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Manager, Supplier Development and Quality
Castelion
Quality engineer job in Torrance, CA
Castelion is bringing a new approach to defense development and production: one that focuses on short, iterative design cycles, rapid testing in development, and modern commercial manufacturing strategies for production at scale. We're designing, building, and testing next generation long range strike weapons systems to give America and its Allies a definitive edge and deter future conflicts.
Manager, Supplier Development and Quality
As the Manager of Supplier Development and Quality, you will play a critical role in partnering with cross-functional teams to define, develop, qualify, and sustain the supplier base supporting Castelion vehicle and missile subsystems. This role requires an experienced quality and supplier development leader who can work closely with engineering, manufacturing, and supply chain to ensure suppliers meet technical, quality, and delivery requirements throughout development and production. You will lead supplier qualifications, audits, performance management, and continuous improvement initiatives to align near-term development schedules with long-term quality, reliability, and scalability objectives. We seek intelligent, collaborative, and driven leaders who are passionate about building robust supplier partnerships and quality systems from the ground up. If you thrive in fast-paced, high-accountability environments and are motivated by making a tangible impact on mission-critical hardware, we want to hear from you.
Responsibilities
Lead supplier development activities in collaboration with engineering, manufacturing, and strategic sourcing to ensure suppliers are capable of meeting quality, technical, and schedule requirements for development and production programs.
Evaluate, qualify, and approve suppliers based on quality systems, technical capability, reliability, risk, and cost, building a resilient and scalable supplier base to support Castelion's rapid development and production cadence.
Define and manage supplier quality requirements, including audits, qualifications, AS9102 FAIRs, certifications, and ongoing compliance to aerospace and company standards.
Collaborate with cross-functional stakeholders to drive supplier performance improvements in quality, delivery, cost, and service while identifying and mitigating supply chain and compliance risks.
Support contract reviews and negotiations by ensuring quality, technical, and regulatory requirements are clearly defined, achievable, and enforceable with suppliers.
Facilitate design-for-manufacturability and design-for-quality reviews with engineering and suppliers to proactively reduce risk and improve producibility.
Partner with engineering and operations to address nonconforming material, supplier escapes, and rejected hardware through root cause analysis and corrective action, with a focus on prevention and continuous improvement.
Establish and maintain supplier performance metrics, reporting regularly to stakeholders on quality trends, risks, and critical issues.
Build and maintain strong supplier relationships through regular engagement, performance reviews, and development plans.
Ensure supplier compliance with company policies, quality management systems, and applicable customer, industry, and government regulations.
Basic Qualifications
Educational Background: Bachelor's degree or equivalent
Technical Proficiency: 6+ years of experience working in a related field, program, or project
Preferred Skills and Experience
Aerospace Quality Systems: Experience operating within AS9100-compliant environments, including supplier qualification, audits, AS9102 FAIRs, corrective actions, and ongoing supplier compliance.
Manufacturing & Technical Expertise: Broad knowledge of aerospace manufacturing processes and suppliers, including machined parts, composites, chemicals, and avionics and their relevant specifications, typical customer requirements, and certifications.
Supplier Development & Analytics: Strong root cause and corrective action capability using structured problem-solving methods (e.g., 8D, Six Sigma, Lean), supported by data-driven analysis in Excel, SQL, or similar tools.
Business & Quality Systems: Familiarity with ERP, MRP, and Quality Management Systems to manage supplier data, nonconformances, and documentation accuracy.
Security Clearance: Active U.S. Government security clearance or the ability to obtain one.
All employees are granted long-term stock incentives as part of their employment at Castelion. All employees receive access to comprehensive medical, vision, and dental insurance, and the company offers four weeks of paid time off per year.
Leadership Qualities
Bias to Action and Creative Problem Solving. Desire and experience questioning assumptions in ways that lead to break through ideas that are ultimately implemented. Successfully bring in applicable processes/concepts/materials from other industries to achieve efficiency gains. Ability to personally resolve minor issues in development without requiring significant support.
High Commitment, High Initiative. A successful candidate will have a genuine passion for Castelion's mission and consistently look for ways to contribute to the company's technical goals and prevent hardware blockers. Ability to work in a fast paced, autonomously driven, and demanding atmosphere. Strong sense of accountability and integrity.
Clear Communicator. Proactively communicates blockers. Trusted in previous roles to be voice of company with regulators, suppliers, gate keepers and customers. Capable of tactfully managing relationships with stakeholders to achieve company-desired outcomes without compromising relationships. Emails, IMs and verbal interactions are logical, drive clarity, and detailed enough to eliminate ambiguity.
ITAR Requirements:
To conform to U.S. Government export regulations, applicant must be a (i) U.S. citizen or national, (ii) U.S. lawful, permanent resident (aka green card holder), (iii) Refugee under 8 U.S.C. § 1157, or (iv) Asylee under 8 U.S.C. § 1158, or be eligible to obtain the required authorizations from the U.S. Department of State.
Employment with Castelion is governed on the basis of competence and qualifications and will not be influenced in any manner by race, color, religion, gender, national origin/ethnicity, veteran status, disability status, age, sexual orientation, gender identity, marital status, mental or physical disability or any other legally protected status.
$117k-176k yearly est. 2d ago
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Quality Assurance Manager
Ingersoll Rand 4.8
Quality engineer job in Burbank, CA
The ideal candidate is a critical thinker who will proactively improve the quality systems of the company through internal audits, participation in process improvement programs, and interaction with key partners to obtain constructive feedback.
Responsibilities
Develop standardized production, quality, and customer-service standards
Identify potential risks before they become a problem, focusing on root cause analysis and preventive action
Perform internal and external quality audits and compile detailed reports of findings
Build a strong team through coaching, mentoring, specific training and performance evaluations
Qualifications
Bachelor's degree or equivalent experience in Engineering
10+ years' relevant work experience
Experience managing or leading teams
Highly organized with excellent attention to detail
$115k-143k yearly est. 2d ago
Quality Assurance Manager
Astrix 4.1
Quality engineer job in Anaheim, CA
Company Overview: Our client is a well-established specialty ingredient manufacturer serving the food and beverage industry. With a focus on innovation and quality excellence, they produce high-value color solutions and sweet ingredient systems for leading brands nationwide.
Location: Onsite in Anaheim, CA
Compensation: $80,000-$100,000k/year
Type: Direct-hire
Hours: M-F 8-5
Essential Duties:
Direct and oversee all quality assurance functions to maintain product safety, quality standards, and regulatory adherence throughout daily operations.
Manage the resolution of quality deviations, investigate customer feedback issues, and implement corrective and preventive measures.
Oversee quality control activities including inspection protocols, sample analysis, testing procedures, and approval processes for incoming materials, in-process production, and final products.
Maintain and enhance food safety management systems encompassing allergen management, sanitation verification, product traceability, and vendor approval programs.
Execute internal compliance assessments and provide support during regulatory inspections and third-party certification audits.
Develop and deliver training programs for quality personnel and manufacturing teams on quality systems and food safety requirements.
Manage quality records and documentation systems including production records, certificates of analysis, and deviation documentation.
