Quality Control Associate

Integrated Resources Inc.; North Carolina; On-site; USD 50,000 - 70,000; Full time

Job summary

A leading staffing firm is seeking a Quality Control Associate in Research Triangle Park, NC, for a 12+ month project. Responsibilities include inspecting raw materials and ensuring compliance with GMP regulations. Strong inspection and communication skills are critical for success. This role offers an opportunity to work in a dynamic team environment with career growth possibilities.

Qualifications

• Ability to perform sampling and inspections for various raw materials.
• Strong attention to detail for compliance with GMP regulations.
• Experience with electronic laboratory information management systems.

Responsibilities

• Perform incoming sampling and inspections for various raw materials.
• Maintain robust and compliant cGMP documentation practices.
• Support activities related to compliance with GMP.

Skills

Inspection skills

Data entry

Communication skills

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 Description

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

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.

• Performing incoming sampling and inspections for various raw materials for both the oral solid dose and parenteral facilities.
• 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.
• 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.
• Interfacing with QC Chemistry, Quality, Planning, Warehouse, and Manufacturing customers.
• Supporting the Supervisor/Manager for activities related to compliance with GMP, and identifying corrective actions on the floor.
• Working effectively both independently and within a team framework, requiring both robust written and verbal communication skills.
• Moving 50 lbs with assistance of equipment.

Qualifications

Please note that the qualifications are not explicitly stated, but the responsibilities listed above provide an idea of the required skills and experience.

EEO Statement

Integrated Resources, Inc is an equal opportunity employer and welcomes applications from diverse candidates.