Top 44 Director of quality assurance Jobs in Milpitas, Ca

Associate Director, Quality
Baxter —Hayward, CA
- $160,000 - $220,000 a year
- 7 years
- Engineering
- Analysis skills
- Paid parental leave
- Employee stock purchase plan
Sr. Director, Quality Assurance for Quality Control
Vaxcyte —San Carlos, CA
- $229,000 - $268,000 a year
- 11+ years
- Bachelor's degree
- Senior level
Quality Assurance Director
Viant Medical —Fremont, CA
- $200,000 - $240,000 a year
- Full-time
- Word processing
- Computer literacy
- Writing skills
- Paid holidays
- Disability insurance
Quick Apply
3d
Director Quality and Mission Assurance
Honeywell Aerospace —San Jose, CA
- Full-time
- Management
- Senior level
Associate Director, Quality Assurance - CMC Operations
Protagonist Therapeutics —Newark, CA
- $175,000 - $225,000 a year
- Full-time
- Office
- Bachelor's degree
- Travel
- Wellness program
- Commuter assistance
Quick Apply
12d
Associate Director, QC Global Analytics
Vaxcyte —San Carlos, CA
- $176,000 - $206,000 a year
- Remote
- Analysis skills
- Bachelor's degree
- Mentoring
Head of Quality Assurance
Aspect Biosystems —Fremont, CA
- $191,000 - $202,000 a year
- Master's degree
- Doctor of Philosophy
- Mentoring
Quick Apply
Associate Director, Quality Assurance (Global Supplier Quality)
Gilead Sciences —Foster City, CA
- $165,495 - $235,620 a year
- Full-time
- Analysis skills
- Bachelor's degree
- Senior level
- Health insurance
- Dental insurance
Director of Quality Assurance
Vital Connect Inc —San Jose, CA
- $200,000 - $230,000 a year
- Management
- 8 years
- Bachelor's degree
- Dental insurance
Quick Apply
Director, Quality
Toray Advanced Composites USA,Inc —Morgan Hill, CA
- $175,000 - $205,000 a year
- Full-time
- Word processing
- Engineering
- 11+ years
- Health savings account
- AD&D insurance
Quick Apply
Senior Director / Director - CMC/GMP Quality Assurance
Semnur, Inc. —Palo Alto, CA
- $235,000 - $285,000 a year
- Full-time
- Hybrid work
- Adults
- Office
- Contracts
Quick Apply
Director, Quality Assurance Operations
Adicet Bio —Redwood City, CA
- $199,000 - $274,000 a year
- Full-time
- 5 years
- Office
- Bachelor's degree
- Free parking
- Paid parental leave
Director of Module Manufacturing
Renesas Electronics —San Jose, CA
- $196,000 - $240,000 a year
- Full-time
- Management
- Master's degree
- Manufacturing
Quick Apply
Senior Director, Reliability Engineering
NVIDIA —Santa Clara, CA
- $332,000 - $500,250 a year
- Full-time
- Engineering
- Analysis skills
- Math
Sr. Manager / Associate Director, Quality Audits
Personalis, Inc —Fremont, CA
- $165,000 - $210,000 a year
- Full-time
- Hybrid work
- Microsoft Excel
- 8 years
- Analysis skills
- Commuter assistance
- Employee stock purchase plan
Associate Director of QC / HPLC
Asahi Kasei —Fremont, CA
- $155,000 - $200,000 a year
- Full-time
- 6 years
- Bachelor of Science
- Bachelor's degree
- Health insurance
- Dental insurance
Associate Director, Quality Assurance (GMP Operations)
Gilead Sciences —Foster City, CA
- $182,070 - $235,620 a year
- Full-time
- 5 years
- Bachelor's degree
- Doctor of Philosophy
- Health insurance
- Dental insurance
Director, Quality Assurance *PC 586
Miltenyi Biotec, Inc. —San Jose, CA
- $212,237 - $249,690 a year
- Bachelor of Science
- Doctor of Philosophy
- Senior level
- Health insurance
- Dental insurance
Quick Apply
Director - Product Quality Complaints
Gilead Sciences —Foster City, CA
- $191,250 - $272,250 a year
- Full-time
- Bachelor's degree
- Doctor of Philosophy
- Senior level
- Health insurance
- Dental insurance
Director, Quality Assurance Compliance
Gilead Sciences —Foster City, CA
- $210,375 - $272,250 a year
- Full-time
- 5 years
- Presentation skills
- Organizational skills
- Health insurance
- Dental insurance
4d