Contribute to technical specification creation and updates for both new product launches and existing product portfolios, with emphasis on specialty color and confectionery ingredient applications.
Required Qualifications:
Bachelor's degree in Food Science, Industrial Microbiology, Chemistry, or closely related scientific discipline strongly preferred.
Minimum 3 years of progressive quality assurance experience within food processing or ingredient manufacturing operations.
Comprehensive understanding of FDA regulatory framework, HACCP methodology, GMP requirements, and Global Food Safety Initiative standards (such as SQF or BRC certification schemes).
Demonstrated capability in root cause investigation techniques and corrective/preventive action system management.
Strong supervisory capabilities with excellent verbal and written communication skills and organizational abilities.
Proven ability to excel in a high-paced, collaborative production environment while maintaining meticulous attention to detail.
HACCP certification or PCQI (Preventive Controls Qualified Individual) credential.
SQF Practitioner or BRC auditor training.
This job description is a complete list of all desired skills, but not all are required. We strongly encourage candidates who have some of the skills to apply. We look forward to a conversation to learn more about you!
$92k-140k yearly est. 1d ago
Supervisor , Continuous Quality Monitoring
Regal Medical Group 3.8
Quality engineer job in Los Angeles, CA
The CQM Supervisor oversees non-clinical auditors in the Clinical Quality Management (CQM) department, ensuring regulatory compliance and the quality of processes in daily Non-Clinical Utilization Management (UM) activities, under the direction of a manager. This Supervisor is responsible for conducting live audits of UM case files, assigning drivers and presenters, and ensuring their performance is appropriate. The role also involves monitoring UM system controls and processes, specifically those that do not require clinical decisions. A solid understanding of comprehensive regulations, UM policies and procedures, the UM system, UM auditing, and quality improvement is essential for this position.
Essential Duties and Responsibilities:
- Familiarity with Non-Clinical UM regulations, processes, and systems.
- Ability to assign workloads effectively while managing staff.
- Proficient in presenting case files and conducting interviews regarding non-clinical questions.
- Skilled in designing audit tools to monitor Non-Clinical UM processes completed by non-clinical staff.
- Strong communication skills for effective interaction with internal clients and external customers.
- Capable of training employees using Policies & Procedures (P&Ps) and audit tools.
- Provide constructive feedback and exhibit strong active communication skills.
- Summarize quality monitoring findings, analyze root causes, and propose quality improvement plans.
- Suggest and design focused audits that help improve compliance in Non-Clinical UM processes.
- Request decision support for creating and enhancing Non-Clinical UM monitoring reports based on changes to UM P&Ps.
- Ensure auditors complete audits and necessary remediation within specified timeframes.
- Collaborate with the Non-Clinical UM team to ensure monitored focus areas are addressed and that process quality is tracked.
- Work with operational teams to evaluate the effectiveness and efficiency of process changes made for quality improvement.
- Ensure that new processes are accurately implemented through reports and case file reviews.
- Report issues identified to the Prior Authorization Compliance Director based on findings.
- Review updated policies and procedures, and be able to update the quality monitoring tool accordingly.
- Maintain all evidence related to quality monitoring projects.
- Track and manage daily reports received from the decision support team.
- Report any issues related to internal processes (e.g., timeliness) to the CQM manager.
- Attend department meetings, in-house services, and trainings, completing acknowledgments within the required timeframe.
- Perform all other duties as directed by management.
Education and Experience:
- Three to five (3-5) years of experience in non-clinical utilization management.
- Preferred: at least two (2) years of experience in non-clinical UM supervision or auditing.
- Proficiency in MS Office programs (Word, Excel, Outlook, Access, PowerPoint).
- Typing speed of 60 words per minute with accuracy.
- Ability to handle confidential matters responsibly.
- Strong analytical, creative problem-solving, and organizational skills.
- Capacity to work in a multi-tasking, high-stress environment.
- Effective strategy execution within timelines, delivering quality results.
- Ability to adapt and thrive in a fast-paced environment, demonstrating proactivity.
- Capable of managing multiple projects simultaneously, adjusting priorities daily, and knowing when to seek assistance with conflicting priorities.
- Self-motivated, assertive, ambitious, and possessing high personal ethics.
- Ability to collaborate with all levels of management and establish positive working relationships across various divisions in the company.
Compensation:
The pay range for this position at the start of employment is expected to be between $70,304 and $72,000 annually, depending on experience. However, the base pay offered may vary based on multiple individual factors, including market location, job-related knowledge, licensure, skills, and overall experience.
The total compensation package for this position may also include other elements, such as a sign-on bonus and discretionary awards, along with a full range of medical, financial, and other benefits (including 401(k) eligibility and various paid time off benefits, such as vacation, sick time, and parental leave), depending on the position offered.
Details regarding participation in these benefit plans will be provided to employees who receive an employment offer. If hired, the employee will be in an “at-will position,” and the company reserves the right to modify base salary (along with any other discretionary payments or compensation programs) at any time, including for reasons related to individual performance, overall company performance, or market factors.
As one of the fastest-growing Independent Physician Associations in Southern California, Regal Medical Group, Lakeside Community Healthcare, and Affiliated Doctors of Orange County offer a dynamic and fast-paced work environment.
Employer will consider for employment qualified applicants with criminal histories in a manner consistent with the requirements of the LA City Fair Chance Initiative for Hiring Ordinance.
$70.3k-72k yearly 4d ago
Quality Engineer
Stevanato Group
Quality engineer job in Ontario, CA
Quality Engineer supports all aspects of the Quality Management System, Product Realization and Manufacturing Process Controls. Working with cross functional partners, defines and generates quality control plans, production process controls and procedures. Leads and supports validations including statistical analysis. Engages with customers to address quality issues and define acceptance criteria/attributes.
Essential Job Functions and Responsibilities:
Support the development and manufacturing of medical devices in conformance with applicable ISO 13485 requirements. Responsible for quality planning of all new development programs and design transfers to production.
Ensure policies and procedures comply with regulations and external standards, including software regulations, risk management, and change control.
Interact and form constructive working relationships with all levels of leadership within Quality, Procurement, Marketing, Engineering, and Operations.
Collaborate with Program Managers, Process Engineers, and/or Validation Engineers to execute process and equipment qualifications.
Problem Resolution: identification, data collection and trend analysis, reporting, and initiation of corrective and/or preventive action as well as reporting out of Key Metrics.
Identify opportunities and implement solutions to drive continuous improvement in performance metrics.
Investigate customer complaints, corrective actions and trending to drive improvements. * Plan and perform regular audits of quality system and drive system improvements through the Internal Audit and Quality Event Management (CAPA, NCR, Complaint etc.)
Monitoring and improvement of SPC systems, sampling plans and statistical methods. * Back-up and or perform to Head of Site Quality/Supervisor Representative, as assigned.
Plan, prepare, and execute Internal Audits, as assigned.
Participate in Material Review Board and/or Change Control Board as QA representative.
Utilize tools, gauges and other inspection equipment to obtain product specification data * Expert in utilizing hand measurement tools (Caliper, Micrometer, Ruler, Gage Blocks, height gage, etc.).
