quality assurance auditor

City National Bank of Florida

<div>
 
 About Us
 
 
 
 Think BIG. Achieve More.
 
 
 At City National Bank of Florida, we invest in our people and the communities we serve. Join a team where ambitious careers and meaningful relationships thrive together. We&rsquo;re entrepreneurs at heart&mdash;growing fast, making an impact, and shaping the future of banking in Florida. To learn more about City National Bank of Florida visit About Us!
 
 
 
 Overview
 
 
 
 
 About the Role
 
 
 
 The Quality Assurance Auditor is responsible for overseeing and enhancing the quality and performance of the bank's internal audit function. This position is integral in ensuring that internal audit processes consistently meet the highest standards of quality and compliance, in alignment with both regulatory requirements and internal policies. The auditor will be instrumental in driving continuous improvement initiatives, pinpointing areas for enhancement within the audit function, and ensuring the effectiveness of audit procedures. Responsibilities include evaluating compliance with laws, regulations, and operating procedures, assessing the adequacy of procedures for asset protection, and advancing operational quality and efficiency. This role demands a high level of initiative, discretion, and independent judgment, particularly in matters of significant importance to the bank.
 
 
 
 What You'll Do
 
 
 
 <ul>
 <li>
 Oversees the internal audit quality assurance program to ensure audits are performed in accordance with internal audit standards and industry best practices.
 </li>
 <li>
 Develops and implement methodologies, tools, and procedures to monitor and assess the quality of internal audits.
 </li>
 <li>
 Conducts regular quality assessments of audit engagements, identifying areas for improvement.
 </li>
 <li>
 Ensures that all audit activities comply with regulatory requirements, professional standards, and internal policies.
 </li>
 <li>
 Coordinates with regulatory bodies during inspections and audits.
 </li>
 <li>
 Prepares and presents QA reports to senior management and the Audit Committee.
 </li>
 <li>
 Communicates audit findings, quality issues, and recommendations for improvement to the internal audit team.
 </li>
 <li>
 Acts as liaison between internal audit and external auditors/regulators.
 </li>
 <li>
 Identifies and implements best practices in audit quality assurance.
 </li>
 <li>
 Develops and delivers training programs to enhance the skills and knowledge of the internal audit team.
 </li>
 <li>
 Drives initiatives to enhance the effectiveness and efficiency of audit processes and methodologies.
 </li>
 <li>
 Collaborates with the quality assurance team at head office to ensure alignment between audit activities and the bank's overall audit strategy.
 </li>
 <li>
 Contributes to the identification and mitigation of risks associated with the audit function.
 </li>
 <li>
 Assesses the effectiveness of audit tools and technology used in the audit process and recommend improvements as necessary.
 </li>
 <li>
 Engages with various internal stakeholders to understand their perspectives on audit quality and incorporate their feedback into quality assurance activities.
 </li>
 <li>
 Tracks and reports on key quality metrics and performance indicators related to the internal audit function.
 
 
 </li>
 </ul>
 
 Qualifications
 
 
 
 
 What You Bring
 
 
 
 <ul>
 <li>
 5-7 years of experience in internal auditing, audit quality assurance, or a related field.
 </li>
 <li>
 Demonstrated experience in assessing audit processes, ensuring compliance, and implementing quality improvement initiatives.
 </li>
 <li>
 Strong analytical and problem-solving skills with a keen attention to detail.
 </li>
 <li>
 High level of initiative, discretion, and independent judgment.
 </li>
 <li>
 Ability to manage multiple tasks and prioritize effectively in a fast-paced environment.
 </li>
 <li>
 Strong organizational skills with the ability to drive initiatives and collaborate across teams.
 </li>
 <li>
 Proficient in fact-finding, analysis, problem-solving, and decision-making.
 </li>
 <li>
 In-depth knowledge of regulatory requirements, risk frameworks, and guidelines governing credit, liquidity, interest rate, and fiduciary risks.
 </li>
 <li>
 Commitment to continuous professional development and staying updated on emerging trends and changes in audit standards and regulations.
 </li>
 <li>
 Advanced PC skills, including working knowledge of TeamMate, Microsoft Word, and Excel.
 </li>
 <li>
 Experience in creating process documentation, developing audit plans, and performing audits.
 </li>
 <li>
 Ability to plan, execute, and evaluate audit test plans within a risk-based audit methodology.
 </li>
 <li>
 Strong written and verbal communication skills.
 </li>
 <li>
 Knowledge of internal controls, financial terminology, and bank documentation requirements.
 </li>
 <li>
 Experience in assessing financial models, testing their effectiveness, and recommending improvements.
 </li>
 <li>
 Ability to communicate effectively with various levels of staff and management.
 </li>
 <li>
 Ability to manage scheduling and meet deadlines.
 
 
 </li>
 </ul>
 
 Licenses &amp; Certifications
 
 
 
 <ul>
 <li>
 Certified Internal Auditor (CIA), Certified Public Accountant (CPA), Certified Information Systems Auditor (CISA), Certified Fraud Examiner (CFE), Certified Risk Management Assurance (CRMA), Certified Government Auditing Professional (CGAP), Chartered Accountant (CA), Accredited in Business Valuation (ABV), These credentials are advantageous but not mandatory for the role.
 
