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Pharmaceutical Validation Consultant

2 settimane fa

Monza, Lombardia, Italia Thermo Fisher Scientific A tempo pieno

Company Background

Thermo Fisher Scientific is a global leader in serving science, with a rich history dating back over 100 years. We offer a wide range of innovative solutions and services to customers around the world.

Job Summary

The Equipment Validation Specialist will be responsible for ensuring the quality and compliance of our manufacturing processes by validating equipment, writing technical documentation, and providing technical support to project teams.

Main Responsibilities

  • Validate equipment to maintain quality and compliance
  • Write technical documentation and ensure compliance with company procedures
  • Provide technical support for the execution of operational activities
  • Review data generated from validation activities and analyze it in accordance with protocols and company procedures

Required Skills and Qualifications

Essential

  • Education/Training: Degree in Pharmaceutical Chemistry and Technology (CTF), Pharmacy, Chemistry, Biotechnology, Biology, or similar scientific subject areas, or proven experience in the field
  • Technical Knowledge: Expertise in the production and quality control of pharmaceutical products, understanding of GMP/FDA regulations
  • Languages: Proficiency in both English and Italian
  • Skills: Outstanding interpersonal skills, proactivity, and the ability to work effectively within a team