Quality Auditor
$89k - $135.75kavav
Summary The Quality Management and Improvement Internal Auditor is responsible for performing quality management systems audits (product, process, or systems) at several AV locations. Position Responsibilities Provide technical subject matter expertise on the interpretation and usage of standards with AV staff and external audit resources (i.e. 3 party registrars and customers). Communicates, trains, and coordinates improvement of QMS policies, processes, and procedures. Perform periodic audits and engage process owners and resources to identify quality management system risks and compliance with Aerospace standards (i.e. AS9100D) and international standards (i.e. ISO 9001:2015). Engages process owners and leadership in the management and timeliness of corrective and preventive action responses. In addition, evaluate the adequacy of those responses. Engages process owners and leadership in the planning and implementation of auditing activities and participate in continuous improvement activities. Provides governance and oversight to ensure programs are executed within the QMS framework. Maintains problem reporting and CAPA systems for Containment, Correction & Prevention Actions and Documentation of non-conformances (or findings) to the QMS. Leads RCCA of trend-level issues across the QMS. Performs other duties as assigned or required. Basic Qualifications (Required Skills & Experience) Bachelor’s degree in engineering, Quality, or a related technical field (master’s preferred). Minimum 7 years of experience in quality, mission assurance, or regulatory compliance within the defense, aerospace, or high-reliability manufacturing environment. Strong background in AS9100, ISO 9001, ITAR, CMMI, and defense quality standards. Other Qualifications & Desired Competencies CPA/CIA or other certification preferred. Strong communication and influencing skills, with the ability to lead without direct authority. Proven leadership experience managing auditing, compliance teams and cross-functional initiatives. Experience with government contracts, DoD requirements, and working with regulatory agencies. Strong analytical, problem-solving, and project management skills. Lean‑Six‑Sigma and other Continuous Improvement skills. Proficiency with quality tools/software (e.g., Minitab, SPC/QMS platforms, PLM, ERP systems). Preferred Certifications: ASQ Certified Quality Engineer (CQE) or ASQ Certified Quality Manager (CQM); Lean Six Sigma Black Belt or Master Black Belt; Project Management Professional (PMP); Certified Lead Auditor for AS9100/ISO 9001. Displays strong initiative and drive to accomplish goals and meet company objectives. Takes ownership and responsibility for current and past work products. Is committed to learning from mistakes and driven to improve and enhance performance of oneself, others, and the company. Strong background in QMS implementation and risk mitigation strategies. Focuses on teamwork and puts the success of the team above one's own interests. Physical Demands Ability to work in an office or home office environment (Constant). Required to sit and stand for long periods; talk, hear, and use hands and fingers to operate a computer and telephone keyboard (Frequent). Special Requirements U.S. Citizen, U.S. Permanent Resident (Green Card holder), or asylee/refugee status required. May be required to travel within the Continental U.S. and/or abroad. Clearance Level No Clearance Salary range: $89,000 - $135,750 Benefits AV offers an excellent benefits package including medical, dental, vision, 401K with company matching, a 9/80 work schedule and a paid holiday shutdown. For more information about our company benefit offerings please visit: ITAR Requirement This position requires access to information that is subject to compliance with the International Traffic Arms Regulations ("ITAR") and/or the Export Administration Regulations ("EAR"). In order to comply with the requirements of the ITAR and/or the EAR, applicants must qualify as a U.S. person under the ITAR and the EAR, or a person to be approved for an export license by the governing agency whose technology comes under its jurisdiction. Please understand that any job offer that requires approval of an export license will be conditional on AeroVironment’s determination that it will be able to obtain an export license in a time frame consistent with AeroVironment’s business requirements. A “U.S. person” according to the ITAR definition is a U.S. citizen, U.S. lawful permanent resident (green card holder), or protected individual such as a refugee or asylee. See 22 CFR § 120.15. Some positions will require current U.S. Citizenship due to contract requirements. Equal Employment Opportunity Statement We are proud to be an EEO/AA Equal Opportunity Employer, including disability/veterans. AeroVironment, Inc. is an Equal Employment Opportunity (EEO) employer and welcomes all qualified applicants. Qualified applicants will receive fair and impartial consideration without regard to race, sex, color, religion, national origin, age, disability, protected veteran status, genetic data, sexual orientation, gender identity or other legally protected status. U.S. Citizenship required #J-18808-Ljbffr avav
