Quality Control Associate

Quality Control Associate

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) ROLES & RESPONSIBILITIES:

• 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.

Qualifications

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

• 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.