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Qms Manager Jobs in California (NOW HIRING)

Avid Bioservices

Technical Specialist, QMS

Tustin, CA · On-site

$54K - $68K/yr

The Technical Specialist, QMS is responsible for writing records for Avid's Quality Management System (QMS) including, but not limited to, records for the following: Deviations, out-of-tolerance ...

Avid Bioservices

Technical Specialist, QMS

Tustin, CA · On-site

$54K - $68K/yr

The Technical Specialist, QMS is responsible for writing records for Avid's Quality Management System (QMS) including, but not limited to, records for the following: Deviations, out-of-tolerance ...

Alphatec Spine

Systems Analyst- PLM/QMS

Carlsbad, CA · On-site

... System (QMS) requirements. The PLM Analyst partners closely with R&D, Quality, Regulatory ... Manage and support ECO, MCO, CR, Deviations, and other change workflows. * Ensure accurate routing ...

Orca Bio

Senior Specialist, Global QMS

Sacramento, CA · On-site

$90 - $120/hr

The Senior Specialist, Global QMS will help implement Orca Bio's global quality management system across all sites. This role will support and lead the internal audit program, supplier management ...

Orca Bio

Senior Specialist, Global QMS

Sacramento, CA · On-site +1

$90K - $120K/yr

The Senior Specialist, Global QMS will help implement Orca Bio's global quality management system across all sites. This role will support and lead the internal audit program, supplier management ...

Orca Bio

Senior Specialist, Global QMS

Sacramento, CA · On-site +1

$90K - $120K/yr

The Senior Specialist, Global QMS will help implement Orca Bio's global quality management system across all sites. This role will support and lead the internal audit program, supplier management ...

Socket.dev

Senior Specialist, Global QMS

Sacramento, CA · On-site

$150 - $210/hr

The Senior Specialist, Global QMS will help implement Orca Bio's global quality management system across all sites. This role will support and lead the internal audit program, supplier management ...

New

Alphatec Spine

Systems Analyst- PLM/QMS

Carlsbad, CA

$110K - $125K/yr

... System (QMS) requirements. The PLM Analyst partners closely with R&D, Quality, Regulatory ... Manage and support ECO, MCO, CR, Deviations, and other change workflows. * Ensure accurate routing ...

Alphatec Spine

Systems Analyst- PLM/QMS

Carlsbad, CA · On-site

$110K - $125K/yr

... System (QMS) requirements. The PLM Analyst partners closely with R&D, Quality, Regulatory ... Manage and support ECO, MCO, CR, Deviations, and other change workflows. * Ensure accurate routing ...

Avid Bioservices

Technical Specialist, QMS

Tustin, CA · On-site

$54.40 - $68/hr

Your Role: The Technical Specialist, MQS is responsible for writing records for Avid's Quality Management System (QMS) including, but not limited to, records for the following: Deviations ...

MWI Buying Group

Quality Assurance Manager

Hawthorne, CA · On-site

$74 - $147/hr

QMS Management: Developing and maintaining a robust QMS that defines the organization's quality objectives, policies, procedures, and performance metrics. This includes acting as a first contact for ...

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Showing results 21-40

All JobsQms JobsQms Manager JobsQms Manager Jobs in California

Qms Manager information

See California salary details

$23.7K

$85K

$155.9K

How much do qms manager jobs pay per year?

As of Sep 3, 2026, the average yearly pay for qms manager in California is $85,031.00, according to ZipRecruiter salary data. Most workers in this role earn between $43,400.00 and $134,200.00 per year, depending on experience, location, and employer.

What is a QMS manager?

QMS Managers, or Quality Management System Managers, are professionals responsible for developing, implementing, and overseeing an organization's quality management system. They ensure that processes and products meet established quality standards and comply with relevant regulations. Their duties often include conducting audits, managing documentation, training staff on quality procedures, and driving continuous improvement initiatives. QMS Managers play a crucial role in maintaining customer satisfaction and supporting organizational efficiency.

How does a QMS manager typically collaborate with other departments to ensure compliance and continuous improvement?

A QMS Manager regularly works cross-functionally with departments such as production, engineering, and procurement to implement and maintain quality standards. This involves coordinating audits, facilitating training sessions, and gathering feedback to identify areas for process improvement. Effective communication and negotiation skills are essential, as the QMS Manager must align diverse teams toward compliance goals and foster a culture of continuous improvement. Regular meetings and collaborative problem-solving are part of ensuring that quality objectives are met across the organization.

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

To thrive as a QMS Manager, you need expertise in quality management systems, regulatory compliance, and process improvement, typically supported by a relevant degree and experience in quality assurance. Familiarity with ISO standards (such as ISO 9001), audit management tools, and quality software platforms is essential. Strong leadership, problem-solving skills, and effective communication help drive a culture of continuous improvement and team alignment. These competencies ensure that organizational processes meet regulatory requirements and consistently deliver high-quality outcomes.

What is the difference between Qms Manager vs Quality Assurance Supervisor?