$89.9k - $141.24k
...information I submit in my employment application is true to the best of my knowledge. Job Description About the Role: As a Quality Systems Specialist , you will support the day-to-day execution and continuous improvement of Quality Management System (QMS)...SuggestedMinimum wageFull timeTemporary workWork at officeLocal area$100.45k - $135.9k
...lay within them, you’ll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career.Quality Control Specialist, MicrobiologyWhat you will doLet’s do this. Let’s change the world. In this vital role, you will provide...SuggestedFull timeContract workWork experience placementFlexible hoursWeekend work$91k - $114.2k
Quality Assurance (QA) Specialist III in Camarillo, CABuild your future at Curia, where our work has the power to save lives.The Quality Assurance Specialist III is responsible for maintaining Quality Systems and work cross functionally with Manufacturing, Project Management...SuggestedContract workImmediate start$22 - $32 per hour
...in Life Sciences or related field or the equivalent combination of education and/or experience. Typically 1 plus years of related quality assurance or manufacturing experience in a GMP pharmaceutical or medical device industry. Tasks and Expectations Evaluate documentation...SuggestedSummer work- A national recruiting company is seeking a laboratory technician to perform routine procedures and testing in support of a lab team. The ideal candidate will possess a Bachelor's degree in a science field and have experience in gene expression and cell proliferation methods...Suggested
$104.29k - $141.09k
...Career Category Quality Job Description Join Amgen’s Mission of Serving Patients At Amgen, if you feel like you’re part of something bigger, it’s because you are. Our shared mission—to serve patients living with serious illnesses—drives all that we do. Since 1980, we’ve...Flexible hours- Takeda in Thousand Oaks seeks a Quality Systems Specialist to drive day-to-day QMS activities, ensure compliance, and promote a culture of quality and data integrity. You will be SME for Quality System processes, overseeing deviations, CAPAs, change controls, and supplier...
- ...records in an audit‑ready state Assist with laboratory investigations including OOS results, deviations, invalid assays, and other quality system activities Support laboratory maintenance, calibration, housekeeping, and audit readiness activities Work cross‑functionally...
$40 - $60 per hour
...department. Key responsibilities are to execute analytical method transfers, including raw materials, for use in a cGMP environment in Quality control. You will be responsible for conducting biological or chemical and physical analyses on raw materials, in-process samples,...Hourly payFull timeTemporary workPart timeWork experience placementWork at officeRemote workHome office- ...Job Description Job Description Job Summary: The Quality Specialist is responsible for creating, reviewing, and submitting First Article Inspection Reports (FAIRs) in accordance with AS9102 standards. This role ensures all quality documentation complies with customer...Work at office
$28 - $30 per hour
Payrate $28.00 - $30.00/hr. Summary Company is seeking a Senior Associate, Quality Assurance (MCS) to provide real-time, floor-based QA support at Company’s USTO site. This fully onsite role involves rotating between day and swing shifts every six months, beginning on...Hourly payFull timeWork experience placementLocal areaFlexible hoursDay shiftAfternoon shift$30 - $32 per hour
MCS Senior Associate Quality Assurance with GMP and Audit Experience (Onsite Job in Thousand Oaks, CA) Location: Thousand Oaks, CA Employment Type: Contract (W2) Duration: 12 months (possible extension) Work Hours: 8:00 AM - 5:00 PM standard; Overtime possible during...Contract work- Amgen is hiring a Specialist Quality Assurance to provide quality systems expertise and lead QA tasks across clinical and commercial products. You will review and approve product quality records, manage deviations/CAPAs, and support change control processes in GMP systems...
- Amgen in Thousand Oaks, CA is seeking a Senior Associate Quality Assurance to join our onsite team. The role focuses on sampling and inspection of raw materials and components, reviewing quality documentation, and supporting continuous improvement projects. Candidates should...