 
 </li>
 </ul>
 
 Education
 
 
 
 <ul>
 <li>
 Bachelor's Degree in Accounting, Finance, Business Administration, or related field.
 </li>
 <li>
 Master's Degree in Accounting, Finance, Business Administration, or related field.
 </li>
 <li>
 An equivalent combination of education and/or relevant professional experience may be considered in lieu of a degree.
 
 
 </li>
 </ul>
 Benefits &amp; Perks
 
 
 We offer a competitive benefits package designed to support your success:
 
 
 <ul>
 <li>
 Health Coverage: Medical, dental, and vision plans with employer contributions.
 </li>
 <li>
 Retirement Savings: 401(k) with matching.
 </li>
 <li>
 Paid Time Off &amp; Holidays: Generous PTO and paid holidays.
 </li>
 <li>
 Wellness Support: Access to mental health and financial wellness resources.
 
 
 </li>
 </ul>
 Visit our benefits page to learn more Benefits!
 
 
 Join City National Bank of Florida. The possibilities are endless.
 
 
 
 Special Information To Candidates
 
 
 
 City National Bank of Florida is an Equal Opportunity Employer and is committed to providing equal employment opportunities to all applicants. We do not discriminate on the basis of race, color, religion, sex, pregnancy, national origin, age, disability, genetic information, protected veteran status, or any other status protected under federal, state, or Florida law. City National Bank of Florida complies with the Americans with Disabilities Act (ADA) and applicable Florida laws. Qualified individuals with disabilities who require a reasonable accommodation in order to complete the online application or participate in the hiring process may contact our Human Resources Talent Attraction Department talent.attraction@citynational.com.
</div>

Quality Assurance Auditor

Reformation

<div>
 
 Who We Are:
 
 
 
 
 Being naked is the #1 most sustainable option. We're #2.
 
 
 
 Since 2009, we've been on a mission to bring sustainable fashion to everyone. Named one of
 
 Fast Company&rsquo;s Brands That Matter
 
 and winning a
 
 Best Carbon Footprint
 
 award, we have big goals like being
 
 Climate Positive by 2025
 
 ,
 
 Circular by 2030
 
 , and pushing the whole industry forward along the way. Our work has gotten love in
 
 Drapers
 
 and
 
 Sourcing Journal
 
 , and
 
 TIME
 
 wrote about how great our CEO, Hali Borenstein, is. Basically, we're saving the Earth and looking damn good doing it.
 
 
 We're a global brand with 50+ stores (and counting) around the world, and our own
 
 sustainable factory in LA
 
 . We innovate across categories like
 
 accessories
 
 ,
 
 swimwear
 
 , and
 
 sleepwear
 
 , and we reach millions of people with campaigns like
 
 this
 
 ,
 
 this
 
 and
 
 this
 
 .
 
 
 None of this work is possible without the incredible people behind it. We're a mission-based company that invests in an inclusive culture, so we can innovate together and ensure everyone has the space to grow, thrive, and belong.
 
 
 And starting right now, we want to do all that
 
 with you.
 
 
 
 
 Work Location/ Schedule:
 
 Full time, onsite out of Vernon HQ in Los Angeles, CA
 
 
 
 The Role:
 
 
 Quality Assurance Auditor
 
 
 
 The Quality Assurance Auditor is responsible for inspecting work-in-progress, finished garments, and returned merchandise within the facility to ensure they meet company quality standards and specifications. This role plays a key part in maintaining product consistency and supporting internal teams with quality-related issues.
 
 
 
 What you&rsquo;ll do:
 
 
 
 <ul>
 <li>
 Conduct inspections of factory TOPs (Top of Production samples) as assigned.
 </li>
 <li>
 Perform in-line inspections on garments during various production stages.
 </li>
 <li>
 Conduct final audits, including visual inspections and verification of measurement of finished goods.
 </li>
 <li>
 Identify, document, and recommend corrective actions for quality issues found during inspections.
 </li>
 <li>
 Inspect returned merchandise to determine defect types and root causes.
 </li>
 <li>
 Support internal teams by providing quality-related feedback and guidance.
 </li>
 <li>
 Collaborate with other QC auditors to share insights and standardize inspection approaches.
 </li>
 <li>
 Assist production teams by coaching on quality standards during inspections and sample reviews.
 </li>
 <li>
 Accurately complete inspection reports and input data into relevant systems or templates.
 </li>
 <li>
 Perform additional quality-related tasks as assigned by management.
 
