Top 289 Quality manager Jobs in Vernon Ca

Senior Manager, Quality Systems
Hims & Hers —Los Alamitos, CA
- $150,000 - $180,000 a year
- Full-time
- Remote
- 7 years
- System design
- Mentoring
- Employee stock purchase plan
- Health insurance
Quality Manager
Industrial Parts Depot —Carson, CA
- $125,000 - $140,000 a year
- Full-time
- Management
- Analysis skills
- Bachelor's degree
- Health insurance
- Dental insurance
Quick Apply
Quality Improvement & Data Analytics Manager
Family Health Matters —Anaheim, CA
- $72,000 - $80,000 a year
- Full-time
- Background check
- Mid-level
- Bachelor's degree
- Health insurance
- Dental insurance
Quick Apply
Director of Quality
Watts Healthcare Corporation —Los Angeles, CA
- $120,165.72 - $144,715.70 a year
- Full-time
- Ability to walk for extended periods
- Office
- Bachelor's degree
- Health insurance
- Dental insurance
Quick Apply
Quality Control Supervisor
GuruNanda LLC —Buena Park, CA
- Up to $75,000 a year
- Full-time
- Background check
- Microsoft Excel
- Microsoft Access
- Health insurance
- Dental insurance
Quick Apply
Quality Control Supervisor
CalPortland —Irwindale, CA
- $75,000 - $100,000 a year
- Background check
- Microsoft Excel
- Microsoft Outlook
- Disability insurance
- Health insurance
Director Quality and Performance Excellence
Community Hospital of Huntington Park —Huntington Park, CA
- $139,588.80 - $205,233.60 a year
- Hospital
- Customer service
- 5 years
Quick Apply
Inspection Supervisor
[email protected] —Santa Fe Springs, CA
- $35 - $55 an hour
- Extended hours
- Spanish
- Schematics
- Mid-level
- Paid holidays
- Health insurance
Quick Apply
Manager, Quality Control
VACCO Industries —South El Monte, CA
- $92,262 - $127,995 a year
- Full-time
- Management
- Writing skills
- Microsoft Office
- Health savings account
- Health insurance
Quick Apply
AEROSPACE SUPERVISOR QUALITY CONTROL
Marvin Engineering Co. —Inglewood, CA
- $28.85 - $36.35 an hour
- Online Application
- 5 years
- Computer literacy
- Basic math
Quick Apply
Quality Manager - Hawthorne, CA
Leapros Professional —Hawthorne, CA
- $110,000 - $120,000 a year
- Call employer
- Management
- 5 years
- Engineering
Quick Apply
Quality Assurance Manager
Fit-Line Global —Brea, CA
- $100,000 a year
- Full-time
- Spanish
- Microsoft Excel
- Management
- Health savings account
- Paid holidays
Quick Apply
Final Lab Technician Quality Lead - 1st Shift
Howmet Aerospace —Carson, CA
- $35 - $42 an hour
- Full-time
- 5 years
- English
- High school diploma or GED
- Paid holidays
- Health insurance
Quick Apply
Quality Assurance Manager
Fit-Line Global —Brea, CA
- $100,000 a year
- Full-time
- Spanish
- Microsoft Excel
- Management
- Health savings account
- Paid holidays
Quick Apply
Air Quality Manager
SA Recycling LLC —Orange, CA
- $110,000 - $130,000 a year
- Background check
- Spanish
- Management
Quick Apply
Manager Lab Services (Quality) QA/QM
Martin Luther King, Jr. Community Hospital —Los Angeles, CA
- Full-time
- Hospital
- Bachelor of Science
- Bachelor's degree
16h
Quality Manager – Aerospace & Defense Manufacturing
Gear Manufacturing Inc. —Anaheim, CA
- From $90,000 a year
- Full-time
- Background check
- Management
- 5 years
- Paid holidays
- Health insurance
Quick Apply
Sr. Regional Operations Manager - Central/Northern California
OPENLANE —Los Angeles, CA
- $95,000 - $100,000 a year
- Full-time
- Remote
- Customer service
- Driver's License
- Travel
- Paid parental leave
- Health savings account
Quick Apply
14d
Regional Operations Manager - San Fernando, CA
OPENLANE —San Fernando, CA
- $80,000 a year
- Full-time
- Remote
- Mid-level
- Driver's License
- Continuous improvement
- Paid parental leave
- Health savings account
Quick Apply
14d
Quality Manager (Manufacturing Preferred)
Leoforce —Buena Park, CA
- $150,000 a year
- Engineering
- Mentoring
- Senior level
- Paid training
- Health insurance
Quick Apply