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Associate Director, Quality

Baxter -
Hayward, CA

Apply Now

Job Details

$160,000 - $220,000 a year

Benefits

Paid parental leave
Employee stock purchase plan
Paid holidays
Disability insurance
Health insurance
Dental insurance
401(k)
Flexible spending account
Tuition reimbursement
Paid time off
Parental leave
Employee assistance program
Employee discount

Qualifications

Regulatory inspections
Succession planning
Performance improvement leadership
7 years
Program management
Microbiology
ISO standards
Preventive action implementation
Coaching
Engineering
Providing information to customers
Direct client contact
Corrective and preventive actions (CAPA)
GMP
Cleanroom protocols
Performance management
Microbiology
Global team management
Manufacturing facility experience
Team development
Analysis skills
Policy & process development
Bachelor's degree in engineering
Professional development support
Quality risk management
Budget planning
Cleanroom gowning procedures
Decision making
Team training
Technology transfer (scale-up process)

Full Job Description

Req # 206344 Location Hayward, California, United States Job Category Quality Date posted 08/06/2026

Overview

This is where you make a difference in our patients’ safety. As a member of the Baxter Quality team, you will play an essential part in our mission of saving and sustaining lives. Quality is important throughout the entire product lifecycle and works collaboratively with all areas of the organization. Because Quality touches everything Baxter does, a role in Quality provides many opportunities for growth, learning and a successful career that has a daily impact on people’s lives.

Support for Parents
Continuing Education/ Professional Development
Employee Heath & Well-Being Benefits
Paid Time Off
2 Days a Year to Volunteer

Success Profile

What makes a successful Quality team member at Baxter? Take a look at some of the top traits we’re looking for and see if you’re a fit.

Detail Oriented
Continuous Learner
Courageous
Collaborative
Critical Thinker
Influential

This is where your work makes a difference.

At Baxter, we believe every person—regardless of who they are or where they are from—deserves a chance to live a healthy life. It was our founding belief in 1931 and continues to be our guiding principle. We are redefining healthcare delivery to make a greater impact today, tomorrow, and beyond.

Our Baxter colleagues are united by our Mission to Save and Sustain Lives. Together, our community is driven by a culture of courage, trust, and collaboration. Every individual is empowered to take ownership and make a meaningful impact. We strive for efficient and effective operations, and we hold each other accountable for delivering exceptional results.

Here, you will find more than just a job—you will find purpose and pride.

Your Role

This position is responsible for being Most Senior plant level Quality Management Representative, developing and deploying the quality system for the plant, assuring systems and procedures for regulatory compliance are established and deployed

What You'll Be Doing

Serve as the Management Representative for Quality and lead the Quality organization within a mid-to-large manufacturing facility.
Build and develop a high-performing Quality organization with a clear vision and mission that supports business growth and global expansion.
Oversee batch review and product release activities.
Fulfill the responsibilities of the Person Responsible for Regulatory Compliance (PRRC), including ensuring device conformity is appropriately verified in accordance with the Quality Management System before release.
Ensure Post-Market Surveillance (PMS) obligations are fulfilled.
Ensure vigilance reporting requirements are met in accordance with Articles 87-91 of the Medical Device Regulation (MDR).
Direct large-scale programs and departmental initiatives in support of division-wide and company-wide objectives.
Maintain accountability for product quality, regulatory compliance, and adherence to Baxter quality policies.
Develop, implement, and maintain quality systems, including Management Review, CAPA, Design Controls, and Process Controls, to ensure products meet defined requirements.
Ensure compliance with applicable regulatory requirements and manage regulatory inspections and audits.
Conduct periodic reviews of the Quality Management System with executive leadership to ensure effectiveness and continued suitability.
Drive continuous improvement initiatives across processes and systems while supporting deployment of divisional and corporate quality programs.
Assess and advise senior leadership on quality-related aspects of acquisition targets.
Collaborate effectively with stakeholders across functions, business units, and global locations.
Serve as the primary quality representative in interactions with customers and regulatory agencies regarding products, systems, and processes.
Ensure adherence to established specifications, procedures, and standards supporting product quality and regulatory compliance.
Develop and manage the Quality organization budget and ensure effective utilization of departmental resources.
Lead coaching, training, performance management, employee development, and succession planning initiatives for the Quality team.