 
 </li>
 </ul>
 
 What you&rsquo;ll need:
 
 
 
 <ul>
 <li>
 High School Diploma or equivalent (GED or High School Equivalency Certificate) required
 </li>
 <li>
 1&ndash;3 years of experience in garment construction and/or apparel manufacturing
 </li>
 <li>
 1&ndash;3 years of quality control experience in the apparel industry
 </li>
 <li>
 Strong organizational, planning, and communication skills
 </li>
 <li>
 High attention to detail and accuracy
 </li>
 <li>
 Team player with good interpersonal skills
 </li>
 <li>
 Ability to read and use a tape measure with precision
 </li>
 <li>
 Solid understanding of garment measuring, construction, and defect identification
 </li>
 <li>
 Knowledge of woven and knit fabrics, garment production, and finishing processes
 </li>
 <li>
 Familiarity with apparel quality control/assurance methods
 </li>
 <li>
 Ability to prepare and interpret product specification sheets
 </li>
 <li>
 Proficiency in Microsoft Word, Excel, and Outlook
 </li>
 <li>
 Ability to read, write, and communicate effectively in English
 </li>
 <li>
 Bilingual (English/Spanish) preferred
 </li>
 <li>
 Ability to lift and carry up to 20&ndash;50 lbs over short distance
 </li>
 <li>
 Capable of performing repetitive hand/wrist motions
 </li>
 <li>
 Able to stand for extended periods, bend, kneel, squat, reach, and move garments or boxes as needed
 
 
 </li>
 </ul>
 
 Compensation:
 
 
 
 At Reformation, we believe in transparency and equity when it comes to compensation. For this role, the anticipated base hourly range is
 
 $20 - $23 an hour
 
 , depending on a variety of factors, including but not limited to relevant experience, skills, qualifications, and internal compensation equity.
 
 
 This role may also be eligible for an annual discretionary bonus based on a range of factors, including company performance, department goals, and individual contributions. Bonus amounts and eligibility are not guaranteed and are determined at the company&rsquo;s discretion.
 
 
 Please note that compensation decisions are made thoughtfully and may vary from the listed range to reflect individual circumstances and evolving business needs. Our total rewards package also includes benefits, perks, and opportunities for growth that contribute to overall compensation.
 
 
 
 Benefits &amp; Perks:
 
 
 
 <ul>
 <li>
 Eligible employees get employer-sponsored private medical, dental, and vision insurance, as well as commuter benefits to help support your travel to and from work.
 </li>
 <li>
 We offer competitive paid time off policies including vacation, sick leave, and company holidays for eligible employees.
 </li>
 <li>
 We offer retirement planning support for eligible employees, including the option to invest in Environmental Social Governance-aligned (fancy way to say sustainable) funds.
 </li>
 <li>
 We&rsquo;re a mission-based company with offices in LA, NYC and London, as well as a global retail team, which means you&rsquo;ll get to collaborate with people all around the world.
 </li>
 <li>
 You&rsquo;ll get access to fertility care support through Carrot, and up to a $5,000 USD reimbursement for related fertility expenses after 1 year of employment.
 </li>
 <li>
 We care about the causes our employees care about so we donate to community efforts on a yearly basis.
 </li>
 <li>
 We offer a clothing discount, culture events (like our annual Ref Values week and Volunteer Time Off), you know, all the meaningful and fun stuff!
 
 
 </li>
 </ul>
 
 
 Reformation is proud to be an Equal Opportunity Employer.
 
 
 
 We&rsquo;re committed to building a diverse and inclusive team that reflects the world we want to live in. All qualified applicants will be considered for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, disability, age, or veteran status&mdash;in accordance with applicable international, federal, state, and local laws.
 
 
 
 
 If you require accommodations during the application or interview process, please let us know. We&rsquo;re here to ensure you have what you need to show up as your best self.
 
 
 
 
 
 Still don&rsquo;t know if you should apply?
 
 
 
 We get it&mdash;
 
 
 
 studies
 
 
 
 show that many women and individuals from historically underrepresented communities hold back from applying unless they meet every single requirement. At Reformation, we&rsquo;re all about growth, not gatekeeping. If you&rsquo;re passionate about the role and excited about making fashion more sustainable, we&rsquo;d love to hear from you. If this role doesn&rsquo;t totally excite you, consider applying to our
 
 
 
 general application.
 
 
 
 
 
 Want some more?! -
 
 
 Sustainability
 
 ,
 
 Forbes
 
 
 ,
 
 
 Fast Company
 
 
 
 
 California Applicant Privacy Notice
 
 
 found here
 
</div>

Insurance Institute for Business and Home Safety

<div>The Insurance Institute for Business &amp; Home Safety (IBHS) is looking for a meticulous and knowledgeable FORTIFIED Quality Assurance Auditor to join our team. In this role, you will ensure that structures certified under the FORTIFIED program meet the highest standards of resilience and quality. Your work will directly contribute to enhancing the durability and safety of homes and businesses against severe weather threats. The ideal candidate will have a strong understanding of construction practices and quality assurance processes, combined with a commitment to promoting building resilience through rigorous inspections and audits. 
Responsibilities<ul><li>
Conduct on-site inspections and audits of construction projects to verify compliance with FORTIFIED program standards and guidelines.</li><li>
Review documentation and reports submitted by builders and contractors to ensure accuracy and completeness.</li><li>
Identify and document any discrepancies, deficiencies, or areas of non-compliance, and communicate these effectively with relevant stakeholders.</li><li>
Collaborate with builders, contractors, and program administrators to provide guidance and support for meeting FORTIFIED standards.</li><li>
Maintain detailed records of all inspections, audits, and communications related to the quality assurance process.</li><li>
Stay current with updates to FORTIFIED standards, building codes, and industry best practices.</li><li>
Participate in training sessions and contribute to the continuous improvement of audit procedures.</li><li>
Report findings and provide recommendations to improve program implementation and effectiveness.</li></ul> 