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Senior Manager, Quality Systems

Hims & Hers -
Los Alamitos, CA

Apply Now

Job Details

Full-time
$150,000 - $180,000 a year

Benefits

Employee stock purchase plan
Health insurance
Unlimited paid time off
Dental insurance
Parental leave
Vision insurance
401(k) matching

Qualifications

Content creation for technical audiences
Defect resolution root cause analysis
Team supervision
Document control experience within pharmaceutical industry
Coaching
Technical writing experience within manufacturing
Compliance audits & assessments
Corrective and preventive actions (CAPA)
Quality control audit
Change management
Team development
ICH guidelines
Quality risk management
Mentoring
Leading team collaboration initiatives
Operational excellence initiatives
Quality audits
Process improvement planning
Root cause analysis
Cross-functional team management
Cross-functional communication
Audit support
Pharmaceutical manufacturing facility experience

Full Job Description

Hims & Hers is the leading health and wellness platform, on a mission to help the world feel great through the power of better health. We are redefining healthcare by putting the customer first and delivering access to care that is affordable, accessible, and personal, from diagnosis to treatment to delivery. No two people are the same, so we provide access to personalized care designed for results. By normalizing health & wellness challenges and innovating on their solutions, we’re making better health outcomes easier to achieve.

Hims & Hers is a public company, traded on the NYSE under the ticker symbol “HIMS.” To learn more about the brand and offerings, you can visit hims.com/about and hims.com/how-it-works . For information on the company’s outstanding benefits, culture, and its talent-first flexible/remote work approach, see below and visit www.hims.com/careers-professionals.

About the Role:

The Sr. Manager, Quality Systems serves as the subject matter expert (SME) and owner of the site Quality Management System (QMS) within a sterile cGMP manufacturing environment. This role is responsible for designing, establishing, maintaining, and continuously improving the QMS framework — including Document Control and Data Integrity, Change Control, Deviations and CAPA, Training, Internal Audit, and Management Review — in alignment with FDA cGMP (21 CFR 210/211/11), Section 503B, and other applicable standards.

The successful candidate will bring deep Quality Systems expertise, a builder’s mindset, and a proven track record of strengthening compliant, audit-ready systems in sterile pharmaceutical operations. This individual will be central to ensuring inspection readiness, regulatory compliance, and a culture of continuous improvement across the site.

This role will begin as an individual contributor and site SME for Quality Systems, with the opportunity to build and lead a team as the QMS and the organization mature.

You Will:

Lead the design, implementation, and continuous improvement of the site QMS, ensuring compliance with cGMP, 503B, and applicable global standards and best practices.
Implement and administer the site electronic QMS (TrackWise), in conjunction with global process owners, including data migration, training, and development of site processes/procedures.
Develop, monitor, and report quality metrics and KPIs to site and senior leadership; lead Management Review and drive data-driven decision-making.
Own the document control system for all GMP documentation (SOPs, work instructions, forms, policies), ensuring records are current, reviewed, approved, controlled, and distributed. Interface with global stakeholders and process owners to review and integrate business-unit and global policies at the site.
Maintain a secure, compliant repository and ensure document retention and archival align with regulatory and company requirements.
Champion data integrity (ALCOA+) and compliance with 21 CFR Part 11 across paper and electronic records.
Own the Deviation and CAPA programs, coaching/mentoring owners, approving records, and ensuring timely investigation, sound root cause analysis, and effective closure.
Own the Change Control program, driving effective planning, risk-based guidance across cross-functional teams, SME assessments, tracking implementation, and on-time closure.
Establishing governance processes for relevant Quality System elements, to enhance oversight and drive accountability.
Develop, implement, and maintain the site training/competency program and Learning Management System (LMS), ensuring GMP and role-based training matrix compliance for all personnel.
Conduct training assessments, develop training materials, and coordinate onboarding, recurring, specialized, and trend-driven retraining; maintain accurate, audit-ready training records.
Establish and lead the internal audit program and maintain a state of continuous inspection readiness.
Support FDA, state board, and global audits; coordinate and author responses to observations (e.g., Form 483) and drive corrective actions to completion.
Own investigations, change controls, assessments, projects, and other records for areas of responsibility.
Partner with Manufacturing, Quality, R&D, Engineering, Regulatory, and site leadership to resolve quality issues and foster a culture of compliance and accountability.
Maintain current expertise in regulations and guidance (FDA, ICH, etc.), regulatory intelligence & industry trends, and implementing changes as needed.

