QEHS Regulatory Auditor (Onsite) - Lewisville, TX

 This role is responsible for auditing all processes related to the Device Care Center (DCC) Integrated Management System (IMS) regulatory programs. With a focus on QEHS (Quality, Environment, Health & Safety) activities, the Regulatory Auditor 1 will use regulatory standards, Assurant documentation, and their technical expertise to identify non-conformances and opportunities for improvement. The auditor will generate reports, issue Corrective Action Requests (CARs), and support IMS Compliance team initiatives.

What will my duties and responsibilities be in this job?

Process Auditing

• Maintain and execute the documented annual audit schedule.

• Audit established processes against certified standards.

• Create and manage audit forms, records, reports, and visual data using Microsoft Word and Excel.

• Maintain audit data in both hard copy and electronic formats.

• Review audit findings with supervision and management.

• Issue, monitor, and close CARs as needed.

Support Functions

• Assist the IMS Compliance Team with departmental tasks.

• Support the DCC leadership team’s IMS Management Review program.

• Provide QEHS expertise to the IMS Compliance team and DCC leadership.

• Review and approve assigned Engineering Change Requests (ECRs) for IMS compliance.

• Assist with R2 IMS audits as appropriate.

What are the requirements needed for this position?

• High School Diploma or equivalent.

• Minimum of 3 years of experience in QEHS auditing or compliance.

• Strong understanding of regulatory frameworks and management system standards.

• Excellent analytical, communication, and report-writing skills.

• Ability to work independently and manage multiple audits.

• Experience auditing to one or more of the following standards: ISO 9001:2015 (Quality Management System), RIOS v2016 (QEHS Management System), OHSAS 18001 or ISO 45001 (Occupational Health & Safety), R2v3

What other skills/experience would be helpful to have?

• ASQ certifications (e.g., CQA, CQE).

• Preferred certification as ISO Lead Auditor (ISO 9001, ISO 14001, ISO 45001), or RIOS Lead Auditor.

• Advanced proficiency in Microsoft Office (Word, Excel, PowerPoint, Visio, Project).

• Bilingual in Spanish.

• 2–3 years of auditing experience in an electronics-focused, light manufacturing environment.

How much should I expect to travel: Up to 10% travel to support other US DCCs and/or audit external clients/vendors, as needed.

What are the working conditions and physical requirements of this job?  

This position requires incumbents to regularly sit at a desk and operate standard office equipment such as a computer and phone.  Employee is occasionally required to stand and walk, lift, carry, and/or move up to 10 pounds.  Specific vision abilities required by this job include close vision and the ability to adjust focus.  Must be able to talk and hear.  Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

  

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Pay Range:

$20.96 - $34.59

Any posted pay range considers a wide range of compensation factors, including candidate background, experience and work location, while also allowing for salary growth within the position.

If there is no posting end date listed then this is a pipeline requisition, and we will continue to collect applications on an ongoing basis.

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What’s the culture like at Assurant?
Our unique culture is a big reason why talented people choose Assurant. Named a Best/Great Place to Work in 15 countries and awarded the Fortune America’s Most Innovative Companies recognition, we bring together top talent around the world. Although we have a wide variety of skills