Requirements 
<ul><li>
High school diploma or equivalent required; Associate or Bachelor&rsquo;s degree in construction management, engineering, or a related field preferred.</li><li>
Minimum of 3 years&rsquo; experience in construction, building inspection, or quality assurance roles.</li><li>
Strong knowledge of residential and commercial building codes, construction practices, and FORTIFIED program standards.</li><li>
Detail-oriented with excellent observational and documentation skills.</li><li>
Effective communication skills to interact with builders, contractors, and stakeholders.</li><li>
Ability to work independently in the field and manage multiple inspections efficiently.</li><li>
Valid driver&rsquo;s license and reliable transportation.</li><li>
Certification related to building inspection or quality assurance is a plus.</li></ul> 

Benefits 
<ul><li>
Health Care Plan (Medical, Dental &amp; Vision)</li><li>
Retirement Plan (401k, IRA)</li><li>
Life Insurance (Basic, Voluntary &amp; AD&amp;D)</li><li>
Paid Time Off (Vacation, Sick &amp; Public Holidays)</li><li>
Family Leave (Maternity, Paternity)</li><li>
Short Term &amp; Long Term Disability</li><li>
Training &amp; Development</li></ul></div>

FORTIFIED Quality Assurance Auditor

Colorcon

<div><div><div>Quality Assurance Auditor I (Indy)</div></div><div><div><div>
Indianapolis, IN, United States</div><div><div>
|</div></div><div>
req545</div></div></div><div></div><div><div><div><div> 
</div></div></div></div><div><div><div>
Posted on: 4/13/2026</div></div></div></div>
 <div>Quality Assurance Auditor I (Indy)
 Colorcon&reg; is a world leader in the development, supply and technical support of formulated film coating systems, modified release technologies, specialty excipients and functional packaging for the pharmaceutical, nutritional, and animal health industries. Our best-in-class products and technologies are complemented by our extensive formulation experience, application data and value-added services to support all phases of solid oral dose design, development, and manufacture.
Our focus on market issues and technology development has earned Colorcon an international reputation as a pharmaceutical supplier of choice. That reputation is based on superior product quality, unparalleled technical support, extensive regulatory assistance and reliable supply from multiple locations, with our Global Headquarters located in Harleysville, Pennsylvania. 
Colorcon has 26 technical service laboratories globally and more than 2100 employees exclusively dedicated to its customer base. 
We are a successful company thanks to our diverse workforce and global reach. We believe that our operating principles define our culture, values and organizations and are key to achieving our mission and vision, strategies and goals.
Platinum Rule: We treat others the way they want to be treated 
Empowerment: We trust our colleagues with responsibility and decision-making 
Keep Getting Better: We create an environment for constant improvement, to be the best we can 
Teamwork: We embrace the value of collaboration; work together to exceed what is possible as individuals 
Customer Focus: We put our customers&rsquo; needs at the heart of everything we do 
Global Respect: We are citizens of a diverse world and behave with respect for the communities in which we operate
Our People Enjoy a Wide Offering of Employee Benefits, including but not limited to:<ul><li>
All employees are eligible to participate in our company-wide bonus program 
</li><li>
Employees have the choice between three medical plans 
</li><li>
100% company-paid Dental Insurance for all employees and their qualifying dependents 
</li><li>
Optional Vision Coverage 
</li><li>
Fitness and Wellness Programs 
</li><li>
Employee Assistance Programs (EAP) 
</li><li>
Corporate Social Responsibility Groups (CSR) 
</li><li>
Parental Leave 
</li><li>
Tuition Reimbursement; up to $8,000 per calendar year 
</li><li>
401(k) Company Matching</li><li>
Paid Time Off</li><li>
Paid Holidays</li></ul>
Colorcon is committed to maintaining a diverse workforce and an inclusive and equitable work environment. This includes all employment-related decisions and business dealings on the basis of race, color, ethnicity, national origin, age, sex, sexual orientation, religion, disability, veteran status, or any other legally protected status.<div>
Position Summary 
The Quality Assurance (QA) Auditor I is responsible for batch review and release and assists in investigation of reported product quality issues and internal non-conformance issues. The QA Auditor I is also responsible for meeting all other tasks assigned via their yearly goals set by the Quality Supervisor. The position reports to the Quality Supervisor. 
 
