Scientist II

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.

Our client is a public and rapidly growing diagnostics company that is looking to expand their Quality team in Memphis TN.  They are willing to assist with relocation.  Relocation assistance is provided!  Excellent benefits, competitive salary, and stock options.

Under direct supervision, responsible for design, performance and interpretation of experiments in support of the company’s product development.

Responsibilities:

• Responsible for the design and conduct of experiments as defined by work streams in accordance with the company’s Quality System and to regulatory standards

• Ensures that work is completed to agreed timelines, communicating delays or issues to supervisor in timely manner

• Prioritizes workload to insure key objectives are met on time

• May supervise the work of a junior member of staff

• Presents data at internal and external meetings

• Ensures that conclusions in written reports reflect the data presented and reports are of the highest quality

• When required, operate as a scientist in support of running Laboratories, ensuring that the Quality Management System, including ISO 9001:2008, ISO 13485:2003, CLIA and CAP, is adhered to at all times and in all aspects of the job

• Perform other duties in departments on an occasional basis to meet critical company objectives

• Follows all company safety policies & other safety precautions within work area

• Regular attendance and timeliness is essential 

BS or MS Degree in life sciences, Higher preferred

• Experience with cell culture techniques imperative

• Hands-on experience with flow cytometry and PCR techniques

• Demonstrated understanding of the diagnostic and pharmaceutical industries

• Familiarity with Quality System concepts and requirements including GMP and ISO

• Working knowledge of ELISA and ELISPOT a distinct advantage

• Expert at analyzing data

• Must be proficient in MS Office

All your information will be kept confidential according to EEO guidelines.