Demo

MES CSV with MODA Consultant

RCM Technologies, Inc.
Durham, NC Full Time
POSTED ON 1/19/2025
AVAILABLE BEFORE 4/15/2025

Responsibilities :

  • Create / update SOPs, trainings, or validation documentation associated with life cycle management approach, traceability, end-to-end testing, data process maps, and periodic reviews.
  • Author and (as applicable) execute validation documentation associated with fucntional specifications, interfaces, upstream / downstream units, and batch reports.

Qualifications :

  • 6 years of experience in a pharmaceutical or biotechnology manufacturing environment.
  • Experience in GMP-regulated environment and understanding of all GMP concepts.
  • Experience with MODA-ES
  • Excellent analytical and problem-solving skills.
  • Strong communication and interpersonal skills to effectively collaborate across departments.
  • Ability to work independently, and in a team.
  • Ability to manage multiple tasks, and prioritize effectively.
  • A meticulous attention to detail and a commitment to quality.
  • Education & Certifications :

  • Bachelor's degree in a relevant field (e.g., Computer Science, Engineering, Information Technology).
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