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Engineer

We are seeking an Engineer with e xperience working in a GMP-regulated environment within the pharmaceutical, medical device, or biotechnology industry

Duties:

  • Proficiency in technical report writing.
  • Familiarity with packaging equipment, process characterization, validation, monitoring, and optimization techniques.
  • Strong problem-solving skills and experience conducting root cause investigations.
  • Expertise in identifying and managing Corrective and Preventive Actions (CAPAs).
  • Proficiency in statistical analysis and Design of Experiments (DOE) methodologies.
  • Ability to apply engineering principles to solve technical issues in a production environment.

Requirements

  • Master’s degree or Bachelor’s degree in Engineering & 2 years of Engineering experience
  • Fully Bilingual (English & Spanish)
  • Availability to support non-standard shifts, including extended hours, nights, weekends, and holidays.
  • Shift: 1st or 2nd ​

Skills

  • GMP
  • Process Validation
  • Root Cause Analysis
  • CAPA
  • Statistical Analysis
  • Design of Experiments (DOE)
  • Technical Writing

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