59 Quality Assurance jobs in La Habra
Quality Assurance Nurse
Posted today
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Job Description
POSITION SUMMARY:
The Clinical Quality Assurance Nurse reviews cases and ensures all necessary information has been provided and is accurate before sending back to requestor. The Clinical Quality Assurance Nurse will also oversee the facility’s policies and procedures.
RESPONSIBILITIES/ACCOUNTABILITIES:
· Performs quality assurance review of peer review reports, correspondences, addendums or supplemental reviews.
· Ensures clear, concise, evidence-based rationales have been provided in support of all recommendations and/or determinations.
· Ensures that all client instructions and specifications have been followed and that all questions have been addressed.
· Ensures each review is supported by clinical citations and references when applicable and verifies that all references cited are current and obtained from reputable medical journals and/or publications.
· Ensures the content, format, and professional appearance of the reports are of the highest quality and in compliance with company standards.
· Ensure that the appropriate board specialty has reviewed the case in compliance with client specifications and/or state mandates and is documented accurately on the case report.
· Verifies that the peer reviewer has attested to only the fact(s) and that no evidence of reviewer conflict of interest exists.
· Ensures the provider credentials and signature are adhered to the final report.
· Identifies any inconsistencies within the report and contacts the Peer Reviewer to obtain clarification, modification or correction as needed.
· Assists in resolution of customer complaints and quality assurance issues as needed.
· Ensures all federal ERISA and/or state mandates are adhered to at all times.
· Provides insight and direction to management on consultant quality, availability and compliance with all company policies and procedures and client specifications.
· Promote effective and efficient utilization of company resources.
· Participate in various educational and or training activities as required.
· Perform other duties as assigned.
QUALIFICATIONS/SKILLS:
· LVN License required.
· Must be able to operate a general computer, fax, copier, scanner, and telephone.
Quality Assurance Engineer
Posted today
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Job Description
Project Description:
Become part of the latest generation of HMI development. In the environment of the most attractive automobile manufacturer in Germany. Benchmark technologies in the area of AR/HUD will be defined here.
Our team of experts accompanies development processes and goes into a validation focus that takes place very close to the vehicle. A real childhood dream for every engineer. Interest aroused?
Responsibilities:
- Design, develop, and execute test plans and test cases for IVI systems and connected services.
- Perform functional, regression, integration, and system testing across multiple hardware and software configurations.
- Automate test cases using industry-standard tools and frameworks.
- Analyze test results, identify defects, and work with development teams to resolve issues.
- Collaborate with cross-functional teams to define quality metrics and ensure compliance with automotive standards (e.g., ASPICE, ISO 26262).
- Participate in continuous improvement initiatives for QA processes and tools.
Mandatory Skills Description:
- Bachelor's or Master's degree in Computer Science, Electrical Engineering, or related field.
- 3+ years of experience in software QA, preferably in automotive or embedded systems.
- Strong understanding of IVI systems, CAN, Ethernet, and automotive communication protocols.
- Experience with test automation tools (e.g., Python, Robot Framework, Jenkins).
- Familiarity with version control systems (e.g., Git) and CI/CD pipelines.
- Knowledge of automotive standards and testing methodologies (e.g., ASPICE, ISO 26262).
- Excellent problem-solving skills and attention to detail.
- Fluent in English (spoken and written).
Quality Assurance Engineer
Posted today
Job Viewed
Job Description
Project Description:
Become part of the latest generation of HMI development. In the environment of the most attractive automobile manufacturer in Germany. Benchmark technologies in the area of AR/HUD will be defined here.
Our team of experts accompanies development processes and goes into a validation focus that takes place very close to the vehicle. A real childhood dream for every engineer. Interest aroused?
Responsibilities:
-Design, develop, and execute test plans and test cases for IVI systems and connected services.
-Perform functional, regression, integration, and system testing across multiple hardware and software configurations.
-Automate test cases using industry-standard tools and frameworks.
-Analyze test results, identify defects, and work with development teams to resolve issues.
-Collaborate with cross-functional teams to define quality metrics and ensure compliance with automotive standards (e.g., ASPICE, ISO 26262).
-Participate in continuous improvement initiatives for QA processes and tools.
Mandatory Skills Description:
Bachelor's or Master's degree in Computer Science, Electrical Engineering, or related field.
3+ years of experience in software QA, preferably in automotive or embedded systems.
Strong understanding of IVI systems, CAN, Ethernet, and automotive communication protocols.
Experience with test automation tools (e.g., Python, Robot Framework, Jenkins).
Familiarity with version control systems (e.g., Git) and CI/CD pipelines.
Knowledge of automotive standards and testing methodologies (e.g., ASPICE, ISO 26262).
Excellent problem-solving skills and attention to detail.
Fluent in English (spoken and written).
Nice-to-Have Skills Description:
-Experience with Android Automotive OS or QNX.
