Top 523 Director, revenue cycle management Jobs in Oceanside, Ca

Head of Quality
Gallant —San Diego, CA
- From $175,000 a year
- Weekends as needed
- Background check
- Master's degree
- 8 years
- Health insurance
- Dental insurance
Quick Apply
Regional Sales Director, Channel Sales
Semrush Inc. —California
- $250,500 - $303,000 a year
- Full-time
- Remote
- Travel
- Senior level
- Paid parental leave
- Parental leave
Director of Sales & Marketing
Advontemedia Inc. —Temecula, CA
- $75,000 - $120,000 a year
- Full-time
- Background check
- Management
- 5 years
- Health insurance
- Vision insurance
Quick Apply
6d
Fractional Real Estate Controller/Director of Finance & Capital Planning
Confidential —Carlsbad, CA
- $125 - $175 an hour
- Part-time
- Hybrid work
- Microsoft Excel
- CPA
- Office
Quick Apply
3d
Director, Oncology Customer Experience Operations
Hologic —San Diego, CA
- $151,200 - $268,800 a year
- Full-time
- Management
- HIPAA
- Bachelor's degree
Robotic Solution Director
Kellermeyer Bergensons Services —Oceanside, CA
- $160,000 - $170,000 a year
- Monday to Friday
- Office
- Analysis skills
- Bachelor's degree
Quick Apply
Executive Director Head of Global Regulatory Strategy
EPM Scientific —Carlsbad, CA
- $250,000 - $320,000 a year
- Bachelor's degree
- Mentoring
- Senior level
Quick Apply
14d
DIS TECH - US Sales Lead / Account Manager (Flexible Level)
DIS Tech —San Diego, CA
- From $135,000 a year
- Full-time
- Hybrid work
- Engineering
- 3 years
- Travel
- Health insurance
- Dental insurance
Quick Apply
Associate Director of Toxicology
Kelly Services —Carlsbad, CA
- $175,000 - $250,000 a year
- Full-time
- Master's degree
- Doctor of Philosophy
- Neurology
- Paid holidays
- Disability insurance
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AR Specialist 2
Rancho Health MSO, Inc —Temecula, CA
- $24 - $28 an hour
- Full-time
- Writing skills
- Mid-level
- 3 years
Quick Apply
Revenue Cycle Billing & Coding
Rancho Health MSO, Inc —Temecula, CA
- $24 - $28 an hour
- Full-time
- Hybrid work
- Mid-level
- Office
- High school diploma or GED
Quick Apply
Director of Admissions
Fusion Academy —San Diego, CA
- $68,000 - $78,000 a year
- Full-time
- Background check
- Marketing
- Business development
- Commuter assistance
- Paid holidays
Maintenance Director
Gateway Park Senior Living —Poway, CA
- $27 - $30 an hour
- Full-time
- Background check
- Writing skills
- Basic math
- Paid holidays
- Health insurance
Quick Apply
12h
Physical Therapist - Clinic Director
Spine & Sport Physical Therapy —Encinitas, CA
- $95,000 - $130,000 a year
- Full-time
- CPR Certification
- Doctoral degree
- BLS Certification
- Loan repayment program
- Health insurance
Quick Apply
Resident Service Director (LVN or RN required)
Alta Vista Senior Living —Vista, CA
- $71,000 - $73,000 a year
- Full-time
- Background check
- CPR Certification
- LVN
- Paid holidays
- Health insurance
Quick Apply
6d
Strategic Pursuits Director - West Agency
RailPros —California
- $150,000 - $175,000 a year
- Full-time
- Remote
- 5 years
- Analysis skills
- Senior level
- Commuter assistance
- Health savings account
Quick Apply
7d
Private Client Director, Alpha - $200,000/year USD
Crossover —La Jolla, CA
- Full-time
- School experience
- US work authorization
- In-person
- Relocation assistance
Quick Apply
Director of Community Impact
San Diego Food Bank —San Diego, CA
- $100,000 - $120,000 a year
- Full-time
- Supervising experience
- Mentoring
- Senior level
Quick Apply
Director of Rehab
Powerback Rehabilitation —California
- $58 - $65 an hour
- Full-time
- Master's degree
- Bachelor's degree
- Senior level
- Relocation assistance
- Health insurance
Medical Director (Med Spa / Aesthetics) – Remote (California)
SWELL Medical —California
- Part-time
- Remote
- Medicine
- Management
- Mid-level
- Professional development assistance
- Flexible schedule
Quick Apply

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Head of Quality

Gallant
San Diego, CA

Quick Apply

Job Details

Full-time
From $175,000 a year

Benefits

Health insurance
Dental insurance
401(k)
Paid time off
Vision insurance
401(k) matching
Life insurance

Qualifications

Biology
Biotechnology
Teamwork
Team leadership
Drug regulation
GMP
Cleanroom protocols
ICH Q9
Master's degree
Manufacturing facility experience
Bachelor's degree
Pharmaceutical company experience
Quality assurance experience within pharmaceutical industry
Regulatory/legal compliance standards in production
Cleanroom experience
Biomedical regulatory compliance
Quality control experience within pharmaceutical industry
Sterile products production
Managing product quality assurance teams
Cross-functional communication
Senior leadership
Pharmaceutical manufacturing facility experience

Full Job Description

Position Summary

Director, Head of Quality to establish and lead all Quality Assurance (QA) and Quality Control (QC) activities for our pet-specific cell and gene therapy programs. Reporting directly to the CEO, this Director-level role will design and maintain a phase-appropriate, risk-based Quality Management System (QMS) that ensures full compliance with current Good Manufacturing Practices (cGMP) and applicable veterinary regulatory requirements. The ideal candidate will bring deep expertise in aseptic processing and sterile product manufacturing, combined with a pragmatic, risk-based approach suitable for both early clinical and late-stage commercial readiness. This is a critical leadership position that will shape quality culture and enable rapid, compliant advancement of our novel therapies for pets.

