage clinical development, analytical testing oversight for clinical drug substance and drug product, process performance qualification (PPQ), regulatory submissions, and commercial launch readiness for monoclonal antibody drug products and combination products, including pre-filled syringes and autoinjectors. Strong knowledge of cGMP regulations and global regulatory expectations, including 21 CFR Parts 210, 211, and 4. Hands-on experience supporting combination products such as pre-filled syringes, autoinjectors, or related delivery systems.

New!

South San Francisco, CA6 days ago

$215,600–$266,300 Per Year

The Director, CMC QA will report to the Senior Director of CMC QA and be responsible for maintaining strategic responsibility over QA Manufacturing Operations, developing and implementing Ultragenyx CMC Quality approach for assigned programs, and working with colleagues to improve processes utilized to ensure product quality. In this role, in collaboration with key stakeholders in Technical Operations, DIR CMC QA provides quality oversight and support to ensure clinical through commercial development lifecycle activities for drug substance and drug product meet cGMP regulatory requirements and guidelines.

Berkeley, CA7 days ago

$220,000–$235,000 Per Year

Provide Clinical Quality Assurance (GCP) strategic and technical leadership and Subject Matter Expertise (SME) to clinical study teams; Partner with the teams to effect appropriate and timely documentation of quality event management, including CAPA plans in support of product pipeline. The successful candidate must have the ability to execute QA tasks independently; effectively represent QA in a GCP, PV, and GLP focused team settings and manage quality related activities related to clinical vendors, investigator sites and regulatory agencies.

Menlo Park, CA17 days ago

$213,000–$240,000 Per Year

Review and approve GMP documentation, including master batch records, executed batch records, analytical methods, specifications, validation protocols and reports, tech transfer documentation, stability protocols and reports, and risk-assessment documentation. Oruka's mission is to offer patients suffering from chronic skin diseases like plaque psoriasis the greatest possible freedom from their condition by achieving high rates of complete disease clearance with dosing as infrequently as once or twice per year.

San Francisco, CA30+ days ago

$226,100–$266,000 Per Year

This is a newly created role designed to establish and lead Oura's Core Technology Quality function a group of deep subject matter experts (SMEs) embedded within the Quality organization to provide specialized technical depth across the most complex electrical domains in our products. Lead FA/CA for Core Technology domains: Lead comprehensive Failure Analysis (FA) on battery, PWBA, EE component, and EE module failures; drive root cause identification and implement robust Corrective Actions (CA) through Design of Experiments (DOEs) and Product Release Qualifications (PRQs).

New!

San Francisco, CAToday

The Director supports both fee for service and cost reimbursed programs across multiple counties and service lines to promote a culture of accountability and with a focus on practical implementation, regulatory excellence, risk mitigation, and continuous quality improvement. Employees are expected to exercise sound judgment, remain aware of their surroundings, follow established safety, communication, and de-escalation procedures, participate in all required trainings, and promptly report incidents, threats, injuries, or unsafe conditions, in accordance with ECS policies and procedures.

San Francisco, CA30+ days ago

Lead brand-level fit strategy in close partnership with Design to ensure aesthetic intent is executed with precision, leveraging customer feedback, return insights, and body data to deliver consistent, customer-centric fit across categories and sizes. This leader reports to the Vice President, Technical Design & Quality, Gap Inc. and balances strategic leadership with deep operational execution, translating enterprise vision into measurable brand outcomes while driving day-to-day excellence.

Santa Clara, CA30+ days ago

Act as the voice of the customer, addressing complaints, ensuring needs are met, and be the key contact point for supporting complex and high impact quality-related issues with potential for considerable impact to the business. We are looking for a Senior Director of Customer Quality Engineer in a leadership role to support lead our customer quality assurance activities, stationed in Santa Clara, California!