-Familiarity with HMI testing and UX validation.
-Exposure to cloud-connected vehicle services and OTA updates.
-Knowledge of cybersecurity testing in automotive environments.
-ISTQB certification or similar QA credentials.
-German language proficiency.
Quality Assurance Manager
Posted 2 days ago
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Job Description
Job Description
The Quality Assurance Manager leads and manages the quality function across our global supply chain, overseeing product quality from manufacturing at partner facilities to final assembly, testing, and control in California operations. The ideal candidate will bring hands-on experience in consumer electronics or LED lighting products and possess strong skills in quality systems, root cause analysis, and cross-functional leadership.
Responsibilities
+ Manage and mentor QA teams across multiple geographic locations.
+ Build and maintain a high-performance QA culture with accountability and continuous improvement.
+ Collaborate with HR and leadership to hire, train, and retain top QA talent in various regions.
+ Develop, implement, manage, maintain, and improve the Quality Management System (QMS) in compliance with ISO 9001, UL, CE, RoHS, etc.
+ Create and maintain Control Plans, SOPs, and test procedures for assembly and testing operations.
+ Establish quality KPIs and drive continuous improvement initiatives.
+ Lead internal audits, document control, and root cause investigations.
+ Ensure proper documentation of inspection results, nonconformance reports, audit reports, corrective actions, and quality records.
+ Prepare for and support third-party audits and certification renewals.
+ Work closely with contract manufacturers and suppliers to ensure product specifications, BOMs, and manufacturing processes are strictly followed.
+ Conduct quality audits, remote or on-site, and manage supplier performance scorecards.
+ Review and approve supplier quality plans, first article inspections, and ongoing production audits.
+ Coordinate and manage incoming quality checks for parts and subassemblies.
+ Support supplier corrective actions and continuous improvement initiatives.
+ Implement and supervise in-house quality inspection processes during assembly, testing, and packaging.
+ Develop and implement control plans, work instructions, and quality checkpoints for in-house assembly, testing, and verification of electrical, optical, and mechanical specifications.
+ Collaborate with engineering and production teams to ensure quality objectives are met on the production floor.
+ Monitor test data and product performance to identify trends, reduce defects, and improve processes.
+ Manage calibration and maintenance of testing equipment.
+ Collaborate with engineering, operations, and customer service teams to resolve quality issues and improve product reliability.
+ Lead root cause investigations and implement corrective/preventive actions (CAPA) for non-conformities, returns, or warranty claims.
+ Support failure analysis and improve product reliability through data-driven improvements.
+ Facilitate cross-functional quality reviews and continuous improvement meetings.
+ Support customer audits, product certifications, and compliance testing.
+ Train employees on quality processes and inspection procedures.
+ Manage post-shipment quality performance including customer returns, field failures, and warranty claims.
+ Collaborate with Customer Service and Sales to resolve issues and close the feedback loop to suppliers or internal processes.
+ Participate in cross-functional design reviews and NPI projects to ensure quality is built into products from the outset.
+ Serve as the quality point of contact from vendor onboarding through customer delivery, ensuring consistency and traceability across the full product lifecycle.
Essential Skills
+ Bachelor's degree in Engineering, Quality, Manufacturing, or related technical field.
+ 5+ years of experience in quality assurance, preferably in LED lighting, electronics, or hardware manufacturing.
+ 3+ years of experience in a leadership role managing remote and in-house teams.
+ Strong knowledge of quality tools: Control Plans, FMEA, SPC, 8D, 5 Whys, etc.
+ Experience working with overseas suppliers and managing quality across international supply chains.
+ Familiarity with electrical and optical testing of LED components and systems.
+ Familiarity with UL/ETL certification, RoHS, and CE requirements.
+ Excellent communication and collaboration skills across time zones and cultures.
+ Willingness to travel internationally.
Additional Skills & Qualifications
+ Experience with UL, ETL, and other certification processes for lighting products.
+ Proficiency with ERP or QMS software (Oracle Fusion).
+ Mandarin or other Asian language skills a plus.
Work Environment
At our company, a single team guides a project from concept to manufacturing. Our engineers think holistically about how optics, electronics, aesthetics, and usability interact. Because we make everything we can in-house, every aspect of our products works together flawlessly to deliver realistic, transformative light.
Job Type & Location
This is a Permanent position based out of Carson, California.
Pay and Benefits
The pay range for this position is $ - $ /yr.
health, medical, dental, vision
Workplace Type
This is a fully onsite position in Carson,CA.
Application Deadline
This position is anticipated to close on Oct 15, 2025.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email (% ) for other accommodation options.
Quality Assurance/Supplier Quality Engineering/Quality Control (QA/SQE/QC) Engineer
Posted today
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Job Description
About Us:
Precision Tube & Catheter, Inc. (PT&C) is a high-tech enterprise dedicated to manufacturing advanced materials and components for interventional and implantable medical devices. We produce high-quality medical tubes used in various applications, including anesthesiology, respiratory equipment, and biopharmaceutical laboratory equipment. Our commitment to innovation and excellence drives us to exceed industry standards and client expectations.
