Quality Inspector II

5 Month Contract
$19-$23 hour

Review, disposition, and release of incoming raw materials and final product. Communicate effectively with Buyer/Planners, Distribution, Manufacturing, Quality, and end-users to facilitate the release or rejection of raw materials and final product. Maintain the Rejected Materials Program through proper documentation, disposition, and storage of rejected materials. All GMP activities must be performed with strict adherence to all applicable SOPs, OJTs, and corporate standards. Responsible for remaining current on all training requirements. Maintains safe, clean, and orderly work areas. Works effectively as an individual and as a member of a team. Communicates in an effective and timely manner with management when issues arise.
Quality professional with a blend of quality control and quality assurance background; compliance experience in biopharmaceutical industry preferred. Proficient in the execution of quality systems initiatives in support of global quality and safety standards. Customer focus individual able to orchestrate complex relationships and work environments using leadership skills to deliver company objectives. Demonstrated abilities to facilitate quick and accurate solutions to both spontaneous and long-term complex challenges. Outstanding written and verbal communication.


BS with 0-1 years' experience, AS with 1-3 years' experience, or High School diploma with 3+ years' experience working in a cGMP quality department within an FDA-regulated industry Strong customer service orientation Ability to prioritize and successfully manage competing activities and projects

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