AspectQms ManagerQuality Assurance Supervisor
CertificationsISO 9001 Lead Auditor, CQEISO 9001 Lead Auditor, CQE
Work EnvironmentOversees quality management systems across departmentsSupervises quality assurance team and daily testing activities
Industry UsageUsed in manufacturing, aerospace, automotiveCommon in manufacturing, pharmaceuticals, food industry
Primary FocusDeveloping, maintaining, and improving QMSMonitoring product quality and compliance

The Qms Manager and Quality Assurance Supervisor roles share similar certifications and industry usage, but the Qms Manager focuses on managing the entire quality management system, while the Supervisor concentrates on daily quality assurance activities. Both positions are vital for ensuring product quality and compliance within manufacturing and related industries.

What are the most commonly searched types of Qms jobs in California?

The most popular types of Qms jobs in California are:

What are popular job titles related to Qms Manager jobs in California?

For Qms Manager jobs in California, the most frequently searched job titles are:

What job categories do people searching Qms Manager jobs in California look for?

The top searched job categories for Qms Manager jobs in California are:

What cities in California are hiring for Qms Manager jobs?

Cities in California with the most Qms Manager job openings:

Qms Manager jobs near you
Infographic showing various Qms Manager job openings in California as of August 2026, with employment types broken down into 85% Full Time, 14% Part Time, and 1% Contract. Highlights an 87% Physical, 2% Hybrid, and 11% Remote job distribution, with an average salary of $85,031 per year, or $40.9 per hour.

Technical Specialist, QMS

Avid Bioservices

Tustin, CA • On-site

$54K - $68K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Re-posted 18 days ago

Job description

Description
Looking to join a passionate team dedicated to developing and manufacturing life-saving biopharmaceuticals? Avid Bioservices is a leading clinical and commercial biologics CDMO focused on creating innovative solutions to meet the needs of our clients and improve patient outcomes.
Your Role:
The Technical Specialist, QMS is responsible for writing records for Avid's Quality Management System (QMS) including, but not limited to, records for the following: Deviations, out-of-tolerance calibration events, out-of-specification (OOS) results, out-of-limit (OOL) results, and out-of-trend (OOT) results. This role performs investigations required to write these records and for routing/tracking records from assignment to approval. Identifies and implements corrective and preventive actions (CAPAs), as applicable. Where issues or improvements are identified, this role works with subject matter experts to propose viable solutions including a final product impact assessment. Identifies elements that can be made more efficient, are potential sources of discrepancies, require 'fine-tuning', or need a complete revision.
Key Responsibilities:
  • Adhere to Good Manufacturing Practice (GMP) regulations (21 CFR, Part 211) and Good Documentation Practices (GDP), as applicable.
  • Investigate root causes of a variety of events, with reference to related source documents including, but not limited to, procedures, protocols, reports, batch records, laboratory data, and calibration data; apply relevant scientific and technical principles during investigation.
  • Write QMS records with excellent attention to detail; ensure records accurately present the facts determined during investigation.
  • Adhere to procedures that define requirements for each record type.
  • Adhere to rules for correct grammar, usage, and mechanics; write clear and understandable text, using a narrative approach where applicable; revise based on redlines and comments from subject matter experts, management, and QA.
  • Proactively interface with witnesses and subject matter experts to gather information; interface with Quality Assurance (QA) on questions related, but not limited, to: GMP compliance, Avid procedures and processes, investigation requirements, and record quality and style.
  • Manage each record from the time it is assigned through closure; work with all stakeholders to ensure record is closed according to defined timelines.
  • Manage multiple records and projects simultaneously.
  • Ability to perform statistical analysis of data to form conclusions and recommendations.
  • Other tasks as assigned.

Minimum Qualifications:
  • B.S. degree in science or engineering (biological, chemical, or biomedical.
  • 2+ years of technical writing experience, or an equivalent combination of relevant education and experience.
  • Excellent technical writing skills.
  • Experience with writing QMS documents preferred.
  • Expert experience in the use of MS Word.

Position Type/Expected Hours of Work:
This role is a full-time, exempt position. Days of work are Monday through Friday unless otherwise stated by the Supervisor or needed due to projects. Must be available to work holidays, weekends, or extended hours when needed.
Compensation:
We offer competitive compensation packages for this role, including a base salary, performance-based bonuses, and comprehensive benefits such as health, dental, and vision insurance, 401(k) matching, and paid time off.
The compensation range for this role is $54,400 - $68,000 annually depending on experience and qualifications. Additionally, we offer opportunities for career growth and development as well as a supportive and inclusive work environment.
Who you are:
  • You have a "bring it on!" team player approach and an unshakable positive attitude, always ready to tackle anything that comes your way.
  • Your written and verbal skills are out of this world, and you communicate with clarity and confidence.
  • You have exceptional multitasking skills and an unparalleled attention to detail that ensure the smooth running of everything.
  • You are a master at building relationships, capable of establishing connections with anyone, be it team members, clients, vendors, or suppliers.

Physical Demands & Work Environment:
In this dynamic role, expect a blend of regular activities like sitting, standing, and walking, with occasional physically engaging tasks such as lifting objects up to 20 pounds. The work environment might expose you to electrical shocks, toxic chemicals, vibrations, or loud noise levels occasionally. However, reasonable accommodations are available to enable individuals with different abilities to perform effectively, ensuring a supportive and adaptable work setting. Your visual acuity, including close, distance, and color vision, will be essential in navigating through the diverse day-to-day demands of this position.

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