About this role

Company 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 Description

Qualification & Job Responsibilities:

The Quality Control Raw Materials Associate II will possess technical knowledge regarding Quality Control Raw Material methodologies. The position requires but is not limited to the following: demonstrated technical and analytical abilities, solid oral and written communication skills; ability to communicate with management and peers effectively and in a timely manner, effective organizational skills, developing or demonstrated problem solving skills, developing or demonstrated instrument/method troubleshooting skills, general knowledge of USP/PhEur regulations and compliance. 

Responsibilities

• The ideal candidate will perform qualification of Raw Materials, protocols and reports, perform testing such as compendial analysis on raw materials per the USP, PhEur, JP or ACS monographs and general chapters in support of manufacturing based on cGMP's and internal procedures. 

Qualifications 

• The candidate must demonstrate knowledge and proficiency in analytical techniques. Compendial experience per USP/PhEur is a must. 

• Additional techniques include titrimetry, pH, osmolalrity, Karl Fisher, polarimetry, spectroscopy, Total Organic Carbon and Conductivity. Additional experience in chromatography, including HPLC and GC, is a plus. 


Qualifications

Education

• B.S. degree in the Sciences, preferably Chemistry, with 3-5 years’ experience in a cGMP environment, preferably in the pharmaceutical or biotechnology industry. 

• A.S. Degree in Chemistry with 6-9 years’ experience in a cGMP environment, preferably in the pharmaceutical or biotechnology industry.


Additional Information

Frequently Asked Questions

Is the salary disclosed for the QC Associate II position at integratedresourcesinc?
The salary for this QC Associate II role at integratedresourcesinc is not publicly listed. Click "Apply Now" to learn more about the compensation package on their official careers page.
Where is the QC Associate II position at integratedresourcesinc located?
This QC Associate II role at integratedresourcesinc is based in NC, Raleigh, Raleigh, NC, United States, us. The position is listed as on-site or hybrid. Check the full job description or apply directly to confirm the work arrangement.
Is the QC Associate II role at integratedresourcesinc full-time or part-time?
This is listed as a Contract position. It is posted as a QC Associate II role at integratedresourcesinc.
How do I apply for the QC Associate II position at integratedresourcesinc?
Click the "Apply Now" button on this page. You will be redirected to integratedresourcesinc's official application portal hosted on smartrecruiters where you can submit your application directly.
When was the QC Associate II job at integratedresourcesinc posted?
This QC Associate II position at integratedresourcesinc was posted on Dec 24, 2015. Apply as soon as possible — early applications are often reviewed first.
QC Associate II
integratedresourcesinc
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