Responsibilities &amp; Duties 
<ul><li>Aware of GMPs and GLPs and maintains compliance with those regulations</li><li>Performs batch review and product release activities for the Indianapolis site</li><li>Prepares paperwork for samples being sent to the QC laboratory.</li><li>Supports sending samples for external testing.</li><li>Assists with internal quality audits</li><li>Perform quality review/audit of incoming raw materials and finished products.</li><li>Supports the investigation of customer reported product quality issues, internal non-conformance (INC) issues and other manufacturing deviations or problems.</li><li>Partners with quality control, operations, engineering, maintenance, safety and supply chain to ensure appropriate and timely determination of scope, product impact, root cause and corrective actions of product quality issues, INC issues and other manufacturing deviations.</li><li>Fosters collaborative relationships focused on high quality investigations, meaningful corrective actions and the reduction of INC issues.</li><li>Documents all investigation activities in detailed, timely reports utilizing Colorcon&rsquo;s Customer Support Solution (CSS).</li><li>Responsible for initiating INC service Requests (SRs)</li><li>Issue necessary quality paperwork for SR related operations.</li><li>Assists with new hire training for employees</li><li>Assists with document retention.</li></ul></div><div>
Requirements 
<ul><li>Bachelor&rsquo;s degree in a physical science preferred or a minimum of 2 years quality auditing experience required.</li><li>Ability to work comfortably in the manufacturing area.</li><li>Ability to communicate effectively at all levels verbally and in written reports.</li><li>Experience in technical writing strongly preferred.</li><li>Consistent attention to detail.</li><li>Excellent organizational and decision-making skills.</li><li>Prior experience in problem solving techniques highly desirable.</li></ul></div> 
Location: 
3702 E. 21st St. 
Indianapolis, Indiana, 46218 
United States 
 
Colorcon 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. If E-Verify cannot confirm that you are authorized to work, this employer is required to give you written instructions and an opportunity to contact Department of Homeland Security (DHS) or Social Security Administration (SSA) so you can begin to resolve the issue before the employer can take any action against you, including terminating your employment. Employers can only use E-Verify once you have accepted a job offer and completed the Form I-9. 
E-Verify Works for Everyone 
For more information on E-Verify, or if you believe that your employer has violated its E-Verify responsibilities, please contact DHS.</div>

Quality Assurance Auditor I (Indy)

