QA Inspector

Morrisville, NC

Posted: 04/24/2019 Job Number: JN -042019-10655
QA Inspector:

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 Inspector
  • Location: Morrisville, NC
  • Industry: Pharmaceutical
  • Hours: Monday-Friday; 2nd Shift 2:00 pm 10:30 pm & every other weekend
  • Salary: $20.00-$24.00 hour paid weekly with benefits options
  • Employment Type: Contract To Hire
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:
  • Support manufacturing facility (Fill/Finish and Packaging) inspection operations.
  • In-line inspection of packaged finished product samples.
  • Provide QA support to manufacturing for clinical and commercial batches.
  • Performs Line Clearances, equipment releases and AQL inspections.
  • Audit of raw materials and facility logs.
  • Interdepartmental communication for obtaining information.
  • Assist with batch investigations.
Skills Needed:
  • BA or BS in Chemistry or other related sciences nice to have, but not required.
  • Good understanding of compliance, regulations, and inspection techniques.
  • Thorough knowledge of cGMPs, ability to evaluate facilities records, processes, procedures, and practices for conformance to these requirements.
  • One to three years working in the pharmaceutical industry in Quality Assurance, Compliance, or Manufacturing.
  • Must have knowledge of current industry expectations of analytical testing requirements for primary and secondary packaging components.
  • Understanding of statistical sampling methodologies.
  • Ability to organize time for multiple tasks (major projects and daily functions) handle multiple projects and deliver on project timelines with little supervision.
  • Function and problem solve independently without supervision
  • Knowledge of cGMP, GLP, ICH, and USP regulations or guidelines for US (FDA) and other regulatory bodies (EU, Health Canada, etc.
EOE/ADA
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