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 Responsibilities

• Analyze laboratory samples (raw material, in-process, finished product, stability, etc.) 

• legibly document the data and report the results associated with each analysis 

• Participate in laboratory investigations when required

• Service laboratory equipment (calibrations, preventative maintenances, etc.)

• Laboratory responsibilities can be assigned as deemed necessary

• actively participates in the development of lower level Chemists (train, mentor & guide)

• Comply with all applicable OSHA Safety and Health Programs 

• Adhere to all applicable cGXP regulations

• Follow protocols, guidelines, procedures and methods as written

• Obey all corporate systems and policies 

• Initiate and takes the lead role in Out-of-Specifications and Analytical Deviations of Quality Control Laboratory Investigations. 

• Ensure that products are being tested strictly under cGMP conditions and disposition is taken on time as per the committed Production Plan of every month (C to A, > 95%) and or procedural requirements  

• Troubleshoot laboratory equipment and methods

• Helping to the Group Leaders in various aspects as and when needed.

• Order and maintain all the Laboratory Chemicals and other needs of the Laboratory.   

• Hands on experience in handling analytical instruments like HPLC, GC, IR, UV, AAS, DSC, TGA, Malvern particle size

• Knowledge on trouble shooting the Analytical Equipment

• Performance of laboratory analyses correctly at the first time 

• Maintenance of the Analytical Equipment, the Analytical Columns and all other necessary things.

EDUCATION & EXPERIENCE: 

• 2- 4 years analytical experience in Pharmaceutical companies within the Quality Control / Quality Assurance environment

• BS/MS in Chemistry, Pharmacy, Biochemistry or related field.

• Experience in Generic Pharma. And Solid oral Dosage tablets / capsule highly desirable.

For more information contact me at 732-429-1921