Openings >> Quality Control Validation Reviewer
Quality Control Validation Reviewer
Title:Quality Control Validation Reviewer
Labor Type:Contract
Posting #:CT7595724
Location:Madison, WI
Compensation:$ 16.00 - 20.00 per hour

Actual Title: Associate - QA Validation Reviewer
Location: Madison, WI
Type: temporary contract role, 6 months

Pay Rate: $ 16.00 – 20.00 per hour rate

Job Role:

  • Reviews protocols and reports related to equipment, facility, method, and computer validation, including deviation reporting during execution
  • Performs filing, scanning, maintenance, and organization of controlled documents
  • Performs other related quality tasks as assigned, which may include data review
  • Other duties as assigned

Minimum Requirements:

  • Bachelor's Degree in technical discipline (e.g. biology, biotechnology, engineering) or related life science; or Associate’s Degree in technical discipline (e.g. biology, biotechnology, engineering) or related life science.
  • Minimum of two years’ related experience.
  • Ability to use Excel, Word, and other office systems.
  • Ability to understand and independently apply GMPs to everyday work with regard to documentation and review.
  • Ability to apply applicable regulatory authority and guidelines with training.
  • Demonstrates theoretical understanding of the work tasks assigned.
  • Ability to operate within a clean room environment as needed.
  • Maintain high quality documentation in accordance with applicable regulatory guidance and Site SOPs.
  • Ability to learn and use quality management software (e.g. TrackWise®, ComplianceWire®).
  • Ability to learn and retain technical information.
  • Executes routine procedures and process with high quality.
  • Ability to operate assigned office equipment.
  • Ability to complete investigation, deviation, and change control forms with initial consultation from supervisor as needed
  • Capable of learning of unfamiliar principles or techniques with training.
  • Ability to follow a variety of instructions furnished in written, oral, diagram, or schedule form.
  • Edits Standard Operating Procedures (SOPs), Batch Production Records (BPRs), and reports independently and accurately.
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