Position Summary:
We are a fast-growing startup specializing in the manufacturing of high-performance components for medical catheters, including extruded tubing, shrink tubing, and braided tubing. We are seeking a hands-on and highly motivated Quality Assurance, Supplier Quality Engineering, and Quality Control (QA/SQE/QC) Engineer to lead and execute quality operations and help build a strong foundation for regulatory compliance and product excellence. The QA/SQE/QC Engineer will play a critical role in establishing and maintaining product and process quality. This position will ensure that our products meet or exceed regulatory and customer expectations, support supplier quality management, and oversee in-house quality control activities.
Key Responsibilities:
Quality Assurance (QA) – Process/System-Focused
- Develop and maintain a compliant Quality Management System (QMS) in accordance with ISO 13485 and FDA 21 CFR Part 820.
- Lead internal and external audits; manage CAPA processes and follow-up activities.
- Conduct risk assessments (e.g., PFMEA) and ensure integration of quality in product development and manufacturing.
- Write, revise, and control SOPs, work instructions, forms, and quality records.
- Support equipment and process validations (IQ, OQ, PQ) for tubing manufacturing processes.
- Participate in internal audits, customer audits, and regulatory inspections.
- Manage CAPA processes: initiate, investigate, and implement corrective and preventive actions.
- Collaborate with cross-functional teams (Engineering, Production, R&D) to identify critical-to-quality (CTQ) parameters and ensure product quality.
- Maintain and organize Device History Records (DHRs), Device Master Records (DMRs), and training logs.
Supplier Quality Engineering (SQE):
- Qualify and onboard new suppliers; perform supplier audits and evaluations.
- Define incoming inspection requirements and ensure component conformance.
- Manage supplier non-conformances; initiate and follow through on SCARs.
- Collaborate with suppliers on process improvements and corrective actions.
Quality Control (QC) – Product-Focused
- Perform incoming, in-process, and final inspections of extruded, shrink, and braided tubing.
- Conduct First Article Inspections (FAIs) and maintain inspection records.
- Develop test methods and protocols for product performance and reliability.
- Monitor production quality metrics (e.g., scrap rate, yield, defect rate).
- Maintain and calibrate inspection tools and equipment.
- Use precision measurement tools (micrometers, laser micrometers, pin gauges, tensile testers, etc.).
- Monitor visual and dimensional quality to ensure conformance to specifications and customer requirements.
- Initiate and track Non-Conformance Reports (NCRs) and assist in root cause analysis.
- Maintain calibration logs and ensure metrology equipment is accurate and up-to-date.
Qualifications:
- Bachelor’s degree in Materials Engineering, Quality, or a related technical field.
- 2+ years of experience in a QA/SQE/QC role in the medical device industry preferred.
- Familiarity with catheter manufacturing processes, especially extrusion, shrink tubing, or braiding, is a strong plus.
- Solid understanding of ISO 13485 and FDA QSR (21 CFR Part 820) requirements.
- Experience with quality tools: CAPA, FMEA, 5 Whys, Fishbone Diagram, etc.
- Strong attention to detail, documentation, and organizational skills.
- Hands-on experience with inspection techniques and equipment.
- Ability to thrive in a fast-paced, startup environment.
- Excellent communication, problem-solving, and analytical skills.
Preferred Qualifications:
- Experience with catheter manufacturing processes.
- ASQ certification (CQE, CQA, or equivalent) is a plus.
- Mandarin speaking is a plus
Working Conditions:
Work is performed in a manufacturing environment, requiring adherence to safety protocols.
May involve standing for extended periods and lifting materials as needed.
Benefits / Other:
We believe our employees are our greatest resource. We offer a competitive salary and benefits package including 401(k) with employer contribution, paid holidays, and vacation. Insurance coverage includes medical, dental, vision, and prescription drugs.We are proud to be an equal-opportunity workplace. We are committed to equal employment opportunity regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity, or Veteran status. If you have a disability or special need that requires accommodation, please let us know. If applying for positions in the U.S., you must be eligible to work in the U.S. without needing an employer-sponsored visa (work permit).
Why Join PT&C?
- Be part of a high-impact startup developing critical medical components.
- Work closely with founders and engineers to shape company processes and culture.
- Opportunity for rapid professional growth and ownership in building quality systems from the ground up.
To Apply:
Please submit your resume and cover letter to We look forward to reviewing your application!
Precision Tube & Catheter, Inc. ( ) is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.
