About CPC

Quality Assurance Associate - Pharmaceutical Mfr

Quality Assurance

Reporting To: Director, QA

Responsibilities

  • Research and respond to customer complaints, investigating deviations and out of specification results
  • Batch record reviews
  • Overseeing the distribution of documents, procedures and instructions
  • Administrative tasks as required

Qualifications

  • Bachelor’s degree in science, English, business administration or related discipline.
  • Two plus years experience working in quality assurance, regulatory or compliance department for pharmaceutical company
  • In-depth knowledge of current GMPs ,document controls, and pharmaceutical production record review
  • Excellent communication skills with very strong writing ability
  • Self-motivated, seeking information from both internal and external sources with the ability to work in fast-paced environment and handle multiple tasks simultaneously
  • Excellent organization skills with the ability to focus on details
  • Demonstrate problem-solving ability using innovative thought and good judgment
  • Stable work history with previous employer references

CPC is offering a professional, stable work environment with excellent opportunity for career growth in a dynamic company, a competitive salary and a comprehensive benefits package, which includes medical, dental, life insurance, paid time-off, and 401(k) plan.

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