Compliance Specialist

Integrated Resources INC

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Cincinnati, OH, us on site Until 8/21/2026 H-1B sponsor history First posted February 23, 2026 Last posted February 23, 2026
Job description

A Few Words About Us - Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms. IRI has built its reputation on excellent service and integrity since its inception in 1996. Our mission centers on delivering only the best quality talent, the first time and every time. We provide quality resources in four specialty areas: Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing.

Job Summary:

• Support the Regulatory Compliance group by assisting in audit preparation, audit execution and closure. 

• Responsible for executing weekly and monthly department reports and following up with action owners across the company to insure timely completion of activities. 

Create weekly/ monthly audit metrics reports and communicate results. 

• Develop and perform audit trending reports. 

Review audit responses for adequacy of root cause investigation and GDP. 

• Execute change process for Client audit procedures.


• Education (is a degree required or preferred, etc): Degree required

 Technical Experience:

CQA or ISO 13485 Lead Auditor Certification Required.

• Proficiency in Microsoft Xcel required.

• Knowledge/Experience with Medical Device Regulations (21 CFR 820 or ISO13485) preferred.

• Knowledge of Good Documentation Practices preferred.


Sneha Shrivastava Integrated Resources, Inc IT REHAB CLINICAL NURSING Inc. 5000 - 2007, 2008, 2009, 2010, 2011, 2012 & 2013 (7th Year) Certified MBE I GSA - Schedule 66 I GSA - Schedule 621I I GSA - Schedule 70

Direct: (732) 549 5307

About this role

Summary

Assist in audit processes, generate reports, review responses, and support compliance in medical device regulation.

Job title

Compliance Specialist

Experience level

required certification and degree

Industry

healthcare

Location requirements

On-site in Cincinnati, OH, no remote work allowed.

Salary

Not specified

Visa sponsorship

H-1B sponsor history

Management role

No

Skills & keywords

Required skills

CQAISO 13485 Lead AuditorMicrosoft Excelmedical device regulationsGMP

Preferred skills

Good Documentation Practicesknowledge of 21 CFR 820

Specializations

auditmedical deviceISO 13485GMPregulations
Locations

Structured locations inferred from the posting.

Cincinnati, OH, USA

On-site City