What You'll Bring

In-depth knowledge of the regulatory environment governing the manufacture of medical devices and therapeutics.
Proven leadership experience managing large teams in a complex, regulated environment.
Demonstrated ability to lead within a matrix organization and collaborate effectively across global, cross-functional teams.
Strong analytical, problem-solving, and decision-making skills.
Excellent verbal and written communication skills.
Proven success working with multifunctional and global teams.
Strong interpersonal, influencing, and negotiation skills.
Extensive knowledge of applicable quality systems, regulatory standards, and industry regulations.
Experience in risk management, validation, analytics, and microbiology within a GMP-regulated environment.
Quality expertise supporting technology transfer initiatives.
Ability and willingness to work within ISO 7 and ISO 8 cleanroom manufacturing environments, including required gowning procedures.

Education & Experience

Bachelor's degree in Science, Engineering, or a related technical discipline required; advanced degree preferred.
Minimum of 10 years of experience in Quality, Manufacturing, or a related field within the medical products industry.
Minimum of 7 years of management experience.

We understand compensation is an important factor as you consider the next step in your career. At Baxter, we are committed to equitable pay for all employees, and we strive to be more transparent with our pay practices. The estimated base salary for this position is $160,000 - $220,000 annually. The estimated salary is meant to reflect an anticipated salary range for the position. We may pay more or less than the anticipated range based upon market data and other factors, all of which are subject to change. Individual pay is based on location, skills and expertise, experience, and other relevant factors. This position may also be eligible for discretionary bonuses. For questions about this, our pay philosophy, and available benefits, please speak to the recruiter if you decide to apply and are selected for an interview.

Applicants must be authorized to work for any employer in the U.S. We are unable to sponsor or take over sponsorship of an employment visa at this time.

US Benefits at Baxter (except for Puerto Rico)

This is where your well-being matters. Baxter offers comprehensive compensation and benefits packages for eligible roles. Our health and well-being benefits include medical and dental coverage that start on day one, as well as insurance coverage for basic life, accident, short-term and long-term disability, and business travel accident insurance. Financial and retirement benefits include the Employee Stock Purchase Plan (ESPP), with the ability to purchase company stock at a discount, and the 401(k) Retirement Savings Plan (RSP), with options for employee contributions and company matching. We also offer Flexible Spending Accounts, educational assistance programs, and time-off benefits such as paid holidays, paid time off ranging from 20 to 35 days based on length of service, family and medical leaves of absence, and paid parental leave. Additional benefits include commuting benefits, the Employee Discount Program, the Employee Assistance Program (EAP), and childcare benefits. Join us and enjoy the competitive compensation and benefits we offer to our employees. For additional information regarding Baxter US Benefits, please speak with your recruiter or visit our Benefits site: Benefits | Baxter

Equal Employment Opportunity

Baxter is an equal opportunity employer. Baxter evaluates qualified applicants without regard to race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, protected veteran status, disability/handicap status or any other legally protected characteristic.

Know Your Rights: Workplace Discrimination is Illegal

Reasonable Accommodations

Baxter is committed to working with and providing reasonable accommodations to individuals with disabilities globally. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process, please click on the link here and let us know the nature of your request along with your contact information.

Recruitment Fraud Notice

Baxter has discovered incidents of employment scams, where fraudulent parties pose as Baxter employees, recruiters, or other agents, and engage with online job seekers in an attempt to steal personal and/or financial information. To learn how you can protect yourself, review our Recruitment Fraud Notice.

Apply Now

Refine Your Search

director of quality assurance jobs in milpitas, ca

Associate Director, Quality

Sr. Director, Quality Assurance for Quality Control

Quality Assurance Director

Director Quality and Mission Assurance

Associate Director, Quality Assurance - CMC Operations

Associate Director, QC Global Analytics

Head of Quality Assurance

Associate Director, Quality Assurance (Global Supplier Quality)

Director of Quality Assurance

Director, Quality

Senior Director / Director - CMC/GMP Quality Assurance

Director, Quality Assurance Operations

Director of Module Manufacturing

Senior Director, Reliability Engineering

Sr. Manager / Associate Director, Quality Audits

Associate Director of QC / HPLC

Associate Director, Quality Assurance (GMP Operations)

Director, Quality Assurance *PC 586

Director - Product Quality Complaints

Director, Quality Assurance Compliance

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