Key Responsibilities

Develop, implement, and continuously improve a phase-appropriate QMS tailored to cell and gene therapy manufacturing, applying risk-based principles (per ICH Q9 and FDA guidance) across process development, clinical supply, and commercial-scale production.
Provide strategic and operational leadership for all QA/QC functions, including batch record review, product release, deviation investigations, CAPA management, change control, and stability programs.
Oversee aseptic process validation, environmental monitoring, media fill programs, and sterility assurance for cell and viral-vector manufacturing in ISO-classified cleanrooms.
Ensure timely and compliant support for regulatory submissions (e.g., FDA Center for Veterinary Medicine (CVM) Investigational New Animal Drug (INAD) applications and eventual New Animal Drug Applications (NADA)).
Conduct and manage internal audits, supplier/CMO quality oversight, and preparation for regulatory inspections (FDA CVM, USDA APHIS if applicable).
Collaborate cross-functionally with Manufacturing, Process Development, Regulatory Affairs, and Clinical teams to integrate quality into every stage of product lifecycle.
Build, mentor, and lead a high-performing Quality team; establish quality metrics, training programs, and a culture of continuous improvement.
Perform risk assessments and implement mitigation strategies for manufacturing, testing, and distribution activities.
Stay current with evolving FDA CVM, USDA, and international guidelines specific to veterinary advanced therapies.

Required Qualifications

Education

Bachelor’s or Master’s degree in a scientific discipline (Biology, Microbiology, Chemistry, Chemical Engineering, or related field) required. PhD is not necessary.

Experience

Minimum 8–10 years of progressive Quality experience in the biopharmaceutical industry, with at least 5 years focused on cell therapy, gene therapy, or complex biologics manufacturing.
Demonstrated success leading or significantly contributing to phase-appropriate, risk-based quality systems in GMP environments (early development through commercialization).
Hands-on or direct oversight experience in aseptic processing, sterile product manufacturing, cleanroom operations, and sterility assurance programs.
Proven track record managing QA/QC for autologous or allogeneic cell products and/or viral-vector gene therapies.
Prior experience at the Manager or Director level with direct reports and cross-functional influence.

Skills & Competencies

Thorough working knowledge of U.S. GMP regulations (21 CFR Parts 210/211, 600 series, and veterinary-specific guidance from FDA CVM), ICH guidelines, and risk-management principles.
Strong analytical, problem-solving, and decision-making skills with the ability to balance speed and compliance in a fast-paced biotech setting.
Excellent written and verbal communication; able to represent Quality in regulatory interactions and internal leadership forums.
Passion for animal health and a collaborative, pragmatic leadership style.

Preferred Qualifications

Direct experience with veterinary biologics or FDA CVM-regulated products.
Previous work in a startup or small-biotech environment.
Professional certifications (e.g., ASQ CQA, CQE, or sterile manufacturing/aseptic processing training) are advantageous but not required.

Location & Work Environment

This is a full-time, on-site position based at our cGMP manufacturing facility. The role requires hands-on presence on the manufacturing floor during production campaigns, including occasional off-shift or weekend support as dictated by the manufacturing schedule.

All duties will be performed in strict compliance with FDA regulations related to the manufacture of cell and gene therapy products for veterinary medicine, including current Good Manufacturing Practice (cGMP) and CVM-specific guidance. The Director of Quality plays a critical role in ensuring the safe, compliant, and reliable production of advanced veterinary therapies.

We are an equal opportunity employer committed to advancing safe and effective veterinary cell and gene therapies in full accordance with FDA/CVM standards.

ABOUT GALLANT

Gallant is the leader in veterinary regenerative medicine on a mission to bring transformational “ready-to-use” stem cell therapies to pets everywhere that treat the root cause of disease. With five high value clinical stage programs in development and a platform that is generating additional therapies, the company is positioned for their first FDA conditional approval in 2026, bringing a new class of therapies to animal health.

Gallant is a privately-held company and backed by top venture capital firms BOLD Capital, Digitalis Ventures, Hill Creek Partners and NovaQuest, and recently completed our Series B financing. We have onsite GMP manufacturing, R&D and offices headquartered in La Jolla, CA.

We offer a competitive base salary, generous health benefits, stock compensation, PTO, pet-friendly offices, and a virtual work environment as needed. We are a tight, incredibly smart and passionate team, deeply committed to our vision to bring “ready-to-use” stem cell therapies to pets worldwide.

Pay: From $175,000.00 per year

Benefits:

401(k)
401(k) matching
Dental insurance
Health insurance
Life insurance
Paid time off
Vision insurance

Application Question(s):

Can you tell us why you would be a good fit for this role?

Experience:

Quality experience in the biopharmaceutical industry: 8 years (Required)

Work Location: In person

Quick Apply

Refine Your Search

director, revenue cycle management jobs in oceanside, ca

Head of Quality

Regional Sales Director, Channel Sales

Director of Sales & Marketing

Fractional Real Estate Controller/Director of Finance & Capital Planning

Director, Oncology Customer Experience Operations

Robotic Solution Director

Executive Director Head of Global Regulatory Strategy

DIS TECH - US Sales Lead / Account Manager (Flexible Level)

Associate Director of Toxicology

AR Specialist 2

Revenue Cycle Billing & Coding

Director of Admissions

Maintenance Director

Physical Therapist - Clinic Director

Resident Service Director (LVN or RN required)

Strategic Pursuits Director - West Agency

Private Client Director, Alpha - $200,000/year USD

Director of Community Impact

Director of Rehab

Medical Director (Med Spa / Aesthetics) – Remote (California)

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