High Proficiency with PCDMIS inspection software utilizing CMM's: Brown, Sharpe, Hexagon, Smart scope.
Expert with utilizing ANSI Sampling Plans, IQMS, Minitab, Excel and Microsoft Word
High Proficiency in material analysis (i.e. FTIR, Melt Flow Testing, etc.)
Ability to read and decipher blueprints * Proficient in metrology and calibration.
Working knowledge of statistical methods for manufacturing.
Proficient in Geometric Dimensioning and Tolerancing (ANSI Y-14.5)
Requirements:
Minimum Education: five (5) years' experience in a similar field. Working knowledge in problem solving methodologies. Excellent oral and written communication skills.
Minimum Experience: At least two (2) year experience in a supervision and/or management role. Demonstrated experience to lead teams and projects. Good organizational skills. Previous experience in plastic injection molding related environment.
Demonstrated experience to lead teams and projects. Good organizational skills. Previous experience in plastic injection molding related environment.
Working in a medical device or other FDA regulated industry. Comprehensive understanding of ISO 9001, ISO 13485, JPAL MHLW Ordinance 169, and/or FDA QSR regulatory requirements. Computer literate with working knowledge of MS Word, Excel, and Access.
Desired candidate will have prior work history in MSA, SPC, Mini-tab, Infinity, sterilization, & clean room environment. *Knowledge, Skills, and Abilities
A working knowledge of FDA cGMP, ISO13485 requirements
A working knowledge of medical device manufacturing quality systems.
Working knowledge of Statistical Methods used in manufacturing. * PC-DMIS knowledge a plus.
Education and/or Experience:
3-7 Years in Quality Engineering in manufacturing and/or quality assurance.
Training in applicable ISO 9001, ISO 13485.
Experience using Minitab.
Proficient in metrology and calibration standards.
Proficient in Quality Audit concepts.
FDA quality standards experience a plus.
Certifications such as ASQ CQE, CQA, CQM
Warehouse areas (limited)
Will be required to perform other duties as requested, directed or assigned.
$77k-102k yearly est. 3d ago
Divisional Quality Manager, Materials Testing West
Element Materials Technology 4.4
Quality engineer job in Huntington Beach, CA
ID 2026-18148
Element has an opportunity for a Division Quality Manager for Material Testing West to join its team of quality professionals. This role is an essential member of the management team and responsible for the overall quality performance of multiple locations in our Aerospace business. This role is critical in ensuring product quality testing meets the highest aerospace standards, enabling regulatory compliance, customer satisfaction, and operational excellence.
As part of the business unit (BU) leadership team, you'll shape and deploy quality programs that support test reliability, consistency, and lab readiness and drives business growth, operational performance, customer satisfaction, and EBITDA improvement. You'll champion a strong quality culture, guiding local quality leaders, driving standardization, and engaging with aerospace primes, auditors, and accreditation bodies.
With strong leadership skills, your ability to influence and lead colleagues in a dynamic, cross-functional matrix environment is essential. You will work closely with the Division Director, location Quality Managers and location General Managers to ensure that Element quality policies, processes and procedures are effectively implemented. As a quality leader within Element you will be capable of driving a culture of quality assurance and quality improvement in the Division.
You will work with the other Division Quality Managers to share best practice and build a strong quality community, so effective interpersonal skills are a key requirement.
Compensation: $143,750 - $172,500/year Depending on Experience
Responsibilities
Ensure consistent execution of the Quality Management System (QMS) aligned with ISO/IEC 17025, AS9100, Nadcap and Nuclear standards.
Lead quality strategy across the BU with a strong focus on product testing performance and compliance.
Drive lab readiness for audits and certifications; liaise with OEMs, regulatory bodies, and customers.
Guide and develop site-level quality teams; promote a culture of accountability and continuous improvement.
Improve key metrics including First Time Right (FTR) and Cost of Poor Quality (COPQ) through data-driven quality initiatives.
Standardize testing processes across labs to reduce risk and enhance data integrity.
Establish and implement applicable measurements / metrics for monitoring system effectiveness and to enable managers/employees to make sound quality decisions.
Use data analytics and quality tools to identify improvement opportunities, coach employees in problem-solving, and lead teams in effective corrective actions.
Establish collection and analysis systems of statistical data, forecast trends, propose solutions and drive process improvements.
Collaborate with HR and operational leaders to inspire, develop, and retain quality talent across the business unit.
Skills / Qualifications
Bachelor's degree (or equivalent education/experience) in engineering, science, or related technical discipline.
7+ years of quality management experience in aerospace, energy, defense, or related complex technical environments.
Deep knowledge of quality systems and standards including ISO/IEC 17025, AS9100, and Nadcap.
Proven success in managing multi-site quality functions in a matrix structure.
Strong experience interfacing with aerospace primes, accreditation bodies, and regulatory agencies.
Skilled in audit management, root cause analysis, and performance metrics.
Excellent communication and stakeholder engagement skills.
Excellent interpersonal and communication skills, able to build trust and credibility with internal and external stakeholders.
Willing to travel approximately 20%, including overnight stays within the US.
Company Overview
Element is one of the fastest growing testing, inspection and certification businesses in the world. Globally we have more than 9,000 brilliant minds operating from 270 sites across 30 countries. Together we share an ambitious purpose to 'Make tomorrow safer than today'.
When failure in use is not an option, we help customers make certain that their products, materials, processes and services are safe, compliant and fit for purpose. From early R&D, through complex regulatory approvals and into production, our global laboratory network of scientists, engineers, and technologists support customers to achieve assurance over product quality, sustainable outcomes, and market access.
While we are proud of our global reach, working at Element feels like being part of a smaller company. We empower you to take charge of your career, and reward excellence and integrity with growth and development.
Industries across the world depend on our care, attention to detail and the absolute accuracy of our work. The role we have to play in creating a safer world is much bigger than our organization.
Diversity Statement
At Element, we always take pride in putting our people first. We are an equal opportunity employer that recognizes diversity and inclusion as fundamental to our Vision of becoming "the world's most trusted testing partner".
All suitably qualified candidates will receive consideration for employment on the basis of objective work related criteria and without regard for the following: age, disability, ethnic origin, gender, marital status, race, religion, responsibility of dependents, sexual orientation, or gender identity or other characteristics in accordance with the applicable governing laws or other characteristics in accordance with the applicable governing laws.
$143.8k-172.5k yearly 4d ago
Quantum Control Software Engineer: Build Next-Gen QC Apps
Q-CTRL
Quality engineer job in Los Angeles, CA
A leading quantum technology firm based in San Francisco is seeking a Software Engineer to develop software solutions for quantum technologies. You will integrate systems, implement innovative techniques, and mentor junior developers. The ideal candidate has a degree in a STEM field and at least 4 years of programming experience with Python, Rust, or C++. This competitive role offers substantial salary and benefits along with a high-performance culture focused on flexibility and equity potential.
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$69k-91k yearly est. 2d ago
Process Development Engineer
ACL Digital
Quality engineer job in Thousand Oaks, CA
Ideal Candidate: 2-4 years of relevant experience working in drug and animal cells. Strong process knowledge. Experience purifying cells (biologics purifications), drug substance GMP manufacturing.