Quality Assurance/Supplier Quality Engineering/Quality Control (QA/SQE/QC) Engineer
Posted today
Job Viewed
Job Description
About Us:
Precision Tube & Catheter, Inc. (PT&C) is a high-tech enterprise dedicated to manufacturing advanced materials and components for interventional and implantable medical devices. We produce high-quality medical tubes used in various applications, including anesthesiology, respiratory equipment, and biopharmaceutical laboratory equipment. Our commitment to innovation and excellence drives us to exceed industry standards and client expectations.
Position Summary:
We are a fast-growing startup specializing in the manufacturing of high-performance components for medical catheters, including extruded tubing, shrink tubing, and braided tubing. We are seeking a hands-on and highly motivated Quality Assurance, Supplier Quality Engineering, and Quality Control (QA/SQE/QC) Engineer to lead and execute quality operations and help build a strong foundation for regulatory compliance and product excellence. The QA/SQE/QC Engineer will play a critical role in establishing and maintaining product and process quality. This position will ensure that our products meet or exceed regulatory and customer expectations, support supplier quality management, and oversee in-house quality control activities.
Key Responsibilities:
Quality Assurance (QA) – Process/System-Focused
- Develop and maintain a compliant Quality Management System (QMS) in accordance with ISO 13485 and FDA 21 CFR Part 820.
- Lead internal and external audits; manage CAPA processes and follow-up activities.
- Conduct risk assessments (e.g., PFMEA) and ensure integration of quality in product development and manufacturing.
- Write, revise, and control SOPs, work instructions, forms, and quality records.
- Support equipment and process validations (IQ, OQ, PQ) for tubing manufacturing processes.
- Participate in internal audits, customer audits, and regulatory inspections.
- Manage CAPA processes: initiate, investigate, and implement corrective and preventive actions.
- Collaborate with cross-functional teams (Engineering, Production, R&D) to identify critical-to-quality (CTQ) parameters and ensure product quality.
- Maintain and organize Device History Records (DHRs), Device Master Records (DMRs), and training logs.
Supplier Quality Engineering (SQE):
- Qualify and onboard new suppliers; perform supplier audits and evaluations.
- Define incoming inspection requirements and ensure component conformance.
- Manage supplier non-conformances; initiate and follow through on SCARs.
- Collaborate with suppliers on process improvements and corrective actions.
Quality Control (QC) – Product-Focused
- Perform incoming, in-process, and final inspections of extruded, shrink, and braided tubing.
- Conduct First Article Inspections (FAIs) and maintain inspection records.
- Develop test methods and protocols for product performance and reliability.
- Monitor production quality metrics (e.g., scrap rate, yield, defect rate).
- Maintain and calibrate inspection tools and equipment.
- Use precision measurement tools (micrometers, laser micrometers, pin gauges, tensile testers, etc.).
- Monitor visual and dimensional quality to ensure conformance to specifications and customer requirements.
- Initiate and track Non-Conformance Reports (NCRs) and assist in root cause analysis.
- Maintain calibration logs and ensure metrology equipment is accurate and up-to-date.
Qualifications:
- Bachelor’s degree in Materials Engineering, Quality, or a related technical field.
- 2+ years of experience in a QA/SQE/QC role in the medical device industry preferred.
- Familiarity with catheter manufacturing processes, especially extrusion, shrink tubing, or braiding, is a strong plus.
- Solid understanding of ISO 13485 and FDA QSR (21 CFR Part 820) requirements.
- Experience with quality tools: CAPA, FMEA, 5 Whys, Fishbone Diagram, etc.
- Strong attention to detail, documentation, and organizational skills.
- Hands-on experience with inspection techniques and equipment.
- Ability to thrive in a fast-paced, startup environment.
- Excellent communication, problem-solving, and analytical skills.
Preferred Qualifications:
- Experience with catheter manufacturing processes.
- ASQ certification (CQE, CQA, or equivalent) is a plus.
- Mandarin speaking is a plus
Working Conditions:
Work is performed in a manufacturing environment, requiring adherence to safety protocols.
May involve standing for extended periods and lifting materials as needed.
Benefits / Other:
We believe our employees are our greatest resource. We offer a competitive salary and benefits package including 401(k) with employer contribution, paid holidays, and vacation. Insurance coverage includes medical, dental, vision, and prescription drugs.We are proud to be an equal-opportunity workplace. We are committed to equal employment opportunity regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity, or Veteran status. If you have a disability or special need that requires accommodation, please let us know. If applying for positions in the U.S., you must be eligible to work in the U.S. without needing an employer-sponsored visa (work permit).
Why Join PT&C?
- Be part of a high-impact startup developing critical medical components.
- Work closely with founders and engineers to shape company processes and culture.
- Opportunity for rapid professional growth and ownership in building quality systems from the ground up.
To Apply:
Please submit your resume and cover letter to We look forward to reviewing your application!
Precision Tube & Catheter, Inc. ( is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.
