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Planet Pharma Group

Quality Control Analyst

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What they do

A Quality Control Analyst, in the biotech and medical device industries, works in laboratories performing biological, microbiological, and chemical tests on products and materials. Responsible for calibrating equipment, inspecting products, processing and testing materials, and reporting results. May work in other production environments to monitor and improve quality and efficiency in production systems and products.

$73,058 / year median in North Carolina

-11% projected decline

Explore Career

Job Description

Target PR Range:
19-28/hr
  • Depending on experience
Job Purpose:
Primary responsibilities for this position include performing tasks associated with raw material and product release in a GMP environment. The analyst will ensure that samples are tested according to quality requirements, and results reported are valid, accurate, and documented per applicable regulatory and corporate requirements.
The Role:
  • Perform raw material compendia chemistry testing for QC samples.
  • Perform product testing related to chemistry tests for QC samples. Perform GMP testing and associated tasks without errors per applicable SOPs and protocols.
  • Comply with procedures to maintain compliance with legal regulations, health and safety, and regulatory requirements as written.
  • Participate in 6S lean lab operation, preventive action & continuous improvement programs to reduce costs.
Minimum Requirements:
  • Bachelor's degree in a Scientific discipline is required.
  • Knowledge of GMPs, laboratory documentation, and data integrity.
  • Knowledge of analytical methods and related instrumentation
  • GLIMS Labware experience.
  • Experience testing with compendia (USP/EP) or knowledge of compendia.