Previous Client or biotech experience is a plus.
Seeking a Process Development Engineer to join the Drug Substance Technology Engineering team at our Thousand Oaks facility. Providing process engineering support for human therapeutic products in clinical development through commercial production, our mission is to translate developmental processes to commercial reality for patients through scientific expertise and engineering innovation.
The Engineer will apply purification process engineering knowledge in support of technology transfer and clinical/commercial drug substance manufacturing in an innovative manufacturing suite using single-use technology. Will partner with manufacturing, quality, analytical, and bench scientists to support a highly dynamic manufacturing facility.
* onsite a minimum of 3 days a week
**Must have biotech background/experience, plus must have purification experience
$83k-110k yearly est. 1d ago
Packaging Engineer
Counter 4.3
Quality engineer job in Los Angeles, CA
Company: Counter
Job Title: Packaging Engineer
Reports To: Director of Sourcing and Director of New Product Launches
About Us
We are a startup revolutionizing beauty with a purpose; create the industry standard of “clean”. Our premium skincare, makeup, and body care formulations combine uncompromising safety, efficacy and environmental responsibility. And our vision transcends products. We are committed to inspiring confident women and others to recognize their collective power to create meaningful change. Our innovative community-commerce ecosystem connects customers, beauty enthusiasts, and loyalists, allowing each person to align with our brand in ways that authentically reflect their values and aspirations. From our formulas to our advocacy efforts to our community connection, we lead clean.
The Role
The Packaging Engineer will be responsible for developing, sourcing, and executing high-quality, cost-effective packaging solutions that meet brand, quality, and sustainability standards. This role partners closely with cross-functional teams, including Product Development, Operations, and Sourcing, to support new product launches and ongoing production needs.
The Packaging Engineer will oversee component development, supplier management, and production readiness while driving process improvements to enhance efficiency and reduce costs.
Key Responsibilities
Packaging Development & Engineering
• Translate creative design concepts into functional, manufacturable, and cost-effective packaging solutions
• Collaborate with Design, Product Development, and Sourcing to ensure packaging aligns with brand standards, functionality, and cost objectives
• Interpret and approve engineering documents, including die lines, material specifications, and technical drawings
• Provide subject-matter expertise to ensure packaging feasibility and production readiness
• Lead design reviews and recommend improvements to enhance sustainability, quality, and efficiency
• Oversee tooling development, including status tracking, vendor coordination, and cost management
Supplier Management & Sourcing
• Lead supplier evaluations, RFQs, and cost of goods (COGs) analyses to ensure quality, value, and timely delivery
• Build and maintain strong relationships with packaging vendors and contract manufacturers
• Identify cost drivers and apply a total cost of ownership approach to decision-making
• Manage packaging component orders and monitor supplier performance for cost, quality, and delivery
• Conduct on-site visits for supplier assessments, color matching, and first production runs as needed
Production Planning & Quality Assurance
• Coordinate with suppliers and internal teams to ensure on-time delivery of packaging components for production and new product launches
• Oversee packaging inventory levels to support production planning and business continuity
• Support first production runs through on-site quality assurance and troubleshooting
• Collaborate cross-functionally with Supply Chain, Planning, and Logistics to ensure readiness for on-time launches
• Drive initiatives to reduce waste, streamline processes, and improve overall packaging sustainability
Process Improvement & Cross-Functional Collaboration
• Develop and implement best-in-class packaging development processes, documentation, and tools
• Partner with Product Development, Regulatory, Planning, Finance, and Logistics to ensure seamless cross-functional alignment
• Champion continuous improvement initiatives and contribute to operational excellence
• Support packaging technology transfers and process standardization across product lines
Qualifications Required
• Bachelor's degree in Packaging Science, Industrial Design, Engineering, or a related field
• 5-6+ years of experience in packaging development, preferably within the beauty, skincare, or consumer goods industry
• Strong knowledge of packaging materials, manufacturing processes, and structural engineering principles
• Proven experience conducting RFQs, COGs analyses, and managing supplier relationships
• Excellent communication, organization, and project management skills
• Advanced Excel proficiency and familiarity with ERP systems (e.g., NetSuite, SAP, Oracle)
• Ability to work independently and collaboratively in a fast-paced, high-growth environment
Preferred
• Experience with sustainability initiatives and waste-reduction strategies
• Knowledge of clean beauty standards and eco-conscious materials
• Familiarity with PLM systems and technical documentation best practices
• Willingness to travel for supplier meetings, production evaluations, and quality reviews
Counter is a people-powered movement that starts with those behind it! We're building a team that reflects the diversity of the communities we serve, where every individual is respected, supported, and empowered to thrive.
We know that different backgrounds, identities, and perspectives make us stronger, more creative, and better equipped to drive change. That's why we're committed to fostering an inclusive culture where everyone belongs.
Counter is proud to be an Equal Opportunity Employer. We do not discriminate based on race, color, religion, sex, sexual orientation, gender/gender identity or expression, age, national origin, disability, veteran status, or any other legally protected status. We encourage all individuals to apply and join us in shaping a cleaner, more inclusive future for all.
$54k-84k yearly est. 19h ago
Packaging Engineer
Prokatchers LLC
Quality engineer job in El Segundo, CA
• Packaging support & testing: prepare and set up test requests for new materials/components; evaluate test reports; coordinate Greenpoint data requests.
• Data & documentation: perform project data cleanup, maintain project files and LIMS/PLM inputs; ensure accurate documentation for transfers.
• Sustainability & L4TF initiatives: support team efforts on sustainable materials, recyclability checks and L4TF data collection.
• Project collaboration: follow up on action items, liaise with cross‑functional stakeholders (R&I, Supply Chain, Quality), and support implementation steps from concept to launch.
• Supporting on diverse project work, including data gathering and follow-ups.
• Assist in preparing and setting up test requests for new materials and components.
• Perform data cleanup and organization for project documentation.
• Coordinate requests for Greenpoint data and evaluate test reports to inform project decisions.
• Contribute to L4TF initiatives, supporting sustainability efforts.
• Gain real-time experience by actively participating in project development steps, from conception to implementation.
Required:
• Currently pursuing or recently completed degree in Packaging/Mechanical/Materials Engineering or equivalent.
• Entry-level (0-1 year) technical support experience or academic project work.
• Mandatory: Business-level English.
$89k-125k yearly est. 1d ago
Packaging Engineer
Strategic Employment Partners (Sep 4.5
Quality engineer job in Industry, CA
Our client, a private label manufacturer in the CPG foods space, is seeking a Packaging Engineer to join their growing team. This role will involve leading packaging design and development, supporting sourcing and procurement efforts, and managing packaging testing protocols.
Term: Full Time/Permanent
Location: City of Industry (onsite)
Compensation: $90k - $120k/year
Desired Qualifications:
3+ years of experience in a packaging engineering-focused role
Experience designing flexible and rigid packaging elements
Experience with testing protocols (ISTA, ASTM, similar)
Experience in the food/beverage industry is a big plus
Degree in Packaging Engineering, or similar
$90k-120k yearly 4d ago
Process Engineer Level 2
Bykowski Equipment and Engineering Co
Quality engineer job in Chino, CA
About Bykowski Equipment Co.
