QA Specialist

Bloomington, IN

Posted: 06/13/2019 Job Number: JN -062019-10867
QA Specialist:

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 Specialist
  • Location: Bloomington, IN
  • Industry: Pharmaceutical
  • Hours: Monday-Friday; 8:00 am 5:00 pm
  • Salary: $20.00 hour paid weekly with benefits options
  • Employment Type: 4-6 Week Contract 8/5/2019 Start Date
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. Isn t this the type of company you want to work for?

Job Scope:
  • Review documentation and contact suppliers to obtain material documentation
  • Create table of all the materials, risk factors, and findings
  • Create final summary reports for review
  • Reviewing and releasing materials
  • Supporting Non-conformance Material Investigation process
  • Ensure documentation that Quality Assurance creates, reviews or approves is clearly written, accurate, and complete and meets cGMP requirements, policies, and procedure
  • Maintain professional and constructive communications and interactions between QA and the clients and the areas QA supports
Skills Needed:
  • Associate Degree preferred; High School Diploma with relevant experience will be considered
  • 2+ years experience in quality assurance, supplier quality assurance, regulatory, quality organization, material assessments or similar fields
  • Detail oriented, time line driven, excellent communications both verbal and written
  • Experience working in GMP environment
EOE/ADA

QA Representative, QA Specialist, Document Control, Documentation, QA, Quality Assurance, Regulatory, Material Assessment, cGMP, GMP, FDA, Pharmaceutical
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