Top 287 Quality manager Jobs in San Mateo, Ca

Manager, Quality Assurance
THINK Surgical, Inc. —Fremont, CA
- $165,000 - $180,000 a year
- Weekends as needed
- Engineering
- Office
- 3 years
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Quality Manager
Westfall Technik —Union City, CA
- $130,000 - $140,000 a year
- Full-time
- 5 years
- Engineering
- Senior level
- Paid parental leave
- AD&D insurance
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6d
Quality Assurance Manager, Home
Quince —San Francisco, CA
- $130,000 - $155,000 a year
- Background check
- Team management
- Senior level
Senior Quality Operations Manager
Retro —Redwood City, CA
- $175,000 - $190,000 a year
- Full-time
- 6 years
- Training & development
- Senior level
- Paid parental leave
- Paid holidays
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Manager, Clinical Quality
iRhythm Technologies, Inc. —San Francisco, CA
- $115,000 - $149,000 a year
- Full-time
- Hybrid work
- Microsoft Word
- Microsoft Excel
- Microsoft Outlook
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Director of Quality Assurance
Vital Connect Inc —San Jose, CA
- $200,000 - $230,000 a year
- Management
- 8 years
- Bachelor's degree
- Dental insurance
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Quality Control Manager
Joby Aviation —San Carlos, CA
- $95,600 - $195,000 a year
- Full-time
- Writing skills
- 3 years
- Master's degree
- Employee stock purchase plan
- Disability insurance
5d
Senior Manager, Quality Systems - Lingo (on-site)
Abbott Laboratories —Alameda, CA
- $130,700 - $261,300 a year
- Full-time
- 7 years
- Bachelor's degree
- Recruiting
- Health insurance
- Tuition reimbursement
Manager, Quality Assurance
Triple Ring Technologies —Newark, CA
- $125,000 - $150,000 a year
- Hybrid work
- Bachelor of Science
- Bachelor's degree
- Software development
- Paid holidays
- Health insurance
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Supervisor, Quality Inspector (Day Shift)
Tesla —Fremont, CA
- $96,000 - $168,000 a year
- Full-time
- Mid-level
- Mentoring
- Communication skills
- Commuter assistance
- Health savings account
Quality Engineering Manager
Unigen —Newark, CA
- $130,000 - $150,000 a year
- Full-time
- Engineering
- 3 years
- Senior level
- 401(k) matching
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Senior Manager, Quality Assurance Program
Rigel Pharmaceuticals, Inc. —South San Francisco, CA
- $140,000 - $170,000 a year
- Full-time
- Hybrid work
- 6 years
- Travel
- Senior level
- Paid holidays
- Disability insurance
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Quality Engineering, Manager
Joby Aviation —San Carlos, CA
- $170,500 - $267,400 a year
- Full-time
- 3 years
- Bachelor's degree
- Doctor of Philosophy
- Employee stock purchase plan
- Disability insurance
Senior Manager Quality Assurance
Safeway —San Leandro, CA
- $130,000 - $160,000 a year
- Full-time
- 5 years
- Office
- Analysis skills
- Paid holidays
- Disability insurance
Quick Apply
Manager, Quality & Safety
Fictiv —Oakland, CA
- $125,000 - $140,000 a year
- Remote
- Bachelor of Science
- Engineering
- Travel
- Health insurance
- Dental insurance
Quick Apply
QA Manager, Training Services
Penumbra —Alameda, CA
- $137,000 - $194,000 a year
- 5 years
- Office
- Bachelor's degree
- Paid parental leave
- AD&D insurance
Document Control Manager
Rani Therapeutics —Fremont, CA
- $139,409 - $190,000 a year
- 5 years
- Computer literacy
- Organizational skills
Quick Apply
Quality Assurance Supervisor
Reyes Coca-Cola Bottling —San Leandro, CA
- $88,816 - $111,020 a year
- Full-time
- Management
- Mid-level
- High school diploma or GED
- Health insurance
- Dental insurance
Quick Apply
Senior Manager, Quality Assurance (GMP Operations)
Gilead Sciences —Foster City, CA
- $157,590 - $203,940 a year
- Full-time
- Bachelor of Science
- Analysis skills
- Bachelor's degree
- Health insurance
- Dental insurance
Quality - Manager, Quality
Amphenol and its Affiliated Companies —Fremont, CA
- $110,000 - $150,000 a year
- Full-time
- 7 years
- Engineering
- Master's degree
- Health savings account
- Paid holidays
Quick Apply
14d