Manufacturing Quality Assurance Technician
Posted 3 days ago
Job Viewed
Job Description
Job DescriptionJob Description
Quality Assurance Technician – Manufacturing (Temporary Assignment)
Location: Torrance, CA
Duration: 3-Month Temporary Assignment
Pay: $25–$28/hour
Are you detail-oriented with a passion for precision? Our manufacturing client is seeking a Quality Assurance Technician to ensure products meet the highest standards of quality and compliance. This role offers hands-on experience with in-process testing, product inspections, and supporting new product launches.
Key Responsibilities:
-
Perform daily in-process and physical testing to verify compliance with quality standards.
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Inspect components and final products, recommending modifications to prevent defects.
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Assist in launching new products by providing testing support and improvement suggestions.
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Utilize precision measuring tools such as calipers, micrometers, verniers, pin gauges, height gauges, radius gauges, protractors, dial indicators, optical comparators, and coordinate measuring machines.
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Read and interpret blueprints, ensuring parts meet specifications.
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Document results and support quality improvement initiatives.
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Operate industrial trucks, forklifts, and man lifts safely; maintain required certifications.
Qualifications:
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1+ year mechanical inspection/calibration experience in manufacturing; plastics processing or product assembly experience a plus.
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Proficient in blueprint reading and measurement standards.
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Intermediate computer skills in Microsoft Word, Excel, and PowerPoint; SAP knowledge .
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Strong problem-solving skills with the ability to analyze causes of failure.
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Ability to work at elevated heights and handle industrial equipment safely.
Interested? Contact Daisy at or email for more information.
Company DescriptionKelly helps companies recruit and manage skilled workers and helps job seekers find great work in industries such as accounting and finance, education, engineering, government, manufacturing and production, technology, and more.
Since inventing the staffing industry in 1946, we’ve become experts in the many specialties and local and global markets we serve. With a network of suppliers and partners around the world, we connect 450,000+ people with work every year. We ensure companies have the people they need, when and where they’re needed most.
Kelly is committed to providing equal employment opportunities to all qualified employees and applicants regardless of , , , , , , , , veteran status, , marital status, , genetic information, or any other legally protected status, and we take affirmative action to recruit, employ, and advance qualified individuals with disabilities and protected veterans in the workforce. Requests for accommodation related to our application process can be directed to the Kelly Human Resource Knowledge Center. Kelly complies with the requirements of California’s state and local Fair Chance laws. A conviction does not automatically bar individuals from employment. Kelly participates in E-Verify and will provide the federal government with your Form I-9 information to confirm that you are authorized to work in the U.S.Company DescriptionKelly helps companies recruit and manage skilled workers and helps job seekers find great work in industries such as accounting and finance, education, engineering, government, manufacturing and production, technology, and more.
Since inventing the staffing industry in 1946, we’ve become experts in the many specialties and local and global markets we serve. With a network of suppliers and partners around the world, we connect 450,000+ people with work every year. We ensure companies have the people they need, when and where they’re needed most.
Kelly is committed to providing equal employment opportunities to all qualified employees and applicants regardless of , , , , , , , , veteran status, , marital status, , genetic information, or any other legally protected status, and we take affirmative action to recruit, employ, and advance qualified individuals with disabilities and protected veterans in the workforce. Requests for accommodation related to our application process can be directed to the Kelly Human Resource Knowledge Center. Kelly complies with the requirements of California’s state and local Fair Chance laws. A conviction does not automatically bar individuals from employment. Kelly participates in E-Verify and will provide the federal government with your Form I-9 information to confirm that you are authorized to work in the U.S.
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Manager, Plasma Quality Assurance
Posted today
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Job Description
Summary:
The Quality Assurance (QA) Manager assures consistent quality of production by developing and enforcing good manufacturing practices (cGMP) systems to ensure overall compliance with operating procedures, regulatory requirements and reports the facility compliance status to Operational and Quality management. This position has primary responsibility for the quality acceptance and release of plasma product shipments and manages the daily activities of the Plasma Logistic Center (PLC) quality assurance staff.
Responsibilities:
Manages the daily activities of the PLC quality assurance staff and ensures that required activities are performed related to the receipt, storage, clearing, processing of lookback alerts, quarantine of unsuitable units, and release of source plasma for further manufacture or sales.
Responsible for the QA release of plasma from PLC and verifies that all shipment contents meet standard operating procedures, regulatory and customer requirements prior to release.
Maintains the PLC deviation management and quality feedback system to notify plasma collection centers (internal and external) of nonconformities noted during the plasma receipt and plasma processing.
Investigates and documents deviations noted as a result of routine compliance reviews, internal and external audits and customer complaints.
Interact with facility management and other members of PLC management to assure understanding of audit findings.
Analyze and evaluate reports prepared by facilities in response to audits performed. Evaluate for adequacy of corrective actions, completeness of report and close audit when satisfactorily completed.
Monitors Plasma Operations in order to maintain compliance with all applicable regulations, both foreign and domestic. Participates in internal audit of the PLC facility.