- SSi People is looking for an MCS Senior Associate Quality Assurance in Thousand Oaks, California. This role requires delivering real-time quality assurance support in a drug substance production facility. Responsibilities include providing compliance support and overseeing...Shift work
- ...complaints. Candidates should hold a Bachelor's Degree in Life Sciences or a related field, with at least 1 year of experience in quality assurance or manufacturing in a GMP environment. Strong attention to detail, project management skills, and proficiency in word processing...
- Amgen is seeking a Senior Associate Quality Assurance in Thousand Oaks, CA, to oversee Drug Product manufacturing and ensure adherence to quality processes. The ideal candidate will have a strong background in GMP, effective communication skills, and the ability to support...
- Summary Will work as part of cross-functional teams providing quality oversight, review, and approval of validation deliverables and change controls to ensure that products and processes meet appropriate regulatory agency validation requirements, internal company standards...
- The Judge Group is seeking a detail-oriented Supply Chain Associate to support supply chain, warehouse, manufacturing, and quality operations within a pharmaceutical environment. The role emphasizes GMP/GDP compliance, documentation in CDOCS, and use of DQMS/QMTS. You will...
- Merck & Co. is seeking a Senior Associate, Quality Assurance (MCS) to provide real-time, floor-based QA support at the USTO site. This fully onsite role rotates between day and swing shifts every six months, starting on day shift for training, and focuses on Drug Substance...Day shiftAfternoon shift
- ...lead product is an innovative solution to provide oxygen to tissues. Check us out at We are looking for a motivated and hands-on Quality Operations Specialist to join our team. How you will add value to 20BLOC The Quality Operations Specialist supports the Quality Assurance...Full timeVisa sponsorshipWork visaMonday to Friday
$76.41k - $94.38k
...QC Analyst. Location: Westlake Village, CA. What you’ll do Review complaints for compliance and accuracy. Audit monthly complaint quality, sub‑servicer functions, and internal complaint operations. Evaluate complaint documentation and records for adherence to procedures...- USDM Life Sciences is seeking a QC Analyst to support the QC department in a cGMP environment. You will conduct analyses on raw materials, in-process and final product samples, and environmental monitoring samples. You will drive new methodologies in QC, assist investigations...
- ...department. Key responsibilities are to execute analytical method transfers, including raw materials, for use in a cGMP environment in Quality control. You will be responsible for conducting biological or chemical and physical analyses on raw materials, in-process samples,...Work experience placementWork at officeLocal areaShift workWeekend work
- ...process samples, drug substances, and final products, ensuring timely and accurate data documentation. The role requires 2+ years in quality operations, strong problem-solving skills, and effective communication within a team. Calibration, SOP drafting, and adherence to...
- A leading consulting firm in California is seeking a Senior Associate, Quality Assurance to oversee Drug Substance manufacturing areas and ensure compliance within a GMP environment. The role involves real-time QA support, along with responsibilities like batch record review...Full timeContract work
- A biopharmaceutical company in Thousand Oaks, California is seeking a Quality Operations Specialist. The role encompasses ensuring GMP compliance, supporting batch documentation review, and collaborating with cross-functional teams. Ideal candidates will have a Bachelor...Full time
$30 - $37 per hour
...Job Description Job Description Job Title: Supplier Quality Associate Job Description The Supplier Quality Associate supports the integrity of the Approved Supplier List by aligning data between the Quality Management System (QMS) and Enterprise Resource Planning...Contract workTemporary workFor contractorsWork at office$40.45 per hour
...QC Due Diligence Compliance Analyst As a Quality Control Compliance Analyst, you'll be responsible for auditing the documentation for loans funded and/or purchased by AmeriHome for compliance with Federal, State, County, and/or City regulatory requirements to ensure...Hourly payWork at office$40.45 per hour
...funded and/or purchased by AmeriHome to ensure compliance with federal, state, county, and city regulatory requirements and investor quality standards. Review the validity of defects cited by third‑party diligence firms so that loans meet investor quality standards....Hourly payWork at office
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