Intertek

<div></div><div>Medical Device Auditors - Full-time - Travel based Auditor.
Interested in future career opportunities in the Quality Assurance audit and support services industry? We're looking for a Medical Device Auditor that wants to build something great with an incredible group of people. By joining Intertek, your contributions will be valued as we continue to help the world Build Back Ever Better.
Intertek's Business Assurance team goes beyond testing, inspection and certification to look at the underlying elements that make a company and its products successful. Our assurance solutions provide confidence and total peace of mind that a client's operating procedures, systems and people are functioning properly to provide a competitive advantage in the marketplace.
What are we looking for?
The Auditor, Medical Devices will support the Business Assurance business by leading and/or participating as an assessor during all phases of a client&rsquo;s management system, in accordance with the company&rsquo;s accredited certification program. The Auditor is the primary interface with the client before and during the process of all auditing activities. Additionally, the Auditor will help train low-graded Auditors through witness audits, technical support, and education of both client and sales force as needed.
This will be a travel-based position, with extensive travel to client sites required. Candidate must be comfortable traveling 3 to 5 nights per week. This is a remote position; however, applicants must reside in and be able to legally work in the United States.
Salary &amp; Benefits Information
Individual compensation packages are based on a variety of factors unique to each candidate including skill set, experience, qualifications, and other job-related reasons.
In addition to competitive compensation packages, when working with Intertek you can expect benefits including medical, dental, vision, life, disability, 401(k) with company match, generous vacation / sick time (PTO), tuition reimbursement and more.
What you&rsquo;ll do:<ul><li>
Audit client management systems for compliance with established standards, client, and/or industry requirements, government regulations, and other relevant standards, specifically ISO 13485, regulatory requirements for the US, Canada, Japan, Australia, and/or Brazil, and/or GMP regulatory requirements related to the medical device, pharmaceutical and/or cosmetic industry.</li><li>
Assist clients with questions relevant to the audit and/or certification process.</li><li>
Act as Lead Auditor or team member.</li><li>
Travel will include overnight 3 to 5 days per week, to various worksites and client locations .</li><li>
Coordinate audit activity with team members.</li><li>
Liaison with client regarding audit activity.</li><li>
Review client's quality management system documentation</li><li>
Verify and document evidence of compliance and non-compliance.</li><li>
Prepare audit report.</li><li>
Review audit results with coordinator and other assessment team members. Make presentations to clients and/or certification board concerning audit results, when required.</li><li>
Assist with corrective action requirements resulting from assessments.</li><li>
Participate in audit meetings.</li><li>
Review audit reports and provide technical assistance to the medical team.</li><li>
Support management in areas of continuous improvement.</li><li>
Provide management with updates on status of work, initiatives, and projects, as required.</li></ul>
This position outline is a general guideline and does not represent all encompassing details. The position assumes that the incumbent has both the mental and physical requirements to carry out the above defined duties.
Minimum Requirements &amp; Qualifications:<ul><li>
4 year college/university degree in a science or technical field (biology or microbiology; chemistry or biochemistry; computer and software technology; electrical, electronic, mechanical or bioengineering; human physiology; medicine; pharmacy; physics or biophysics) or equivalent combination of relevant education and work experience.</li><li>
A minimum of 4+ years of full-time work experience in a medical device or related medical device industry (design, development, testing, quality assurance/quality control).</li><li>
A minimum of 2+ years in a quality management systems environment (auditing, CAPA, complaints, management review)</li><li>
Completed Lead Auditor training for any standard (preferably ISO 13485 and/or relevant regulatory requirements), but will train if needed.</li><li>
Strong communication and interpersonal skills.</li><li>
Sound judgment, organizational, and analytical skills.</li><li>
Excellent computer and writing skills.</li><li>
Ability to define problems, collect data, establish facts, and draw valid conclusions.</li><li>
Ability to exercise effective time management skills in completion of assignments.</li><li>
Must be willing and able to travel extensively. Primarily domestic travel, some international travel may be needed (typically includes USA+Canada+Mexico).</li><li>
Possess a valid unrestricted driver&rsquo;s license and the ability to operate a motor vehicle in the performance of the official duties of the position.</li></ul>
Preferred Requirements &amp; Qualifications:<ul><li>
Lead Auditor Training with (ISO19011 OR ISO13485) Certification</li><li>
Related 3rd party auditing industry management systems experience.</li><li>
Working knowledge of relevant regulatory requirements for medical devices and pharmaceuticals in the EU, US, Australia, Japan, Brazil, and/or Canada.</li><li>
Experience implementing/auditing to ISO 13485, ISO 14971, and medical device regulatory requirements.</li><li>
Device Industry experience with Orthopedic implants, Active devices, Software as a medical device, Monitoring devices, IVF and ART devices, and sterility requirements (ETO, GAMMA).</li><li>
Specific experience/training on processes used in the relevant industry&rsquo;s manufacturing (ex. sterilization, machinery, electric and electronic devices or components, software development).</li><li>
Training/experience in quality tools (Kaizen, lean manufacturing, etc.).</li></ul> 
PHYSICAL REQUIREMENTS:
This role requires the ability to:<ul><li>
Ascend or descend ladders, stairs, ramps, and the like, using feet and legs and/or hands and arms. Body agility is emphasized.</li><li>
Stand, for sustained periods of time.</li><li>
Walk, moving on foot to accomplish tasks and to move from one work location to another.</li><li>
Communicate well, thru spoken word, conveying detailed accurate information &amp; instructions to others.</li><li>
Hear well, perceiving sounds with or without correction, including the ability to receive information thru oral communications.</li><li>
Exert up to 10 pounds of force occasionally and/or negligible amounts of force frequently to lift, carry, push, pull or otherwise move objects.</li><li>
Have close visual acuity to perform an activity such as preparing &amp; analyzing data, viewing a computer monitor, reading, report writing, visual inspection, and use of measurement devises.</li></ul>
Intertek: Total Quality. Assured.
Intertek is a world leader in the Quality Assurance market, with a proven, high-quality business model and a global network of customer-focused operations and highly engaged subject matter experts. With passion, pace, and precision we work to exceed our customers&rsquo; expectations, while engaging with our employees to be 10X in their performance and professional growth.
Intertek is a drug-free workplace. As a condition of employment, certain positions may be required to pass a pre-employment drug test based on the type of work that will be performed.
We Value Diversity
Intertek&rsquo;s network of phenomenal people are our greatest assets, and the diversity they bring fuels our success. Intertek is an Equal Employment Opportunity Employer that values inclusion and diversity. We take affirmative action to ensure all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, or other legally protected characteristics.
For individuals with disabilities who would like to request accommodation, or who need assistance applying, please email intertekhrusa@intertek.com or call 1-877-694-8543 (option #5) to speak with a member of the HR Department. 
#LI-Remote
#LI-JC1<ul><li>Intertek does not accept unsolicited approaches from agencies and will not pay a fee for any placement resulting from the receipt of an unsolicited resume.
</li></ul>The Business Assurance group of Intertek provides a full range of business process audit and support services, including management systems certification, sustainability and responsible sourcing audits, risk management, and training. Our range of bespoke auditing, performance benchmarking and supply chain solutions provide insight into every aspect of operations, allowing clients to make informed decisions about their business while ensuring their workforce competencies are current and relevant.Intertek is a leading Total Quality Assurance provider to industries worldwide. Our network of more than 1,000 laboratories and offices in more than 100 countries, delivers innovative and bespoke Assurance, Testing, Inspection and Certification (ATIC) solutions for our customers' operations and supply chains. Working at Intertek means joining a global network of state-of-the-art facilities and passionate people who deliver superior customer service with a purpose of bringing quality, safety, and sustainability to life.</div>

Auditor, Medical Devices - Full-Time

Synapse Health

<div>Who We Are:

At Synapse Health, we're streamlining the durable medical equipment (DME) process. We manage intake, documentation, routing, claims, billing, and patient support. Our model reshapes how DME is delivered and experienced.