Leads activities needed to assess facility compliance with SOPs, applicable domestic regulatory agencies such as FDA, international regulatory agencies such as EMA, federal and state regulations. Responsible for coordinating and conducting the Internal Audits at the PLCs.
Participates in the writing and revision of policies and procedures related to the PLC.
Monitors the PLC in order to maintain compliance with all applicable regulations.
Hires quality assurance staff and implements training programs, careeer advancement objectives for quality assurance staff, performs performance appraisals and enacts corrective actions as needed to and including termination.
Meet quality assurance and company financial objectives by monitoring department costs.
Knowledge, Skills, Abilities:
Strong analytical, organizational and interpersonal skills. Extensive knowledge of cGMPs as specified in the CFR/USP and EP Pharmacopeia/ICH and ISO Guidelines. Excellent written/verbal/leadership skills. Must be able to make sound decisions that may affect the quality purity or efficacy or a drug product. Anticipates and identifies problems; analyzes situations; consider alternatives; monitor and evaluates results in a systematic manner. Displays a commitment to quality in terms of people, product and processes. Computer literate, with experience in use of Microsoft applications
Education:
BS degree in Biology, Chemistry or related Science or Engineering.
Experience:
Typically requires a minimum of 5 years of Quality Assurance related experience and 3 years working in pharmaceuticals. Project or technical leadership experience required. Supervisory or management experience preferred.
**Compensation and Benefits:** The estimated pay scale for the Quality Assurance Manager in City of Industry, CA is **$127,500 - $185,000 per year.** Additionally, the position is eligible to participate in up to **8%** of the company bonus pool. We offer a wide variety of benefits including, but not limited to: Medical, Dental, Vision, PTO, up to 5% 401(K) match and tuition reimbursement. Final compensation packages will ultimately depend on education, experience, skillset, knowledge, where the role is performed, internal equity and market data. We are committed to offering our employees opportunities for professional growth and career progression. Grifols is a global healthcare organization with employees in 30 countries focused on patient health and providing impactful results. Since our humble beginnings in 1909, Grifols has been a family company that prides itself on its family-like culture. Our company has more than tripled over the last 10 years, and you can grow with us!
#BiomatUSA
Third Party Agency and Recruiter Notice:
Agencies that present a candidate to Grifols must have an active, nonexpired, Grifols Agency Master Services Agreement with the Grifols Talent Acquisition Department. Additionally, agencies may only submit candidates to positions that they have been engaged to work on by a Grifols Recruiter. All resumes must be sent to a Grifols Recruiter under these terms or they will be considered a Grifols candidate.
**Grifols provides equal employment opportunities to applicants and employees without regard to race; color; sex; gender identity; sexual orientation; religious practices and observances; national origin; pregnancy, childbirth, or related medical conditions; status as a protected veteran or spouse/family member of a protected veteran; or disability. We will consider for employment all qualified applicants in a manner consistent with the requirements of all applicable laws.**
**Location: NORTH AMERICA : USA : CA-City of Industry:USCOI - City of Industry, CA**
Learn more about Grifols ( ID:**
**Type:** Regular Full-Time
**Job Category:** GENERAL MANAGEMENT
Quality Assurance Manager Senior
Posted 2 days ago
Job Viewed
Job Description
Atrius, Distech Controls and QSC are part of the Acuity Intelligent Spaces (AIS) business segment. Our mission is to make spaces smarter, safer and greener through our strategy of connecting the edge with the cloud using disruptive technologies that leverage data interoperability.
Acuity Inc. (NYSE: AYI) is a market-leading industrial technology company. We use technology to solve problems in spaces, light and more things to come. Through our two business segments, Acuity Brands Lighting (ABL) and Acuity Intelligent Spaces (AIS), we design, manufacture, and bring to market products and services that make a valuable difference in people's lives.
We achieve growth through the development of innovative new products and services, including lighting, lighting controls, building management solutions, and an audio, video and control platform. We focus on customer outcomes and drive growth and productivity to increase market share and deliver superior returns. We look to aggressively deploy capital to grow the business and to enter attractive new verticals. Acuity Inc. is based in Atlanta, Georgia, with operations across North America, Europe and Asia. The Company is powered by approximately 13,000 dedicated and talented associates. Visit us at .
**Job Summary**
The Manager, Quality Systems is tasked to lead our quality excellence initiatives and ensure that our products meet the highest standards of quality, reliability, and performance. Responsible for implementing and managing quality systems compliance to ISO standards and utilizing best industry practices for quality in design and supply chain for driving continuous improvement in quality process across the organization. The right person for this role is comfortable in setting and driving step-change improvement and has experience managing quality systems for electronics. The individual applying should be excited to make a difference and bring leading practices to the forefront.
This position will be Hybrid out of our Costa Mesa, CA location.