Founded in 1967, Bykowski Equipment specializes in engineering solutions, custom fabrication, installations, parts, and services for the food manufacturing industry. We focus on custom sanitary systems for the Food, Beverage, Cosmetics, and Pharmaceuticals sectors. Joining our team means playing a role in our sustained organic growth.
Job Overview
We are seeking a Process Engineer knowledgeable in the design and construction of sanitary process piping systems, preferably in the food and beverage manufacturing industry. This role requires a working knowledge of process flow diagrams, P&IDs, BTU heat calculations, pressure drop calculations, piping design, and automation controls integration. Applicants should be able to engineer process piping systems with minimal oversight from management.
Key Responsibilities
1. Design and Troubleshoot Process Solutions: Develop innovative solutions and troubleshoot issues within manufacturing processes.
2. Create and Interpret Process Flow Diagrams and P&IDs: Produce detailed PFDs and P&IDs essential for accurate project execution.
3. Design Layouts for Plant Systems: Plan and design comprehensive layouts for plant systems, ensuring efficient space utilization and system integration.
4. Perform Essential Process Calculations: Carry out critical calculations for BTU, heat transfer, and pump sizing, contributing to accurate project cost estimations.
5. Coordinate Site Visits with Clients: Organize and conduct site visits to document and verify current processes, layouts, and to create accurate PFDs.
6. Develop Process Requirements with Clients: Work closely with clients to outline specific process requirements, including flow rates and product viscosity.
7. Keep Clients Updated: Maintain regular communication with clients regarding project progress, lead times, and expected delivery dates.
8. Manage Job Schedules: Efficiently schedule projects to minimize downtime and ensure timely completion.
9. Engineer Conceptual Process Solutions: Conceptualize and design process solutions, expanding from our library of existing designed systems.
10. Troubleshoot Manufacturing Process Issues: Identify and solve problems within the designed processes, ensuring optimal operation.
11. Create Detailed Process Descriptions and Operation Sequences: Document processes and operational steps to provide clear instructions for project execution.
12. Design and Develop Comprehensive 2D P&ID Flow Diagrams and 3D Models: Utilize design skills to create detailed diagrams and models for project planning and implementation.
13. Produce Drawing Packets and Design Parts for CNC Operations: Prepare necessary documentation and designs for manufacturing and assembly.
14. Provide Instructions to Shop Fabricators: Offer guidance and support to fabricators under the supervision of the engineering manager ensuring that fabrications align with construction drawings and project standards.
15. Engage with Vendors for Cost-effective Solutions: Collaborate with vendors to obtain the best pricing and solutions for project components.
16. Estimate Labor Costs and Manage Project Timelines: Oversee budgeting and scheduling to ensure projects are completed within scope and on time.
17. Utilize ERP System for Equipment Pricing: Use our ERP system to determine the pricing of parts depicted in drawings, aiding in the pricing of systems for sales proposals to customers.
QualificationsRequired
• Bachelor of Science Degree in Mechanical Engineering, Chemical Engineering, or an equivalent of 4 years of related processing industry experience.
• Experience in mechanical drafting using AutoCAD, Plant 3D, and Inventor (or equivalent).
• Must have experience in Microsoft Office programs.
• Knowledge of creating a P&ID Process Flow Diagram.
• Knowledge of process design or piping design for liquid-based sanitary processing systems.
• Knowledge of Fluid Dynamics and fluid pressure drop calculations for process piping.
• Knowledge of Thermodynamics and heat transfer.
Preferred
• Knowledge of centrifugal, positive displacement pumps, and heat exchanger sizing. (BEECO will train candidates.)
• Exposure to welding/fabrication practices.
• Familiarity with CNC laser and mechanical press brake equipment.
• A strong mechanical aptitude; sharing personal DIY projects is encouraged.
Benefits
• 401(k), Dental, Vision, and Life Insurance.
• Health Insurance (HMO & PPO options), Flexible Spending Accounts.
• Paid Time Off, Sick Time, and Paid Holidays.
• Professional growth and training opportunities.
How to Apply
Interested candidates should visit Indeed.com and search for "Process Engineer II at Bykowski Equipment Co." in the Southern California Region to find our listing. Follow the instructions to apply directly or save the job for later application. We look forward to your application and potentially welcoming you to our team.
$108k-144k yearly est. 2d ago
Manufacturing Test Engineer
Motion Recruitment Partners LLC 4.5
Quality engineer job in Costa Mesa, CA
Job Title: Manufacturing Test Engineer (Electrical)
Engagement Type: 1-Year Contract (with possible extension)
Pay Rate: $26-$32.00/hour
Schedule: Monday-Friday | 100% Onsite | 6:00 AM-2:00 PM (PST)
Position Overview
We are seeking a Test Equipment Technician to support manufacturing and test engineering operations at our Costa Mesa facility. This is an immediate need role focused on the maintenance, troubleshooting, and repair of test fixtures and equipment in accordance with Schneider Electric test engineering and quality standards. The ideal candidate will have a strong electrical engineering background, hands-on test experience, and exposure to high-voltage systems.
Key Responsibilities
Perform detailed maintenance, troubleshooting, and repair of test fixtures and test equipment
Ensure all test equipment is properly maintained, calibrated, and operational
Collaborate closely with Test Engineers to diagnose issues and resolve equipment failures
Execute preventive and corrective maintenance tasks to maximize equipment availability, efficiency, and effectiveness
Support workflow scheduling and complete required administrative documentation
Ensure assigned tasks are completed accurately and within established timelines
Adhere to all quality, safety, and engineering procedures
Perform other related duties as assigned
Required Qualifications
Associate degree (AA/AS) in Electrical Engineering or Electrical Technology and 4+ years of related experience
OR
Certificate from a recognized technical trade school (or advanced military technical training) plus 4+ years of related experience
OR
High School Diploma or GED (required) with equivalent hands-on technical experience
Strong hands-on experience with test equipment and electrical systems
Ability to use electronic test and measurement equipment, including DVMs and oscilloscopes, and accurately interpret results
Proficiency with basic hand tools and soldering techniques
Strong written and verbal communication skills in English
Basic computer proficiency, including Microsoft Word and Excel
Good color vision for identifying color-coded wiring and cabling
Preferred Qualifications
Experience working with high-voltage systems (up to 480V)
Manufacturing or test environment experience
Electrical Engineering (EE) background
Top Skills
Test Equipment Maintenance & Troubleshooting
Electrical Engineering Fundamentals
High-Voltage Testing (480V preferred)
Test Fixtures & Manufacturing Test Systems
$26-32 hourly 4d ago
Plan Check Engineer
City of Corona, Ca 3.4
Quality engineer job in Corona, CA
The City of Corona is seeking a detail-driven and solutions-oriented Plan Check Engineer to play a vital role in shaping safe, sustainable, and thriving spaces for generations to come. In this dynamic role, you'll be at the forefront of community development-reviewing complex architectural and structural plans, interpreting building codes, and collaborating with top-tier professionals to ensure every project is up to standard.