Since 2016, with decades of industry and leadership experience, we've delivered tech-based solutions that help our partners to modernize operations, improve coordination, and reduce administrative burdens. By taking on operational and financial complexity, we're redefining how DME works for providers, prescribers, and patients. We are proud to offer work that matters, on a mission that matters.

Learn more at SynapseHealth.com and on Synapse Health's LinkedIn.

What We Need:

The Quality Auditor is a key member of the Quality Management team, reporting directly to the Manager, Quality Management. This role is responsible for executing quality audits and monitoring activities to ensure that Synapse Health's products, services, and processes consistently meet internal quality standards, regulatory requirements, and accreditation guidelines. 


The Quality Auditor plays a critical role in protecting patient safety, supporting regulatory compliance, and strengthening the organization's quality infrastructure. Through detailed audits, data analysis, and cross-functional collaboration, this role helps identify risk, drive corrective actions, and support continuous improvement initiatives across the DMEPOS environment.

What You Will Do:
<ul>
<li>Conduct internal quality audits of DMEPOS products, services, documentation, and workflows to ensure compliance with regulatory, accreditation, client, and company standards.</li>
<li>Evaluate adherence to internal policies, procedures, and standard operating practices, identifying gaps, risks, and opportunities for improvement.</li>
<li>Document audit findings clearly and accurately; prepare comprehensive audit reports and present results, trends, and recommendations to Quality Management.</li>
<li>Collaborate with cross-functional partners to support corrective and preventive action plans, process improvements, and risk mitigation initiatives.</li>
<li>Provide ongoing feedback to Quality Management and Operations teams to improve DMEPOS processes, documentation accuracy, and product quality.</li>
<li>Assist with the development, enhancement, and delivery of training materials related to quality standards, audit findings, and best practices.</li>
<li>Serve as a subject matter resource for staff questions related to quality processes, audit requirements, and documentation standards.</li>
<li>Support investigations, root cause analyses, and resolution of quality-related issues, including grievances, service delivery concerns, patient safety events, and quality-of-care risks.</li>
<li>Participate in maintaining audit readiness and supporting external surveys, inspections, and accreditation reviews as needed.</li>
</ul>
What You Have:

At Synapse Health, we've intentionally built a culture rooted in kindness, collaboration, and creativity, qualities we consider essential for every team member. Additional requirements include:
<ul>
<li>High school diploma or equivalent, required.</li>
<li>Bachelor's degree in Healthcare Administration, Quality Assurance, or a related field, preferred.</li>
<li>2&ndash;3 years of experience in quality auditing, compliance, or quality assurance within a healthcare, DMEPOS, or medical device environment, preferred.</li>
<li>Working knowledge of DMEPOS regulations and industry standards, including CMS guidelines, FDA regulations, ACHC, BOC, and ISO requirements, preferred.</li>
<li>Experience with quality management systems (QMS), audit tools, and data analysis methodologies, preferred.</li>
<li>Proficiency in Microsoft Office and the ability to quickly learn department- and role-specific systems and software.</li>
<li>Strong organizational skills with the ability to manage multiple priorities and meet deadlines.</li>
<li>Excellent verbal and written communication skills, including clear documentation and reporting.</li>
<li>Strong analytical and problem-solving skills with exceptional attention to detail and accuracy.</li>
</ul>
What Sets You Apart:
<ul>
<li>Accountability: Understands how individual audit work directly supports organizational quality, compliance, and patient safety goals.</li>
<li>Integrity: Demonstrates consistent ethical behavior and adherence to professional and regulatory standards.</li>
<li>Influence: Able to partner effectively with cross-functional teams to drive quality improvements without formal authority.</li>
<li>Organization &amp; Prioritization: Effectively assesses urgency and impact, adjusting priorities to support quality and operational needs.</li>
</ul>
Compensation:

The base salary range for this position is $51,200 &ndash; $64,000 annually. This range reflects the anticipated compensation at the time of posting. Final compensation will be based on factors such as relevant experience, demonstrated skills, internal equity, and prevailing market conditions. Compensation discussions are encouraged throughout the hiring process.

What Sets Us Apart:

Work is a part of life, but at Synapse Health, we believe it should be meaningful and enjoyable. We're committed to helping our team members thrive personally and professionally, which is why our benefits include:
<ul>
<li>Professional growth opportunities with compelling career paths</li>
<li>Healthy work-life balance supported by generous paid time off (PTO)</li>
<li>Comprehensive benefits package, including medical, dental, vision, STD &amp; LTD insurance for full-time team members</li>
<li>401(k) savings plan with employer matching contributions</li>
</ul>
Synapse Health is an equal opportunity employer that is committed to diversity and inclusion in the workplace. We prohibit discrimination and harassment of any kind based on race, color, sex, religion, sexual orientation, national origin, disability, genetic information, pregnancy, or any other protected characteristic as outlined by federal, state, or local laws.

