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QC Scientist

Bloomington, IN

Posted: 08/20/2020 Industry: Manufacturing Technician Job Number: JN -082020-11875

Job Description

Associate QC Scientist:
SRG offers flexible staffing solutions with a national presence. We provide contract, contract-to-hire, direct hire and executive search services. SRG utilizes an innovative approach to identify and qualify talent that is unique to the Staffing industry, featuring a cutting-edge platform that allows us to rapidly and precisely match professionals to client requirements. We have a proprietary database of over one million candidates and maintain continuous contact with our qualified talent.
  • Title: Associate QC Scientist
  • Location: Bloomington, IN
  • Industry: Pharmaceutical
  • Hours: 11pm - 7:30am M-F
  • Salary: $26.50hr (Paid Weekly - Benefits Available)
  • Employment Type: Long Term Contract
Environment: This client manufactures thousands of pharmaceutical, biologic, consumer health and beauty products utilizing superior and innovative drug delivery technologies to improve their value to patients and consumers. Our customer believes in a Patient First culture putting patients at the center of their work to ensure the safety, reliable supply and optimal performance of our products.

Job Scope:
A quality control (QC) scientist s primary duty is to provide quality control environmental monitoring, critical utility systems, in-process, finished products, stability, cleaning process, and analytical method validation testing according to SOPs, cGMPs and regulatory guidelines. Responsibilities include performing and reviewing testing during phases of production, providing technical peer review of testing data, writing/revising technical documents including laboratory procedures, protocols and technical reports, independently utilizing microbiological or analytical instrumentation such as HPLC, GC, UV, ICP-MS, FTIR, TOC, CE, ICE, Karl Fisher, Sterility Isolator, Plate Reader, performing testing using methodologies such as SDS-PAGE, western blotting, IEF, ELISA, PCR, EM, Endotoxins, Bioburden, Sterility and recognizing atypical/out of specification (OOS) results and perform investigation to determine root cause and implement corrective and preventive actions.

Knowledge/Skills Requirements:
Has basic knowledge of the principles and concepts of a discipline (e.g., Biology, Chemistry)
Applies technical skills to complete assigned work within own group/project team
Works under the direction of a Supervisor
Works independently on limited scope issues
Required to read, understand, and follow standard operating procedures.


Minimum Education and Experience:
Bachelor s degree in science field with 0-3 years of experience OR
Master s degree in science field with 0-2 years of experience
GMP experience preferred
Must be able to read and understand English-written job instructions and safety requirements.

EOE/ADA


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