**Key Tasks & Responsibilities (Essential Functions)**
+ The ideal candidate should be a critical thinker who can assess the current quality management system, identify future state needs against best-in-class standards, and proactively develop and implement an improvement roadmap.
+ Facilitate and maintain quality management systems and ISO-related programs, being the person responsible to manage and maintain ISO 9001, ISO 14001, and any new ISO standard as required (including ensuring ongoing compliance and establishing additional programs as needed).
+ Ensure regulatory compliance for electronics manufacturing, including active management of requirements such as RoHS, REACH, and conflict minerals.
+ Apply strategic planning tools and methods to align the quality vision, mission and goals with the organizational strategy.
+ Implement quality practices in design such as Advanced Product Quality Planning (APQP) and Production Part Approval Process (PPAP) to ensure customer satisfaction and product conformity.
+ Collaborate with suppliers and vendors to ensure the quality of materials and components used in our products.
+ Cross functional coordination with a variety of groups within the organization, such as engineering, manufacturing, sales, customer service, etc., to ensure quality requirements are met throughout core business processes and the product life cycle.
+ Plan and conduct internal and external quality audits, identify potential sources of errors, ineffectiveness, inefficiency, and drive corrective and preventive actions.
+ Monitor and report on key quality indicators, such as customer satisfaction, defect rates, non-conformities, etc. Constant KPI monitoring and drive actions to meet KPI targets.
+ Use statistical techniques and tools to analyze data, monitor processes and improve performance.
+ Ability to work with Agile PLM, Jira, and Power BI. Capable of developing quality dashboards and performing advanced data analysis.
+ Develop and implement quality training programs for staff and provide guidance and support on quality issues.
+ Oversee and coach on root cause analysis, problem solving, and action-plan execution to address CAPAs with cross functional teams.
+ Lead a culture of quality excellence throughout the organization by promoting continuous improvement, customer focus and employee engagement
**Education (minimum education required)**
Bachelor of Engineering
**Skills and Minimum Experience Required**
+ A certification of quality control from ASQ, such as CQE, CQA or CMQ/OE (strongly desired)
+ At least 5 years of experience in quality assurance management or a similar role in electronics. Audio-Video and data network industry desired, but automotive, aerospace, medical or semiconductor industry experience considered transferable.
+ A thorough knowledge of quality assurance methodologies, tools and standards, such as ISO 9001, ISO 14001 , Six Sigma, Lean, APQP, 8D or other structured problem solving, etc.
+ Demonstrates deep expertise in Product Development Processes (PDP), with comprehensive knowledge of quality requirements and standards applicable to each stage of the product life cycle.
+ Experience with Agile PLM, Jira, and Power BI is preferred, including the ability to leverage these tools for process management, issue tracking, and data-driven decision making.
+ Strong analytical and problem-solving skills with the ability to handle complex data.
+ Excellent communication and interpersonal skills with the ability to work effectively with different stakeholders
+ Proven leadership and team-building skills
**Physical Requirements**
+ Light work
**Travel Requirements**
+ 0%
QSC. is owned by Acuity Inc., which is located in the United States. These companies share a global recruitment system on which the data you provide will be stored, and which will be subject to the laws of the United States of America.
**The range for this position is $91,000 to $164,000. Placement within this range may vary, depending on the applicant's experience and geographic location. Acuity offers generous benefits including health care, dental coverage, vision plans, 401K benefits, and commissions/incentive compensation depending on role. For a list of our benefits, click** **here** **.**
We value diversity and are an equal opportunity employer. All qualified applicants will be considered for employment without regards to race, color, age, gender, sexual orientation, gender identity and expression, ethnicity or national origin, disability, pregnancy, religion, covered veteran status, protected genetic information, or any other characteristic protected by law.
Please click here ( and here ( for more information.
**Accommodation for Applicants with Disabilities:** As an equal opportunity employer, Acuity Inc. is committed to providing reasonable accommodations in its application process for qualified individuals with disabilities and disabled veterans. If you have difficulty using our online system due to a disability and need accommodation, you may contact us at . Please clearly indicate what type of accommodation you are requesting and for what requisition.
Any unsolicited resumes sent to Acuity Inc. from a third party, such as an Agency recruiter, including unsolicited resumes sent to an Acuity Inc. mailing address, fax machine or email address, directly to Acuity Inc. employees, or to Acuity Inc. resume database will be considered Acuity Inc. property. Acuity Inc. will NOT pay a fee for any placement resulting from the receipt of an unsolicited resume.
Acuity Inc. will consider any candidate for whom an Agency has submitted an unsolicited resume to have been referred by the Agency free of any charges or fees. This includes any Agency that is an approved/engaged vendor, but does not have the appropriate approvals to be engaged on a search.
