Top 30 Director of quality Jobs in Poway, Ca

Director, Quality Systems
Viking Therapeutics, Inc. —San Diego, CA
- $170,000 - $210,000 a year
- Writing skills
- Presentation skills
- Mentoring
Quick Apply
Director of Quality and Risk Management
Aurora San Diego —San Diego, CA
- $120,000 - $125,000 a year
- Management
- Hospital
- Master's degree
- Disability insurance
- Health insurance
Quick Apply
5d
Director of Quality and Population Health
DAP Health —El Cajon, CA
- $127,245 - $145,000 a year
- Weekends as needed
- Nursing
- Microsoft Access
- Word processing
Quick Apply
Associate Director, Quality Systems & Architecture
BD —San Diego, CA
- $169,800 - $280,300 a year
- 5 years
- Bachelor of Science
- Office
Sr Director, QMS
Dexcom —San Diego, CA
- $209,600 - $349,300 a year
- Full-time
- 11+ years
- Bachelor's degree
- Travel
Nursing Director of Quality Improvement & Population Health Management
TrueCare —San Marcos, CA
- $120,551 - $186,854 a year
- Full-time
- Nursing
- Patient care
- Bachelor of Science in Nursing
- Health insurance
- Dental insurance
Quick Apply
Director of Product Quality
Werfen —San Diego, CA
- $200,000 - $240,000 a year
- Online Application
- Bachelor of Science
- Engineering
- Analysis skills
Associate Director, Technical Operations Quality Control
Travere Therapeutics —San Diego, CA
- $150,000 - $195,000 a year
- Online Application
- Data analysis skills
- Master's degree
- 8 years
- Health insurance
- Paid time off
Quality Control Director
Argonaut Manufacturing Services —Carlsbad, CA
- $195,000 - $205,000 a year
- 8 hour shift
- Master's degree
- Analysis skills
- Bachelor's degree
- Health savings account
- Paid holidays
Quick Apply
Director, Quality Assurance - Technical
Travere Therapeutics —San Diego, CA
- $189,000 - $246,000 a year
- Online Application
- Master's degree
- Bachelor's degree
- Team management
- Health insurance
- Paid time off
13d
Sr. Director Quality Systems
BD —San Diego, CA
- $220,300 - $352,500 a year
- Bachelor of Science
- 11+ years
- Office
Associate Director, Development Quality Assurance
Ionis Pharmaceuticals, Inc. —Carlsbad, CA
- $154,500 - $196,873 a year
- Hybrid work
- 5 years
- Writing skills
- Master's degree
Quick Apply
Head of Quality & Regulatory Affairs - Autoimmunity
Werfen —San Diego, CA
- $240,000 - $280,000 a year
- Online Application
- HIPAA
- Bachelor's degree
- Travel
- Health insurance
- Dental insurance
7d
Associate Director, Quality Assurance - Technical
Travere Therapeutics —San Diego, CA
- $150,000 - $195,000 a year
- Online Application
- 8 years
- Bachelor's degree
- Travel
- Health insurance
- Paid time off
13d
Associate Director, Clinical Quality Assurance
Artiva Biotherapeutics —San Diego, CA
- $172,000 - $195,000 a year
- Full-time
- Remote
- Microsoft Word
- Microsoft Excel
- Management
- Paid holidays
- Disability insurance
Quick Apply
Sr. Director, Quality, Genetics Sciences Division (GSD)
Thermo Fisher Scientific —Carlsbad, CA
- $210,200 - $280,200 a year
- Full-time
- Engineering
- Office
- Analysis skills
- Commuter assistance
- Paid parental leave
2d
Senior Manager / Associate Director, GMP Quality Assurance Consultant
RegDev —San Diego, CA
- Office
- Master's degree
- Project management
Director, QC
PCI Pharma Services —San Diego, CA
- $151,360 - $170,280 a year
- Full-time
- 6 years
- Analysis skills
- Bachelor's degree
- Health insurance
- Dental insurance
Director, Customer Quality Engineering
Murata America —San Diego, CA
- $179,310.44 - $246,551.86 a year
- Ability to walk for extended periods
- Bachelor of Science
- Office
Sr/Exec Director, Quality Assurance GCP
Erasca —San Diego, CA
- $250,000 - $290,000 a year
- Remote
- 11+ years
- Bachelor's degree
- Mentoring
- Health savings account
- AD&D insurance
2d

I want to receive the latest job alert for director of quality in poway, ca

By signing in to your account, you agree to SimplyHired's Terms of Service and consent to our Cookie and Privacy Policy.

Explore jobs in more locations

director of quality jobs near poway, ca

Senior Director Of Quality Assurance jobs in San Diego, CA

Director Of Quality Assurance jobs in San Diego, CA

Regulatory Affairs Specialist jobs in San Diego, CA

Director Of Quality Assurance jobs in Carlsbad, CA

Director Of Quality jobs in San Diego, CA

Senior Director jobs in San Diego, CA

Senior Director Of Quality Assurance jobs in Holly Springs, NC

Senior Director Of Quality Assurance jobs in Marlborough, MA

Senior Director Of Quality Assurance jobs in Raleigh, NC

Quality Assurance Analyst jobs in Charlotte, NC

Senior Director Of Quality Assurance jobs in Bedford, MA

Legend Senior Living jobs in Lancaster, PA

Director Of Quality Assurance jobs in San Leandro, CA

Director Of Quality Assurance jobs in Chattanooga, TN

Pharmaceutical Quality Assurance jobs in Colorado

Director Of Quality Assurance jobs in Dallas, TX

Water Quality jobs in California

Director Of Quality Assurance jobs in Grand Rapids, MI

Hr Director jobs in New Jersey

Peer Support Specialist jobs in Connecticut

Director, Quality Systems

Viking Therapeutics, Inc.
San Diego, CA

Quick Apply

Job Details

$170,000 - $210,000 a year

Qualifications

Regulatory inspections
Stakeholder engagement
Team leadership
Writing skills
Compliance audits & assessments
Metrics Reporting
ICH Q9
Quality reports
Quality risk management
Quality assurance experience within pharmaceutical industry
Regulatory readiness in healthcare
Biomedical regulatory compliance
Management reporting
Quality audits
Audit support
Analytics