Synapse Health, Inc will never request personal or sensitive information during the recruitment process. Please see our Careers Page for more information to protect yourself from scammers and to learn more about our recruitment process.<div> 
Privacy Policy</div></div>

Quality Auditor, Non-Clinical

<div>Title:
MCPP - Auditor - ISO 9001:2015
Belong, Connect, Grow, with KBR!
THIS POSITION IS LOCATED IN JACKSONVILLE, FLORIDA
Program Summary
The Marine Corps Prepositioning Program (MCPP) is based in Jacksonville, Florida. We provide maintenance and logistic services to the U.S. Marine Corps (USMC) in support of this program. For over 35 years we have planned, coordinated, and executed the maintenance and logistic services for ground combat vehicles and support equipment for USMC Expeditionary Forces.
Job Summary<div></div>
As the Lead Auditor you will ensure compliance with established internal and external control procedures by examining records, reports, operating practices, and documentation. You will verify assets and liabilities by comparing operating procedures to documentation. Oversee internal and external audits and completes audit workpapers by documenting audit tests and findings. You will maintain and ensure an ISO compliant library and assist with all commodities document libraries. You will assist with establishing ISO/QMS systems at different GFC locations.
Roles and Responsibilities
<ul><li>Responsible for oversight and ensuring adherence to Marine Corps Prepositioning Program Quality Management System (ISO 9001:2015 QMS).</li><li>
Plan, organize and execute audits that conform to ISO 9001:2005 standard requirements, identify and communicate business risks and follow up on results and monitor closure of deviations.</li><li>
Support and provide oversight of the ISO 9001:2015 Internal Audit Program alignment with Marine Corps Statement of Work and Policies.</li><li>
Review and evaluate supply and maintenance system operations and procedures through periodic audits and surveillance inspections.
</li><li>Support and provide direct oversight of the Program ISO Control Documents Library.</li><li>
Provide administrative support for the Quality Management System Software (eQMS).</li><li>
Interpret Statement of Work and how it applies to MCPP KBR Operations.</li><li>
Review written management procedures for adequacy and evaluate the implementation and effectiveness.
</li><li>Analyze quality data to detect unsatisfactory trends or weaknesses in the Quality System.</li><li>
Investigate ISO Compliance findings and deficiency reports and provide identification of Root Cause and developing Corrective and Preventive Actions as needed.</li><li>
Evaluate and analyze current work methods to foster continuous improvement. Provide technical direction as required.</li><li>
Serve as a liaison to the customer Blount Island Command (Marine Corps) ISO Quality Representative, facilitating, communicating and maintaining an excellent working relationship with all government counterparts.</li><li>
Provide coordination with other groups to accomplish tasks outside normal areas of responsibility.</li><li>
Evaluate and implement changes in work procedures.</li><li>
Develop and implement new processes/procedures as needed.</li><li>
Facilitate and conduct internal training as required.</li><li>
Champion, coach and motivate teams and/or team members.</li><li>
Conduct meetings and technical presentations.</li><li>
Perform all other duties as assigned.
</li></ul>Basic Qualifications
<div></div><ul><li>Must be able to pass a U.S. Government background investigation and obtain an SF 85 NACI and maintain it for the duration of your employment. Due to this, you must be a U.S. Citizen to be eligible for this position.
</li><li>Must have Five (5) years of direct work experience in ISO 9001 - Quality Management System - Implementation and Development and five (5) years of technical experience writing and managing quality system documents.</li><li>
Possess an Undergraduate and Graduate Education: Major study &ndash; quality assurance, production management, industrial management, business management, maintenance management, logistics management or a related field.</li><li>
Experience with Six Sigma and/ or other process improvement methods.</li><li>
 Advance experience and skill using Microsoft Office Suite (Word, Excel, Access, Power Point, SharePoint).</li><li>
 Ability to comply with all established methods, quality standards, and work schedules applicable to this position.</li><li>
 Strong written and oral communication skills.</li></ul>
Preferred Qualifications<div></div><ul><li>
Lean / Six Sigma Green Belt Trained.</li><li>
ISO 9001 Certified Auditor.</li><li>
Demonstrated understanding of Marine Corps policies, regulations, and orders.</li><li>
Working knowledge of DOD publications and associated resources.</li><li>
Proficiency in commercial word processing, databases, spreadsheet and statistical software applications.</li></ul>
KBR Benefits
KBR offers a selection of competitive lifestyle benefits which could include 401K plan with company match, medical, dental, vision, life insurance, AD&amp;D, flexible spending account, disability, paid time off, or flexible work schedule. We support career advancement through professional training and development.
Belong, Connect and Grow at KBR 
 
At KBR, we are passionate about our people and our Zero Harm culture. These inform all that we do and are at the heart of our commitment to, and ongoing journey toward being a People First company. That commitment is central to our team of team&rsquo;s philosophy and fosters an environment where everyone can Belong, Connect and Grow. We Deliver &ndash; Together.
KBR is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, disability, sex, sexual orientation, gender identity or expression, age, national origin, veteran status, genetic information, union status and/or beliefs, or any other characteristic protected by federal, state, or local law.</div>

MCPP - Auditor - ISO 9001:2015

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