E-Verify Participation Poster ( (
Quality Assurance/Supplier Quality Engineering/Quality Control (QA/SQE/QC) Engineer (Irvine)
Posted 1 day ago
Job Viewed
Job Description
About Us:
Precision Tube & Catheter, Inc. (PT&C) is a high-tech enterprise dedicated to manufacturing advanced materials and components for interventional and implantable medical devices. We produce high-quality medical tubes used in various applications, including anesthesiology, respiratory equipment, and biopharmaceutical laboratory equipment. Our commitment to innovation and excellence drives us to exceed industry standards and client expectations.
Position Summary:
We are a fast-growing startup specializing in the manufacturing of high-performance components for medical catheters, including extruded tubing, shrink tubing, and braided tubing. We are seeking a hands-on and highly motivated Quality Assurance, Supplier Quality Engineering, and Quality Control (QA/SQE/QC) Engineer to lead and execute quality operations and help build a strong foundation for regulatory compliance and product excellence. The QA/SQE/QC Engineer will play a critical role in establishing and maintaining product and process quality. This position will ensure that our products meet or exceed regulatory and customer expectations, support supplier quality management, and oversee in-house quality control activities.
Key Responsibilities:
Quality Assurance (QA) Process/System-Focused
- Develop and maintain a compliant Quality Management System (QMS) in accordance with ISO 13485 and FDA 21 CFR Part 820.
- Lead internal and external audits; manage CAPA processes and follow-up activities.
- Conduct risk assessments (e.g., PFMEA) and ensure integration of quality in product development and manufacturing.
- Write, revise, and control SOPs, work instructions, forms, and quality records.
- Support equipment and process validations (IQ, OQ, PQ) for tubing manufacturing processes.
- Participate in internal audits, customer audits, and regulatory inspections.
- Manage CAPA processes: initiate, investigate, and implement corrective and preventive actions.
- Collaborate with cross-functional teams (Engineering, Production, R&D) to identify critical-to-quality (CTQ) parameters and ensure product quality.
- Maintain and organize Device History Records (DHRs), Device Master Records (DMRs), and training logs.
Supplier Quality Engineering (SQE):
- Qualify and onboard new suppliers; perform supplier audits and evaluations.
- Define incoming inspection requirements and ensure component conformance.
- Manage supplier non-conformances; initiate and follow through on SCARs.
- Collaborate with suppliers on process improvements and corrective actions.
Quality Control (QC) Product-Focused
- Perform incoming, in-process, and final inspections of extruded, shrink, and braided tubing.
- Conduct First Article Inspections (FAIs) and maintain inspection records.
- Develop test methods and protocols for product performance and reliability.
- Monitor production quality metrics (e.g., scrap rate, yield, defect rate).
- Maintain and calibrate inspection tools and equipment.
- Use precision measurement tools (micrometers, laser micrometers, pin gauges, tensile testers, etc.).
- Monitor visual and dimensional quality to ensure conformance to specifications and customer requirements.
- Initiate and track Non-Conformance Reports (NCRs) and assist in root cause analysis.
- Maintain calibration logs and ensure metrology equipment is accurate and up-to-date.
Qualifications:
- Bachelors degree in Materials Engineering, Quality, or a related technical field.
- 2+ years of experience in a QA/SQE/QC role in the medical device industry preferred.
- Familiarity with catheter manufacturing processes, especially extrusion, shrink tubing, or braiding, is a strong plus.
- Solid understanding of ISO 13485 and FDA QSR (21 CFR Part 820) requirements.
- Experience with quality tools: CAPA, FMEA, 5 Whys, Fishbone Diagram, etc.
- Strong attention to detail, documentation, and organizational skills.
- Hands-on experience with inspection techniques and equipment.
- Ability to thrive in a fast-paced, startup environment.
- Excellent communication, problem-solving, and analytical skills.
Preferred Qualifications:
- Experience with catheter manufacturing processes.
- ASQ certification (CQE, CQA, or equivalent) is a plus.
- Mandarin speaking is a plus
Working Conditions:
Work is performed in a manufacturing environment, requiring adherence to safety protocols.
May involve standing for extended periods and lifting materials as needed.
Benefits / Other:
We believe our employees are our greatest resource. We offer a competitive salary and benefits package including 401(k) with employer contribution, paid holidays, and vacation. Insurance coverage includes medical, dental, vision, and prescription drugs.We are proud to be an equal-opportunity workplace. We are committed to equal employment opportunity regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity, or Veteran status. If you have a disability or special need that requires accommodation, please let us know. If applying for positions in the U.S., you must be eligible to work in the U.S. without needing an employer-sponsored visa (work permit).
Why Join PT&C?
- Be part of a high-impact startup developing critical medical components.
- Work closely with founders and engineers to shape company processes and culture.
- Opportunity for rapid professional growth and ownership in building quality systems from the ground up.
To Apply:
Please submit your resume and cover letter to We look forward to reviewing your application!
Precision Tube & Catheter, Inc. ( ) is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.