Knowledge
Theories and principles of structural design, engineering mathematics and soils engineering.
Approved building construction methods, materials and proper inspection methods related to residential, commercial and industrial developments.
Federal, state and municipal codes and regulations governing housing and building construction, rehabilitation, alteration, use and occupancy, including the Model or California Building, Plumbing, Mechanical, Energy, Fire and Electrical Codes.
Appropriate safety and fire prevention construction and building methods.
Education and Experience:
Education:
Graduation from a four-year college or university with major course work in architecture or civil, structural, or architectural engineering.
Experience:
Three (3) years of increasingly responsible professional plan checking experience; or an equivalent combination of training and experience.
Special Requirements
A valid Class C California driver's license and the ability to maintain insurability under the City's Vehicle Insurance Policy.
Registration as a Professional Engineer with the State of California Department of Consumer Affairs - Board for Professional Engineers, Land Surveyors, and Geologists. Certification as a Building Plans Examiner by ICC is required, or ability to obtain within one year of employment date.
Skills & Abilities
Plan, organize, perform detailed analysis and examination of building and construction designs, specifications and plans.
Apply engineering and architectural principles and techniques to solve complex residential, commercial and industrial construction problems and objectives.
Analyze structural integrity and load factors using engineering design mechanics.
Analyze and evaluate complex building plans, data and reports to determine whether compliance has been achieved.
Prepares correspondence to architects, engineers and contractors relating to the correction of plans and engineering detail; initiates notifications of code violations.
Advises Building Inspectors on structural and other building-related problems arising in the field during construction.
Prepares and conducts training programs for plan check, inspection, and counter personnel.
Licenses and Certifications:
A valid Class C California driver's license and the ability to maintain insurability under the City's Vehicle Insurance Policy.
Registration as a Professional Engineer with the State of California Department of Consumer Affairs - Board for Professional Engineers, Land Surveyors, and Geologists with a status of good standing and not suspended or revoked.
Certification as a Building Plans Examiner by ICC is required, or ability to obtain within one year of employment date.
Application Process
Applications will be accepted on a continuous basis until a sufficient number of qualified applications have been received. The deadline for first review of applications is Tuesday, August 19, 2025. The selection process will consist of a review and evaluation of all applicants' qualifications. Those applicants deemed to possess the most desirable qualifications will be invited to participate in a possible virtual HireVue and oral interview. The top scoring candidates from the oral interview will be placed on an eligibility list from which the department may hire. The eligibility list established from this recruitment may also be used to fill the current and/or additional vacancies throughout the City.
COMMUNITY
A City whose heritage spans more than 125 years, the City of Corona, located in Riverside County, California, encompasses approximately 40 square miles and has a vibrant, culturally diverse population of approximately 170,000 residents. Residents of Corona enjoy a variety of cultural, recreational, and educational opportunities that provide a first-rate quality of life for its residents and visitors. Within an hour's travel time, outdoor enthusiasts can enjoy winter activities such as snowboarding and skiing and summer activities including surfing, boating, or simply relaxing on world class beaches. Corona's economy is strong and getting stronger; more than 84,000 people work here. Our retail, commercial, and housing areas are expanding, and office development continues to be strong.
THE ORGANIZATION
The City of Corona is a General Law city operating under a Council-Manager form of government. Policy making and legislative authority is vested in the City Council, consisting of a Mayor and four Council Members. Members of the City Council are elected by District to a four-year term. The Mayor is selected by the Council and serves as the presiding officer for one year.
The City is organized into the following departments/organizational units: Community Services, City Manager's Office, Economic Development, Finance, Fire, Human Resources, Information Technology, Legal and Risk Management, Police, Planning & Development, Public Works, and Utilities. Oversight of these departments is divided between the City Manager and an Assistant City Manager.
The City's total operating budget for Fiscal Year 2026 is $422.7 million with a General Fund operating budget of $231.3 million. Corona enjoys a workforce of 935 dedicated employees who provide high-quality services to its residents and visitors each day.
ESSENTIAL DUTIES AND RESPONSIBILITIES
To view the essential duties and responsibilities, click here.
QUALIFICATIONS GUIDELINES
To view the qualifications guidelines, click here.
PHYSICAL/MENTAL DEMANDS AND WORK ENVIRONMENT
To view the physical/mental demands and work environment, click here.
$81k-100k yearly est. 4d ago
Program Manager Quality Improvement
Apidel Technologies 4.1
Quality engineer job in Newport Beach, CA
Job Description
Responsible for establishing and continuing eective quality improvement eorts to achieve organizational performance goals and national top decile performance in clinical excellence. Quality improvements may be small or large scale and are in alignment with Hoags strategic goals for example, addressing 30-day readmissions and mortality reduction. The Quality Improvement Manager may apply Lean, Six Sigma, and other quality improvement methodologies to deliver results.
Job Responsibilities:
Coaches and trains teams in the utilization of improvement tools and implementation of improvements.
Manages plans and develops guidelines, process measures, targets, and standards for monitoring and measuring results to deliver on goals.
Interacts daily with leaders, to identify, dene, and manage opportunities to improve quality while helping create a strategic approach to produce and establish extraordinary improvement.
The Program Manager Quality Improvement collaborates to lead and organize eorts for continuous clinical improvement.
Skills:
Required Skills & Experience:
Advanced training or experience in performing statistical, financial and strategic analysis
Five years experience in performance/process improvement projects including but not limited to Lean, Six Sigma methodologies
Demonstrated performance improvement and process improvement skills and knowledge of methodologies such as Lean, Six Sigma, DMAIC, and PDCA
Highly proficient in Microsoft Project and the Microsoft Office Suite (Word, Excel, PowerPoint, Visio)
Comprehensive digital marketing skills
Preferred Skills & Experience:
Experience managing healthcare-related projects and familiarity with healthcare provider industry
Seven years experience in performance/process improvement projects preferred.
Education:
Required Education:
Bachelors degree in Industrial Engineering, Business/Healthcare Administration, Life Sciences or equivalent Medical Foundation, Physician Practice or Health Plan related experience
Preferred Education:
Masters degree in Industrial Engineering, Business/Healthcare Administration, or Public Health
Consulting experience
OR
Masters degree in Healthcare Administration or Public Health.
Required Certifications & Licensure:
N/A
Preferred Certifications & Licensure:
Certifications in Lean and/or Six Sigma Methodology
Project Management Professional (PMP) certification
This is the pay range that RightSourcing (a part of Magnit) reasonably expects to pay someone for this position, however, as a supplier your expected pay range may vary and/or include certain benefits like: Stipends (for clinical traveler workers only), Medical, Dental, Vision, 401K [include any compulsory benefits such as commissions, incentive bonuses, etc. if applicable].