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Manager, Quality Assurance

THINK Surgical, Inc.
Fremont, CA

Quick Apply

Job Details

Full-time
$165,000 - $180,000 a year

Qualifications

Regulatory inspections
Investigations regulatory compliance
Defect resolution root cause analysis
Team supervision
Preventive action implementation
Production deviation management
Compliance audits & assessments
Quality control preventive actions
Corrective and preventive actions (CAPA)
Internal investigations
ISO certification audits
Quality control audit
Biomedical regulatory compliance
Process improvement planning
Cross-functional collaboration
General management
Cross-functional communication
FDA regulations
Audit support
Failure analysis

Full Job Description

JOB SUMMARY

The Manager, Quality Assurance is responsible for leading and ensuring the effective execution, compliance, and continuous improvement of core Quality Management System (QMS) processes, including Corrective and Preventive Action (CAPA), Complaint Handling, Nonconformance Management, Internal and External Audits, and overall regulatory compliance. This role provides operational and strategic leadership to ensure that quality system processes are compliant with applicable regulatory requirements, including FDA Quality Management System Regulation (21 CFR Part 820/QMSR), ISO 13485, and other global standards. The Manager, Quality Assurance is accountable for driving timely and effective investigations, risk-based decision making, and inspection readiness across the organization. The position leads a team of quality professionals and works cross-functionally throughout the organization to ensure product quality, patient safety, and regulatory compliance. This position is based in THINK’s corporate office.

DUTIES & RESPONSIBILITIES

Lead and manage the CAPA, Complaint Handling, Nonconformance, and Audit programs to ensure compliance, effectiveness, and continuous improvement.
Ensure quality system processes are aligned with FDA (21 CFR Part 820/QMSR), ISO 13485, and other applicable regulatory requirements.
Establish and maintain a risk-based framework for escalation, prioritization, and resolution of quality issues across CAPA, complaints, and nonconformances.
Drive timely and thorough investigations, including root cause analysis, correction, corrective action, and verification of effectiveness (VOE).
Oversee complaint handling processes, ensuring accurate evaluation, investigation, and regulatory reporting (e.g., MDR) as required.
Ensure nonconformances (material and process) are appropriately documented, evaluated, and dispositioned, with clear escalation pathways to CAPA when required.
Serve as the subject matter expert (SME) for CAPA, complaints, nonconformance, and audit processes.
Ensure processes incorporate risk-based decision making consistent with QMSR expectations.
Ensure alignment and integration across quality system processes to avoid silos and drive systemic effectiveness.
Lead internal audit programs, including audit planning, execution, reporting, and follow-up of audit findings.
Support external audits and inspections (FDA, notified bodies, customers), including preparation, hosting, and response activities.
Ensure inspection readiness through robust documentation, metrics, and process discipline.
Develop and monitor key quality metrics (e.g., CAPA timeliness, complaint cycle time, audit findings, backlog trends) and drive data-driven decision making.
Identify systemic quality issues and drive cross-functional continuous improvement initiatives.
Ensure effective implementation and maintenance of quality system procedures, work instructions, and records.
Collaborate with cross-functional teams to ensure compliance with product and process requirements.
Provide leadership in regulatory compliance strategy as it relates to quality system processes.
Support management review by providing meaningful data, trends, and recommendations.

SUPERVISORY RESPONSIBILITIES

Direct management of Quality Assurance personnel, including Compliance, Complaints, Supplier Quality, Quality Engineering, and Inspection functions.
Provide coaching, mentoring, and performance management to ensure a high-performing team.
Establish clear roles, responsibilities, and accountability within the team.
Handle discipline and termination of employees in accordance with company policy.
Drive a culture of quality, compliance, and continuous improvement across the organization.
Ensure adequate resourcing and prioritization aligned with business and regulatory needs.

