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Project Manager Quality Systems Jobs in San Ramon, CA

Effectively manage multiple tasks and drive execution of change orders * Initiate and/or support ... We are looking for quality systems engineers with at least 2 years of industry experience.

Effectively manage multiple tasks and drive execution of change orders * Initiate and/or support ... We are looking for quality systems engineers with at least 2 years of industry experience.

Quality System Manager

San Jose, CA · On-site

$105K - $135K/yr

The Quality Management Systems Manager will provide leadership in the implementation, maintenance ... Execute projects and complete other duties as assigned. Please note that this position requires ...

Quality System Manager

San Jose, CA · On-site

$105K - $135K/yr

The Quality Management Systems Manager will provide leadership in the implementation, maintenance ... Execute projects and complete other duties as assigned. Please note that this position requires ...

Ensure effective and efficient roll-out of quality management system changes * Maintain accurate documentation of QMS * Lead effective ongoing QMS training * For some QMS elements, provide direct ...

Sr. Quality Systems Engineer

San Jose, CA · On-site

$128K - $192K/yr

Ensure effective and efficient roll-out of quality management system changes * Maintain accurate documentation of QMS * Lead effective ongoing QMS training * For some QMS elements, provide direct ...

Site quality systems development and continual improvement, working within the site teams to maintain ISO9001, AS9100 certifications and other industry standards * Site Quality Management Plan to ...

Showing results 21-40

Project Manager Quality Systems information

See San Ramon, CA salary details

$84.4K

$130.7K

How much do project manager quality systems jobs pay per year?

As of Sep 10, 2026, the average yearly pay for project manager quality systems in San Ramon, CA is $130,062.00, according to ZipRecruiter salary data. Most workers in this role earn between $130,200.00 and $130,200.00 per year, depending on experience, location, and employer.

What is a project manager quality systems?

A Project Manager Quality Systems is a professional responsible for overseeing the planning, implementation, and maintenance of quality management systems within an organization. They ensure that processes and deliverables meet regulatory standards and internal quality benchmarks throughout a project's lifecycle. This role often involves coordinating cross-functional teams, developing quality assurance protocols, conducting audits, and driving continuous improvement initiatives. Project Manager Quality Systems play a critical role in industries such as healthcare, manufacturing, and pharmaceuticals, where adherence to quality standards is essential.

How does a project manager quality systems typically collaborate with cross-functional teams to achieve quality objectives?

A Project Manager Quality Systems works closely with cross-functional teams, including engineering, manufacturing, regulatory, and quality assurance, to ensure that quality standards are integrated into every stage of a project. This often involves leading meetings, facilitating communication between departments, and aligning project goals with compliance requirements. Effective collaboration is key to identifying potential quality risks early and implementing corrective actions promptly. By fostering a culture of quality and continuous improvement, the Project Manager helps teams stay focused on delivering consistent, high-quality results.

What are the key skills and qualifications needed to thrive as a project manager quality systems, and why are they important?

To thrive as a Project Manager Quality Systems, you need strong project management abilities, a solid understanding of quality assurance principles, and typically a relevant degree such as engineering or life sciences. Familiarity with quality management systems (QMS), regulatory compliance standards (like ISO 9001), and project management tools (such as MS Project or Jira) is essential. Outstanding communication, leadership, and problem-solving skills help you drive cross-functional collaboration and continuous improvement. These competencies are vital to ensure projects are delivered efficiently while meeting stringent quality and regulatory requirements.

What is the difference between Project Manager Quality Systems vs Quality Assurance Specialist?

AspectProject Manager Quality SystemsQuality Assurance Specialist
CertificationsISO 9001 Lead Auditor, PMPISO 9001 Lead Auditor, CQE
Work EnvironmentCross-departmental, project-focusedQuality department, compliance-focused
Employer & Industry UsageManufacturing, pharma, techManufacturing, healthcare, biotech

The Project Manager Quality Systems oversees quality projects, ensuring compliance and process improvements across departments. The Quality Assurance Specialist focuses on maintaining quality standards, conducting audits, and ensuring product compliance. While both roles require similar certifications and work within quality frameworks, the project manager emphasizes managing initiatives, whereas the QA specialist concentrates on compliance and testing.

What cities near San Ramon, CA are hiring for Project Manager Quality Systems jobs?

Cities near San Ramon, CA with the most Project Manager Quality Systems job openings:

Infographic showing various Project Manager Quality Systems job openings in San Ramon, CA as of August 2026, with employment types broken down into 1% As Needed, 76% Full Time, 18% Part Time, 4% Contract, and 1% Nights. Highlights an 88% Physical, 2% Hybrid, and 10% Remote job distribution, with an average salary of $130,062 per year, or $62.5 per hour.

Quality Systems Specialist

Redwood City, CA • On-site

Element Science
Medical Equipment and Supplies Manufacturing • 1 - 10 employees

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 3 days ago


Job description

Element Science, Inc. is a medical device and digital health company redefining how patients with heart disease are monitored and treated as they transition from the hospital to the home. Our mission is to improve outcomes for patients at risk of life-threatening cardiac events through innovative solutions at the intersection of clinical-grade wearables, advanced algorithms, and therapy delivery. 