Full Job Description

Description:

The Director Quality Systems will lead and support quality assurance and quality systems activities for Viking’s clinical and commercial-stage operations. The role advances the company's Quality Management System, drives inspection readiness, and ensures quality processes are scalable, compliant, and aligned with late-stage development and commercial launch. The ideal candidate brings hands-on QA and Quality Systems experience, deep knowledge of GMP and FDA requirements, and a proven ability to partner cross-functionally to build a proactive, risk-based quality culture.

Essential Duties and Responsibilities

The main responsibilities of this role include:

Lead and manage the QS team, ensuring alignment with company objectives and regulatory standards
Develop, implement, and maintain quality management strategies and systems to ensure compliance with GMP, FDA, ICH guidelines, and other relevant regulatory bodies
Design, establish, and continuously improve the Quality Management System (QMS), including document control, change control, training systems, and electronic quality systems (eQMS) within Veeva.
Oversee the entire quality systems infrastructure, including Standard Operating Procedures (SOPs), Policies, batch records, specifications, testing, validation protocols and other GMP CMC documents.
Manage document lifecycle management ensuring version control, approval workflows, and archival in compliance with regulatory requirements
Establish and maintain quality metrics dashboards and Key Performance Indicators (KPIs) for system effectiveness
Establish and enforce quality assurance policies and procedures across all operational departments
Support the preparation and execution of internal audits, including regulatory inspections, to ensure compliance with regulatory requirements
Ensure timely resolution of quality-related issues, including non-conformances, deviations, and CAPA (Corrective and Preventive Actions)
Maintain inspection readiness and serve as primary QA point of contact for regulatory inspections
Collaborate with cross-functional teams (R&D, manufacturing, regulatory affairs, supply chain, etc.) to ensure product quality throughout the entire lifecycle
Partner with Regulatory Affairs to support CMC sections of regulatory submissions (IND, BLA, NDA)
Support technology transfer activities and new product introductions from a quality systems perspective
Lead continuous improvement initiatives leveraging methodologies to enhance product quality, manufacturing processes, and operational efficiency
Provide leadership in Quality Risk Management (QRM), including identification, assessment, and mitigation of quality risks using ICH Q9 principles
Prepare and present quality performance metrics, trending analysis, and reports to senior management and board of directors
Mentor and develop QS staff, fostering a culture of accountability, compliance, and continuous professional growth
Other duties as assigned.

Requirements:

Education and Experience

Bachelor's degree in Life Sciences, Engineering, or a related field
10+ years of progressive experience in Quality Assurance with at least 5 years in a leadership role within a regulated industry (pharmaceutical, biotechnology, or medical devices)

Knowledge and Skills

Strong knowledge of regulatory requirements, including FDA, GMP, ICH guidelines, ISO 13485, and 21 CFR Parts 210, 211, 600, 820, and 1271
Demonstrated expertise in Quality Management Systems (QMS) design, implementation, and maintenance
Proven experience with electronic quality systems (eQMS) platforms such as Veeva
Knowledge of Quality Risk Management methodologies (ICH Q9, FMEA, etc.)
Demonstrated ability to drive process improvements and manage complex quality systems in dynamic environments
Experience managing regulatory inspections and audit readiness programs
Excellent problem-solving, analytical, and decision-making skills
Strong written and verbal communication skills, with the ability to interact with senior leadership, regulatory agencies, and external stakeholders
Experience in preparing and presenting reports and metrics to senior management and board members
Strong leadership and interpersonal skills, with the ability to mentor and guide teams towards excellence
Ability to work effectively in a fast-paced, entrepreneurial environment with changing priorities

VIKING THERAPEUTICS

Viking Therapeutics, Inc., is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status. Viking Therapeutics also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as work authorization and employment eligibility verification requirements of the Immigration and Nationality Act and IRCA.

Notice to Agency and Search Firm Representatives

Viking Therapeutics, Inc. is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Viking employee by a third-party agency and/or search firm without a valid written & signed search agreement, and assignment of specific position, will become the sole property of Viking Therapeutics, Inc. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral.

Salary Description

$170,000.00 - $210,000.00 annual salary

Quick Apply

Refine Your Search

director of quality jobs in poway, ca

Director, Quality Systems

Director of Quality and Risk Management

Director of Quality and Population Health

Associate Director, Quality Systems & Architecture

Sr Director, QMS

Nursing Director of Quality Improvement & Population Health Management

Director of Product Quality

Associate Director, Technical Operations Quality Control

Quality Control Director

Director, Quality Assurance - Technical

Sr. Director Quality Systems

Associate Director, Development Quality Assurance

Head of Quality & Regulatory Affairs - Autoimmunity

Associate Director, Quality Assurance - Technical

Associate Director, Clinical Quality Assurance

Sr. Director, Quality, Genetics Sciences Division (GSD)

Senior Manager / Associate Director, GMP Quality Assurance Consultant

Director, QC

Director, Customer Quality Engineering

Sr/Exec Director, Quality Assurance GCP

I want to receive the latest job alert for director of quality in poway, ca

Related Searches

Explore jobs in more locations

Job Seeker Tools

Employer Tools

Browse

Stay Connected