Brisbane, CA30+ days ago

$170,538–$193,493 Per Year

As a virtual drug developer, Nurix operates through a lean internal infrastructure and relies on a curated ecosystem of Software-as-a-Service (SaaS) and cloud-hosted platforms to support GxP-regulated activities across clinical development, quality operations, manufacturing oversight, and regulatory submissions. The role requires an individual who combines deep technical knowledge of GxP computerized systems with practical experience in SaaS and cloud-based platform qualification, and who can translate regulatory requirements into pragmatic, fit-for-purpose validation approaches that support a modern, agile biotech environment.

Silicon Valley, CA30+ days ago

As a Director, you drive business growth by overseeing multiple projects, cultivating executive-level client relations, and mentoring the future leaders. Examples of the skills, knowledge, and experiences you need to lead and deliver value at this level include but are not limited to: • Lead in line with our values and brand.

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Quality Director Jobs in Redwood City, CA

Tax Director Jobot

Travel Nurse RN - Director of Nursing - $2,337 per week in Pleasanton, CA TravelNurseSource

Travel Nurse RN - Director of Nursing - $1,956 per week in Palo Alto, CA TravelNurseSource

Site Director at Miller Middle School KinderCare Education

Site Director at Cupertino Middle School KinderCare Education

Site Director at Garden Gate Elementary School KinderCare Education

Site Director at Faria Elementary School KinderCare Education

Site Director at Benjamin Franklin Intermediate KinderCare Education

Site Director at Collins Elementary School KinderCare Education

Medical Director Ambassador - Hospital Medicine - Traveling - Nationwide Vituity

Medical Director Correctional Health - San Mateo County Jail Vituity

Medical Director - Psychiatry - Mills-Peninsula Medical Center Vituity

Hospitalist Assistant Medical Director in San Jose, CA TeamHealth

Regional Director - Anesthesiology - Vituity Practice Management - Emeryville Vituity

Hospital Laboratory Director Good Samaritan Hospital

Regional Director of Quality Engineering Sanmina Corp

Director of Quality Management Full Time Knight Health Holdings LLC

Manager/ Director of Quality Assurance CRYSTAL PHARMATECH INC

Director of Quality Engineering Netskope Inc

Senior Director of Quality Assurance Jones Lang LaSalle Inc

Compliance QA Director Exelixis Inc

Director of Quality Visby Medical

Director of Quality Management (DQM) LifePoint Health Inc

Director, Clinical Quality Assurance - Contractor Alumis Inc

Director of Quality Assurance GeneFab

Senior Director, Technical Design & Quality The Gap Inc

Senior Director of Technical QA (GMP) Summit Therapeutics

Director, Quality Assurance Insitro Inc

Associate Director, Clinical Quality Denali Therapeutics Inc

Associate Director, QA Computer System Validation Cytokinetics Inc

Director, Clinical Quality Assurance Corcept Therapeutics Inc

Sr Director, Quality Lyten

Associate Director, GCP QA Mirum Pharmaceuticals

Associate Director, Analytical Development and Quality Control Aligos Therapeutics Inc

Senior Director, Validation and Quality Engineering Allogene Therapeutics Inc

Sr. Director, Food Safety & Quality Assurance Kinder's

Sr Director, Quality Lyten Inc

Director, Quality Management Fortinet Inc

Associate Director, GCP QA Mirum Pharmaceuticals Inc

Director, Quality Systems Align Technology, Inc.

Director, Quality Control Oruka Therapeutics Inc

Director External Quality Assurance Ultragenyx Pharmaceutical Inc

Director of Quality Assurance, Clinical Caribou Biosciences, Inc.

Director, GMP Quality Assurance Oruka Therapeutics Inc

Director, Electrical Modules Quality Ouraring Inc

Quality Management Director Episcopal Community Services

Sr Director, Technical Design & Quality - Old Navy The Gap Inc

Senior Director, Customer Quality Engineering NVIDIA Corp

Associate Director, Computer Systems Assurance Quality Nurix Therapeutics Inc

Payer Quality Consultant, Director PricewaterhouseCoopers LLP

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