QC Scientist

Bloomington, IN

Posted: 08/20/2020 Industry: Manufacturing Technician Job Number: JN -082020-11878

Job Description

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: QA Scientist
  • Location: Bloomington, IN
  • Industry: Pharmaceutical
  • Hours: 8am - 5pm M-F
  • Salary: $32.50hr (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 applied knowledge of the principles and concepts of a discipline
Applies technical and functional knowledge to job related duties on most projects/ assignments within own group/project team
Works independently to solve problems of moderate scope
Actively participates, suggests solutions to problems.

Minimum Education and Experience:
Bachelor s degree in science field with 3-5 years of experience, including 1 year GMP experience or regulated industry
Master s degree in science field with 0-2 years of experience, including 1 year GMP experience regulated industry
PhD in science field with 0-2 years of experience, GMP experience preferred or other regulated industry
Must be able to read and understand English-written job instructions and safety requirements.

GMP Exp is required


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