QUALIFICATIONS

Required:

Bachelor’s degree in engineering, science, or a related discipline, or an equivalent combination of education and experience.
Minimum of 10 years of experience in Quality Assurance within the medical device or similarly regulated industry.
Minimum 3 years of leadership or people management experience.
Strong working knowledge of FDA 21 CFR Part 820/QMSR and ISO 13485 requirements, along with direct experience managing CAPA, complaint handling, nonconformance, and audit processes.
Experience supporting FDA inspections and/or notified body audits is required.
Proven ability to lead complex investigations, perform robust root cause analysis, and drive effective corrective actions.
Experience developing and monitoring quality metrics, as well as driving continuous improvement initiatives.
Strong written and verbal communication skills are essential, along with excellent organizational, analytical, and problem-solving abilities.
Ability to influence cross-functional stakeholders and drive accountability across the organization is critical for success in this role.
Knowledge of Good Manufacturing Practices (GMP) and applicable Quality System Standards.

Preferred:

Professional certifications such as Certified Quality Auditor (CQA), Certified Quality Engineer (CQE), or ISO 13485 Lead Auditor.
Experience working with medical device software, robotics, or other complex systems.
Experience implementing or transforming Quality Management System processes.
Familiarity with Salesforce.com based electronic QMS platforms such as Propel.

COMPETENCIES

Drive Results

Decision quality
Leadership and team development
Risk-based thinking
Process optimization
Collaboration and cross-functional Influence

PHYSICAL DEMANDS & WORK ENVIRONMENT

Must be able to remain in a stationary position and operate office equipment for a prolonged period of time.
Physical activities include, but not limited to constant manual dexterity, moving about the work site, and/or handling objects weighing up to 20 lbs.
Other infrequent physical activities include, but not limited to, positioning self to complete assigned tasks, and ascending/descending floors and/or ladders.
Occasionally work around moving mechanical parts.
Must be able to work in a schedule that commensurate with business operation, including work during weekends, holidays and/or times outside of normal business hours.
Must be able to travel as business necessitates (up to 10%).

Disclaimer:

The above is intended to describe the general content of and requirements for the performance of this job. It is not to be construed as an exhaustive statement of duties, responsibilities, or physical requirements. Nothing in this job description restricts management’s right to assign or reassign duties and responsibilities to this job at any time. Reasonable accommodations may be possible to enable individuals with disabilities to perform the essential functions.

THINK Surgical, Inc. (“THINK”) is committed to hiring the best qualified candidates for approved positions while engaging in recruitment and selection practices that are in compliance with all applicable employment laws. It is the policy of THINK to provide equal employment opportunity for employment to all applicants and employees, regardless of any protected status. Any qualified applicant or employee with a disability who requires an accommodation in connection with their employment at THINK should contact Human Resources and request an accommodation. THINK also participates in E-Verify, a web-based system that allows THINK to confirm an employee’s eligibility to work in the United States. Actual compensation offered will depend on several factors including but not limited to geographic location, work experience, education, skill level, and/or other business and organizational needs

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Refine Your Search

quality manager jobs in san mateo, ca

Manager, Quality Assurance

Quality Manager

Quality Assurance Manager, Home

Senior Quality Operations Manager

Manager, Clinical Quality

Director of Quality Assurance

Quality Control Manager

Senior Manager, Quality Systems - Lingo (on-site)

Manager, Quality Assurance

Supervisor, Quality Inspector (Day Shift)

Quality Engineering Manager

Senior Manager, Quality Assurance Program

Quality Engineering, Manager

Senior Manager Quality Assurance

Manager, Quality & Safety

QA Manager, Training Services

Document Control Manager

Quality Assurance Supervisor

Senior Manager, Quality Assurance (GMP Operations)

Quality - Manager, Quality

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