Quality Control Associate

Integrated Resources INC

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Unity, NC, 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 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 title: Quality Control Associate
Location: Research Triangle Park, NC
Duration: 12+ months (possibility of extension)

ROLES & RESPOSNISBILTIES:

  • The Quality Control Raw Materials Associate I is responsible for contributing to key functional, tactical, strategic and operational aspects of the Quality Control Raw Materials group at the Client RTP Drug Product facility.
  • This includes performing incoming sampling and inspections for various raw materials for both the oral solid dose and parenteral facilities.
  • The Raw Material Associate I’s responsibilities include, but are not limited to, training, sampling/inspection support for raw materials, including active pharmaceutical ingredients, packaging components as well as excipients, while maintaining, robust and compliant cGMP documentation practices.
  • Additional responsibilities include entering data into electronic laboratory information management system and inventory control systems, maintaining retention (retain) samples, and completing all training/course requirements while maintaining 100% compliance on all assignments.
  • This position interfaces with QC Chemistry, Quality, Planning, Warehouse, and Manufacturing customers.
  • The Associate I may also support the Supervisor/Manager for activities related to compliance with GMP, and identifying corrective actions on the floor.
  • The Associate I should be able to work effectively both independently and within a team framework, requiring both robust written and verbal communication skills.

    *Must be able to move 50 lbs with assistance of equipment.

    We do have referral bonus of $500 per candidate, if you refer any of your friends or colleague who are looking out for the same job.

    Thanks & Regards,

    Seema Chawhan
    Clinical Recruiter
    Integrated Resources, Inc.
    IT Life Sciences Allied Healthcare CRO
    Certified MBE |GSA - Schedule 66 I GSA - Schedule 621I
    DIRECT # - 732 – 318 -6506 | (W) # 732-549-2030 – Ext – 324 | (F) 732-549-5549
    Email id – seema @irionline.com| www.irionline.com
    LinkedIn: https://in.linkedin.com/in/seemachawhan
    Gold Seal JCAHO Certified ™ for Health Care Staffing
    “INC 5000’s FASTEST GROWING, PRIVATELY HELD COMPANIES

Job title: Quality Control Associate
Location: Research Triangle Park, NC
Duration: 12+ months (possibility of extension)

ROLES & RESPOSNISBILTIES:

  • The Quality Control Raw Materials Associate I is responsible for contributing to key functional, tactical, strategic and operational aspects of the Quality Control Raw Materials group at the Client RTP Drug Product facility.
  • This includes performing incoming sampling and inspections for various raw materials for both the oral solid dose and parenteral facilities.
  • The Raw Material Associate I’s responsibilities include, but are not limited to, training, sampling/inspection support for raw materials, including active pharmaceutical ingredients, packaging components as well as excipients, while maintaining, robust and compliant cGMP documentation practices.
  • Additional responsibilities include entering data into electronic laboratory information management system and inventory control systems, maintaining retention (retain) samples, and completing all training/course requirements while maintaining 100% compliance on all assignments.
  • This position interfaces with QC Chemistry, Quality, Planning, Warehouse, and Manufacturing customers.
  • The Associate I may also support the Supervisor/Manager for activities related to compliance with GMP, and identifying corrective actions on the floor.

Thanks & Regards, Seema Chawhan Clinical Recruiter Integrated Resources, Inc. ITLife Sciences Allied Healthcare CRO Certified MBE|GSA - Schedule 66IGSA - Schedule 621I DIRECT # - 732 – 318 -6506 | (W) # 732-549-2030 – Ext – 324 | (F) 732-549-5549 Email id–seema @irionline.com|www.irionline.com LinkedIn:https://in.linkedin.com/in/seemachawhan Gold Seal JCAHO Certified ™for Health Care Staffing “INC5000’sFASTEST GROWING, PRIVATELY HELD COMPANIES” (8th Year in a Row)

About this role

Summary

Perform raw material sampling, inspection, data entry, and support GMP compliance in pharma QC

Job title

Quality Control Associate

Experience level

not specified

Industry

pharmaceuticals

Location requirements

Research Triangle Park, NC, on-site only

Salary

Not specified

Visa sponsorship

H-1B sponsor history

Management role

No

Skills & keywords

Required skills

samplinginspectioncGMPdata entry

Preferred skills

None specified

Specializations

raw materialscGMPpharmaceuticalsinspection
Locations

Structured locations inferred from the posting.

No structured locations extracted for this role yet.

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