Internal Quality Auditor

SMTC Corporation

. Plan, schedule, conduct, and document internal process and system audits in accordance with audit schedules and QMS requirements .

Posted 9/18/2026full-timeMelbourne • Florida • United StatesMid-LevelSenior💰 $28 - $35 per hourWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in conducting internal audits, managing quality management systems, and ensuring compliance with ISO standards. Proficient in document control processes and capable of collaborating with cross-functional teams to drive continuous improvement initiatives.

Highest-signal resume keywords

ISO9001 Internal Auditor CertificationQuality Management Systems ExperienceDocument Control Software ProficiencyExperience in Regulated IndustriesStrong Analytical Skills

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Internal AuditingQuality Management PrinciplesCorrective and Preventive Actions (CAPAs)Audit SchedulingCompliance MonitoringDocument Control ProcessesQuality Records ManagementProcess ImprovementRegulatory ComplianceManufacturing Technology

Soft Skills

Strong Written CommunicationStrong Verbal CommunicationOrganizational SkillsAnalytical Skills

Tools & Technologies

Microsoft Office ApplicationsQuality Management SystemsDocument Control Software

Certifications & Qualifications

ISO9001 Internal Auditor Certification

Industry Keywords

Electronics ManufacturingAerospaceDefenseMedical DeviceRegulated Industries

About the role

Key responsibilities & impact

Plan, schedule, conduct, and document internal process and system audits in accordance with audit schedules and QMS requirements
Document audit findings, nonconformances, observations, and opportunities for improvement and communicate results to stakeholders
Administer document control processes including routing, revision control, approval workflows, distribution, and obsolescence management
Maintain controlled procedures, work instructions, forms, specifications, and quality records
Manage quality system records retention activities
Track corrective and preventive actions (CAPAs), monitor progress, and support verification of implementation and closure
Maintain audit schedules, reports, objective evidence, compliance records, and audit databases
Support customer, certification, regulatory, and third-party audits
Monitor compliance trends and communicate recurring issues, risks, and improvement opportunities to Quality leadership
Collaborate with Quality, Manufacturing, Engineering, Operations, Supply Chain, and Leadership teams
Participate in continuous improvement initiatives focused on audit effectiveness, document control, compliance performance, and QMS maturity

Requirements

What you’ll need

Associate degree in Quality, Manufacturing Technology, Engineering Technology, Business Administration, or related field required
ISO9001 Internal Auditor Certification required
Minimum of three (3) years of experience in quality, compliance, auditing, manufacturing, or related environments
Experience supporting quality management systems and internal audit programs
Experience working in electronics manufacturing, aerospace, defense, medical device, or other regulated industries preferred
Working knowledge of ISO9001, AS9100, ISO13485, and quality management principles
Strong written, verbal, analytical, and organizational skills
Ability to sit for extended periods while performing computer-based work
Ability to use a computer, keyboard, mouse, telephone, and other office equipment for prolonged periods
Ability to occasionally stand, walk, bend, reach, and lift office materials up to 25 pounds
Ability to move throughout office and production areas as business needs require
Proficiency using quality management systems, document control software, Microsoft Office applications, and business systems
Ability to travel 0-10% of the time based on business needs

Benefits

Comp & perks

401K with company match
PTO
Paid Holidays
Tuition Reimbursement
Medical HRA Plan
Short term/Long term Disability Insurance