Schedule Notes:
2 Openings for Quality Management Team - Roles are very specific - candidates must have in-depth experience in Clinical Quality Improvement in a hospital inpatient setting. Contract to Hire opportunities for the right talent. 100% Onsite *Candidates must possess all 4 of the below or they will not be considered: 1. Completed PI training and certification (six sigma, lean, CPHQ, Masters in Improvement) from nationally recognized organizations (e.g., ASQ). 2. Current or past formal position in Quality Improvement/Performance improvement (minimum 2 years) 3. History of leading and improving quality outcome metrics such as readmissions, mortality, hospital acquired conditions (infections, falls, pressure injuries, medication errors), sepsis care, venous thromboembolism, unplanned extubations, delirium, complications, c-section, exclusive breastfeeding, etc). 4. Experience using key driver diagrams, pareto charts, excel pivot tables, project management tools
$87k-132k yearly est. 10d ago
Supplier Quality Program Manager
Northwoodspace
Quality engineer job in Los Angeles, CA
About Northwood:
Northwood is on a mission to transform connectivity between earth and space and bring the benefits of space to the masses through innovations in space communications technologies. If you like building quickly and seeing your work deployed in locations around the globe with real impact, we want you at Northwood.
Role:
We're looking for a Supplier Quality Program Manager to be Northwood's first quality-focused hire - a builder, systems thinker, and technical leader who will define how we scale manufacturing excellence across our global supply chain.
You will create Northwood's supplier quality program from the ground up, partnering closely with engineering and operations to ensure our products are designed and built for long-term reliability. From designing scalable systems to defining rigorous standards, you'll establish the foundation for a world-class supplier quality organization and cultivate a company-wide culture of quality and accountability.
As Northwood grows, you'll have the opportunity to build and lead a high-performing team, mentoring future engineers and shaping how high-reliability hardware moves from concept to production. You'll influence how quality scales across our global supply base and how it becomes woven into every stage of development and delivery.
This is a foundational, high-impact role - perfect for someone who loves creating structure from ambiguity, leading through influence, and leaving a lasting mark on both our culture and the future of space communications.
Responsibilities:
Design and launch Northwood's first supplier quality management system, from process design to documentation and continuous improvement
Shape the supply base: Identify, qualify, and develop world-class suppliers for RF, PCBA, mechanical, and electromechanical components
Lead audits, performance reviews, and corrective actions that elevate quality and delivery across our network
Partner closely with design, manufacturing, and operations on DFM, NPI, and pilot builds - ensuring every part is production-ready
Define supplier KPIs (quality, cost, responsiveness) and implement real-time visibility tools that drive accountability and progress
Act as the technical and quality liaison between internal engineering and external suppliers - turning insights into scalable, repeatable success
Drive supplier readiness for production ramp-ups and capacity expansions as Northwood grows around the world
Lead root cause analysis and corrective/preventive actions (NCR/CAPA) to eliminate defects and strengthen design for manufacturability
Partner with suppliers on process improvements that cut costs, reduce cycle times, and maximize yields
Establish quality requirements and flow downs that ensure every product built by our partners reflects Northwood's commitment to excellence
Basic Qualifications:
Bachelor's degree in Mechanical, Electrical, Industrial Engineering, or related field
7+ years in Supplier Quality, Supplier Development, or Manufacturing Quality roles
Experience with quality standards and tools (e.g., ISO 9001, AS9100, PPAP)
A track record of building or scaling quality systems in low-to-medium volume, high-complexity environments
Proven success qualifying and managing suppliers and driving measurable performance improvement
Willingness to travel up to 25% domestically and internationally to engage with our global supply network
Preferred Qualifications:
Background in aerospace, satellite, telecommunications, or defense industries
Hands-on experience with RF, PCBA, custom enclosures, or electromechanical assemblies
Familiarity with ERP, PLM, or digital quality management systems
Experience supporting early-stage product development through production ramp
Lean Six Sigma or similar certifications
Strong data fluency - proficiency with SQL or analytics tools for supplier and quality insights
$119k-172k yearly est. Auto-Apply 16d ago
Quality Patient Safety Program Manager Licensed
Common Spirit
Quality engineer job in Oxnard, CA
Job Summary and Responsibilities The Quality Patient Safety Program Manager is a key leader responsible for supporting and implementing the organization's comprehensive quality and patient safety programs. This role collaborates closely with various departments, clinical teams, and stakeholders to proactively identify opportunities for improvement, rigorously analyze data, and implement evidence-based practices to enhance patient outcomes, minimize risks, and foster a culture of safety. The ideal candidate will be a Registered Nurse with a strong clinical background, a demonstrated passion for quality improvement, exceptional analytical and communication skills, and proven leadership experience.
* Support the implementation and maintenance of the organization's quality and patient safety programs, ensuring alignment with regulatory requirements, accreditation standards, and best practices.
* Collect, analyze, and interpret data related to patient safety, quality metrics, and clinical outcomes.
* Participate in the investigation and analysis of adverse events, near misses, and sentinel events.
* Develop and implement evidence-based protocols and guidelines to improve clinical practice.
* Develop and deliver training programs on quality improvement, patient safety, and risk management to clinical and non-clinical staff.
* Communicate effectively with all levels of the organization, including senior leadership, regarding quality and patient safety issues.
* Ensure compliance with all applicable regulatory requirements, accreditation standards, and organizational policies.
* Provide coaching, mentoring, and performance feedback to team members.
Job Requirements
Minimum Qualifications
* Bachelors degree
* Minimum of five (5) years of risk management, patient safety, quality compliance, and/or other related professional experience, and a minimum of five (5) years of experience managing/supervising employees and/or vendors.
* CA RN Licence
Skills & Abilities:
* Strong clinical background and understanding of healthcare operations.
* Demonstrated knowledge of quality improvement methodologies (e.g., Lean, Six Sigma, PDSA).
* Excellent analytical and problem-solving skills.
* Proficiency in data analysis and reporting.
* Strong communication, interpersonal, and presentation skills.
* Ability to work effectively in a team environment.
* Knowledge of regulatory requirements and accreditation standards (e.g., The Joint Commission, CMS).
* Proficient in Microsoft Office Suite (Word, Excel, PowerPoint).
Where You'll Work
St. John's Regional Medical Center, located in Oxnard, California is a recognized as a Top 250 Hospital in the Nation and as one of America's 100 Best Hospitals for Cardiac Care by Healthgrades. St. John's Regional is a part of Dignity Health's Southern California Division and is a member of CommonSpirit Health, the largest not-for-profit health care system in the nation, boasting an integrated network of top quality hospitals, with physicians from the most prestigious medical schools, and comprehensive outpatient services - all recognized for quality, safety, and service. Each hospital is supported by an active philanthropic Foundation to help meet the growing health care needs of our communities. Learn more here at **************************************
One Community. One Mission. One California
$121k-174k yearly est. 2d ago
Quality Patient Safety Program Manager Licensed
Commonspirit Health
Quality engineer job in Oxnard, CA
Where You'll Work
St. John's Regional Medical Center, located in Oxnard, California is a recognized as a Top 250 Hospital in the Nation and as one of America's 100 Best Hospitals for Cardiac Care by Healthgrades. St. John's Regional is a part of Dignity Health's Southern California Division and is a member of CommonSpirit Health, the largest not-for-profit health care system in the nation, boasting an integrated network of top quality hospitals, with physicians from the most prestigious medical schools, and comprehensive outpatient services - all recognized for quality, safety, and service. Each hospital is supported by an active philanthropic Foundation to help meet the growing health care needs of our communities. Learn more here at **************************************
One Community. One Mission. One California
Job Summary and Responsibilities
The Quality Patient Safety Program Manager is a key leader responsible for supporting and implementing the organization's comprehensive quality and patient safety programs. This role collaborates closely with various departments, clinical teams, and stakeholders to proactively identify opportunities for improvement, rigorously analyze data, and implement evidence-based practices to enhance patient outcomes, minimize risks, and foster a culture of safety. The ideal candidate will be a Registered Nurse with a strong clinical background, a demonstrated passion for quality improvement, exceptional analytical and communication skills, and proven leadership experience.