We are entering an exciting phase of growth as we move from development into early commercialization. Our approach combines hardware, software, and services to deliver a more personalized and seamless patient experience—designed with both patients and clinicians in mind. Our product, a wearable patch defibrillator, is designed for patients with a temporary elevated risk of sudden cardiac arrest, addressing a significant and underserved population of over 500,000 patients in the U.S. By focusing on comfort, usability, and clinical effectiveness, we aim to transform the standard of care during this critical period. Headquartered in the San Francisco Bay Area, Element Science is backed by leading healthcare and technology investors, including Third Rock Ventures, GV (Google Ventures), Deerfield Healthcare, Cormorant Asset Management, and Invus Opportunities.

SUMMARY OF ROLE:

We are looking for a Quality Systems Specialist II with passion for creating devices that save lives. The  Quality Systems Specialist II works closely with cross-functional teams to assist in key quality initiatives, including Complaint Management, Change Control, NCR (Non-Conformance Report) Management, CAPA (Corrective and Preventive Actions), and more. This position will play a vital role in guiding teams, ensuring compliance with industry regulations, and supporting various quality improvement efforts. If you are passionate about ensuring product quality and regulatory compliance, we would love to talk to you.

RESPONSIBILITIES:

  • Support the CAPA processes by facilitating investigations, tracking progress, and ensuring that corrective and preventive actions are implemented effectively.
  • Perform investigations for Quality-owned CAPAs, analyzing root causes, identifying corrective and preventive actions.
  • Work closely with teams including Manufacturing Engineering, Quality Engineering, Regulatory Affairs, R&D, and Production to support quality initiatives and ensure compliance with QMS requirements.
  • Review ECOs as a Quality SME and provide feedback and guidance on the impact of changes and help ensure changes are implemented in compliance with internal procedures and regulatory standards.
  • Assist in the review, routing, and approval of QMS documentation, ensuring all records are accurate, complete, and meet regulatory and quality standards. Follow up with stakeholders to ensure timely approval and completion of documentation tasks.
  • Provide guidance and support to team members and peers in understanding and following QMS processes. Assist with training activities and contribute to a culture of continuous learning and improvement.
  • Collect, analyze, and report on key quality metrics related to complaints, NCRs, CAPAs, and other QMS processes. Help track trends and provide insights to identify areas for process improvements.
  • Support internal and external audits, ensuring compliance with ISO 13485, QMSR, and other applicable regulations. Support the resolution of audit findings and help implement corrective actions.
  • Support DME/CHAP quality documentation requirements as applicable to the company's distribution model.
  • Assist in Post-Market Surveillance activities, tracking and analyzing product performance data to identify potential quality issues or trends that require attention.
  • Lead or participate in various quality improvement initiatives, helping to identify opportunities for process optimization and supporting the implementation of changes to enhance quality performance.
  • Other tasks as assigned by the management.

QUALIFICATIONS:

  • Bachelor's degree in a scientific or engineering discipline or related discipline. 
  • 3+ years of relevant experience in a Medical Device environment with a focus on Quality Systems
  • Demonstrates strong knowledge of current ISO 13485 standard and QMSR.
  • Strong ability to collaborate with cross-functional teams, providing guidance and input on various quality initiatives.
  • Excellent communication skills (written and verbal), with the ability to clearly explain and assist others with QMS processes and requirements.
  • Strong organizational skills, with the ability to manage multiple tasks, prioritize effectively, and meet deadlines in a fast-paced environment.
  • Experience with Propel or similar eQMS platform strongly preferred.
  • Strong problem-solving and analytical skills, with the ability to interpret data and make informed decisions.
  • Ability to work independently and take ownership of tasks while collaborating with others to meet common goals.
  • Prior experience preparing for or leading an internal, external, or regulatory audit.

BENEFITS:

Element Science offers a very competitive salary and benefits package including, but not limited to:

  • Stock Options
  • 90% employer-paid medical, dental, and vision insurance
  • Company-paid Basic Life Insurance
  • 401(k) retirement plan (Traditional and Roth)
  • Competitive Paid Time Off
  • Paid Holidays
  • FSA (Flexible Spending Accounts)
  • HSA (Health Savings Account)
  • Employee Assistance Program through PEO

The salary for this exempt-level position will be based on experience and qualifications within an established pay range.

  • Pay range: $87,000 - $100,000 + Annual Bonus

Element Science is an Equal Opportunity Employer.  All candidates will be evaluated on the basis of their qualifications for the job in question. We do not base our employment decision on an employee's or applicant's race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, genetic information (including family medical history), political affiliation, military service, or other non-merit-based factors prohibited by local, state, or federal law. 

In compliance with federal law, all persons hired will be required to verify identity and eligibility to work in the United States and to complete the required employment eligibility verification form upon hire.  We are not able to sponsor individuals for employment visas for this job.  

At this time, we are unable to offer relocation assistance at Element Science.