You Have:

Bachelor’s degree in Life Sciences, Engineering, Quality, or a related field (or equivalent experience).
7+ years of progressive experience in Quality Assurance / Quality Systems within an FDA-regulated environment; sterile injectable cGMP or 503B experience strongly preferred.
Demonstrated ownership of multiple QMS elements (document control, change control, deviations, CAPA, training, audit). Experience building and/or remediating systems in a high-growth environment preferred.
Proven ability to lead teams, drive continuous improvement, and develop strategies that result in measurable quality enhancements.
Hands-on experience in paper systems and implementing and administering an eQMS (e.g. TrackWise).
Deep, working knowledge of industry regulations and guidance (FDA, ISO, ICH, EMA).
Experience supporting regulatory (i.e. FDA) inspections and audits in front or back room with successful outcomes.
Strong background in root cause analysis, risk management, and continuous improvement methodologies.
Experience leading, mentoring, or developing others, with the ability to build and lead a team as the role scope grows.
Experience interfacing with Senior Leadership, inclusive of effective delivery of metrics, remediation plans, etc.
Excellent technical writing, communication, and cross-functional collaboration skills.
Demonstrated ability to independently prioritize, problem-solve, and deliver results in a fast-paced environment, with minimal supervision and high accountability.

Our Benefits (there are more but here are some highlights):

Competitive salary & equity compensation for full-time roles
Unlimited PTO, company holidays, and quarterly mental health days
Comprehensive health benefits including medical, dental & vision, and parental leave
Employee Stock Purchase Program (ESPP)
401k benefits with employer matching contribution
Offsite team retreats

We are committed to building a workforce that reflects diverse perspectives and prioritizes ethics, wellness, and a strong sense of belonging. If you're excited about this role, we encourage you to apply—even if you're not sure if your background or experience is a perfect match.

Hims considers all qualified applicants for employment, including applicants with arrest or conviction records, in accordance with the San Francisco Fair Chance Ordinance, the Los Angeles County Fair Chance Ordinance, the California Fair Chance Act, and any similar state or local fair chance laws.

It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

Hims & Hers is committed to providing reasonable accommodations for qualified individuals with disabilities and disabled veterans in our job application procedures. If you need assistance or an accommodation due to a disability, please contact us at [email protected] and describe the needed accommodation. Your privacy is important to us, and any information you share will only be used for the legitimate purpose of considering your request for accommodation. Hims & Hers gives consideration to all qualified applicants without regard to any protected status, including disability. Please do not send resumes to this email address.

To learn more about how we collect, use, retain, and disclose Personal Information, please visit our Global Candidate Privacy Statement.

Compensation Range: $150K - $180K

Apply Now

Refine Your Search

quality manager jobs in vernon ca

Senior Manager, Quality Systems

Quality Manager

Quality Improvement & Data Analytics Manager

Director of Quality

Quality Control Supervisor

Quality Control Supervisor

Director Quality and Performance Excellence

Inspection Supervisor

Manager, Quality Control

AEROSPACE SUPERVISOR QUALITY CONTROL

Quality Manager - Hawthorne, CA

Quality Assurance Manager

Final Lab Technician Quality Lead - 1st Shift

Quality Assurance Manager

Air Quality Manager

Manager Lab Services (Quality) QA/QM

Quality Manager – Aerospace & Defense Manufacturing

Sr. Regional Operations Manager - Central/Northern California

Regional Operations Manager - San Fernando, CA

Quality Manager (Manufacturing Preferred)

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