Support the implementation and maintenance of the organization's quality and patient safety programs, ensuring alignment with regulatory requirements, accreditation standards, and best practices.
Collect, analyze, and interpret data related to patient safety, quality metrics, and clinical outcomes.
Participate in the investigation and analysis of adverse events, near misses, and sentinel events.
Develop and implement evidence-based protocols and guidelines to improve clinical practice.
Develop and deliver training programs on quality improvement, patient safety, and risk management to clinical and non-clinical staff.
Communicate effectively with all levels of the organization, including senior leadership, regarding quality and patient safety issues.
Ensure compliance with all applicable regulatory requirements, accreditation standards, and organizational policies.
Provide coaching, mentoring, and performance feedback to team members.
Job Requirements
Minimum Qualifications
Bachelors degree
Minimum of five (5) years of risk management, patient safety, quality compliance, and/or other related professional experience, and a minimum of five (5) years of experience managing/supervising employees and/or vendors.
CA RN Licence
Skills & Abilities:
Strong clinical background and understanding of healthcare operations.
Demonstrated knowledge of quality improvement methodologies (e.g., Lean, Six Sigma, PDSA).
Excellent analytical and problem-solving skills.
Proficiency in data analysis and reporting.
Strong communication, interpersonal, and presentation skills.
Ability to work effectively in a team environment.
Knowledge of regulatory requirements and accreditation standards (e.g., The Joint Commission, CMS).
Proficient in Microsoft Office Suite (Word, Excel, PowerPoint).
$121k-174k yearly est. Auto-Apply 2d ago
Program Manager Quality Improvement
Huckeye Health Services LLC
Quality engineer job in Newport Beach, CA
Job Description
Job Title: Program Manager Quality Improvement
Job Type: Contract to Hire
Department: Quality Management
Schedule: Full Time
Hourly Rate: $90- $100/hr depending on experience
Required Experience:
- Candidates must have in-depth experience in Clinical Quality Improvement in a hospital inpatient setting. *Candidates must possess all 4 of the below or they will not be considered: 1. Completed PI training and certification (six sigma, lean, CPHQ, Masters in Improvement) from nationally recognized organizations (e.g., ASQ). 2. Current or past formal position in Quality Improvement/Performance improvement (minimum 2 years) 3. History of leading and improving quality outcome metrics such as readmissions, mortality, hospital acquired conditions (infections, falls, pressure injuries, medication errors), sepsis care, venous thromboembolism, unplanned extubations, delirium, complications, c-section, exclusive breastfeeding, etc). 4. Experience using key driver diagrams, pareto charts, excel pivot tables, project management tools.
Required Education:
- Bachelor's degree in Industrial Engineering, Business/Healthcare Administration, Life Sciences or equivalent Medical Foundation, Physician Practice or Health Plan related experience
Preferred Skills & Experience:
-Master's degree in Industrial Engineering, Business/Healthcare Administration, or Public Health
-Consulting experience
Please apply online and email resume to: *************************************
$90-100 hourly Easy Apply 9d ago
Manufacturing Quality Manager
Professional. Career Match Solutions
Quality engineer job in Irvine, CA
Not remote Must be a USA Citizen Salary $79K to $118K plus bonus and benefits Six Sigma Certification QA Manager has managerial oversight of the Irvine site Quality Assurance organization and the Quality Assurance Department within it. The Quality Assurance responsibilities for a manufacturing plant in the aerospace and defense industry include developing, implementing, maintaining a robust quality system and measuring its effectiveness to assure that the products and processes meet internal quality standards and requirements established by customers and regulatory agencies. Our four pillars are Customer Centricity, Operational Excellence, Innovation, and People.
Responsibilities:
Manage a highly focused site quality organization, aligned with overall global quality expectations.
Directly Manage Quality Engineers, Inspection Supervisor and inspectors. Coordinating their activities and schedules to support the Site Production and Customer needs.
Ensures the products & services provided to customers meet customer requirements and regulatory standards at both the production & product evaluation level.
Ensures the compliance to Quality objectives (quality costs, product defects, customers satisfaction, etc) the effectiveness of corrective measures, and compliance to AS9100 as well as MIL-STD- 790.
Coordinates the fulfillment of the Inspection Procedures (Raw Material and/or Processes & Final Product) to ensure the Quality Requirements are achieved and maintained.
Develops and analyzes Process Performance through metrics of First Pass Yield, First Piece Inspection as well as using APQP methods.
Supports the management of business quality systems and applicable certification systems (ISO, MIL, AS, etc) including the development, maintenance & updating of documentation, processes, and records.
Represent the company before regulatory agencies (DLA, NavAir), Customers, and/or Certification Registrars.
Manages and participates in failure analysis, complaints, resolution & information request from customers.
Supports Continuous Improvement Programs, Lean Manufacturing, Six Sigma, etc.
Manage customer escapes, Notices of escapement and develop reports to track progress of investigations as well as corrective measures, while ensuring accuracy and timeliness of reporting to internal and external customers.
Manage day-to-day activities of the applicable organization including: goal setting, QE activity, Inspection activity and timeliness of those activities.
Develop, groom, train and manage talent by providing coaching and mentoring to build strong performing teams
Works effectively in a highly cross-functional environment, balancing multiple goals and priorities.
US Citizen
BS degree in a technical field
Strong managerial, communication and reporting skills
Overall technical experience in manufacturing processes and materials used in the connector industry.
3-5 years of direct experience in a Manufacturing/Quality
5 years of management experience leading highly focused technical organizations
Direct experience with APQP practices
Small assembly manufacturing
Proficient in Microsoft Word, Excel and PowerPoint. Experience in MS Project a plus
Lean Six Sigma certification
Familiarity with military, industry and aerospace standards such as Mil-STD-790, AS9100, ISO9001 and ISO17025
Experience with DLA or other Qualifying Activities as it relates to Mil qualified products
Span of Control: 8 - 12 engineers and technicians
How much does a quality engineer earn in View Park-Windsor Hills, CA?
The average quality engineer in View Park-Windsor Hills, CA earns between $68,000 and $117,000 annually. This compares to the national average quality engineer range of $61,000 to $103,000.
Average quality engineer salary in View Park-Windsor Hills, CA
$89,000
What are the biggest employers of Quality Engineers in View Park-Windsor Hills, CA?
The biggest employers of Quality Engineers in View Park-Windsor Hills, CA are: