Quality Assurance Specialist

Integrated Resources INC

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

Integrated Resources, Inc., is led by a seasoned team with combined decades in the industry. We deliver strategic workforce solutions that help you manage your talent and business more efficiently and effectively. Since launching in 1996, IRI has attracted, assembled and retained key employees who are experts in their fields. This has helped us expand into new sectors and steadily grow.

This position will play a key role within the Regulatory Affairs Department to maintain documentation compliance
Meeting requirements for U.S. and International requirements
as defined in FDA Regulations, ISO 9001 Standards, ISO 13485:2016, Medical Device Directives, Canadian Medical Device Regulations and other International Regulations.

Bachelor’s degree in Health Care or Sciences required,
Master’s degree preferred.
Minimum of 5 to 8 years of medical device or pharmaceutical call center/complaint experience is required.
Understand the medical device/pharmaceutical industry.
Understands FDA regulations and reporting requirement for adverse effects, medical device complaints and medical communications.
Knowledge of EU Medical Device Directives, Canadian Medical Device Regulations and other International Regulations is a plus.
Specific health impact of various types of products and potential adverse reactions/interactions of medical products.
Identify the critical issues of problems or opportunities using appropriate information.
Must apply the knowledge of our client’s core business capabilities to help the organization meet its goals and desired outcomes.
Must be able to review systems, processes and policies to ensure compliance with required good manufacturing and clinical practices.
Identify and understand relevant trends, opportunities, needs, and market direction within the medical device/pharmaceutical industry
Must be able to drive to or fly to various meetings/client sites with limited overnight stays. Some international travel may be required

All your information will be kept confidential according to EEO guidelines.

About this role

Summary

Ensure compliance with FDA, ISO, and international regulations for medical devices and pharmaceuticals.

Job title

Quality Assurance Specialist

Experience level

5-8 years

Industry

healthcare

Location requirements

Plainsboro Township, NJ, US, on-site with travel

Salary

Not specified

Visa sponsorship

H-1B sponsor history

Management role

No

Skills & keywords

Required skills

FDA regulationsISO 9001ISO 13485medical device regulationspharmaceutical compliance

Preferred skills

EU Medical Device DirectivesCanadian Medical Device Regulationsadverse effects reportingclinical practices

Specializations

medical devicespharmaceuticalsregulatory complianceFDA regulationsISO standards
Locations

Structured locations inferred from the posting.

Plainsboro Township, NJ, USA

On-site City
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