Engineer I, Validation

2 settimane fa

Monza, Lombardia, Italia Thermo Fisher Scientific A tempo pieno

Job Description

At Thermo Fisher Scientific, you'll be part of a team that has a meaningful global impact. Every day, we bring our Mission to life, helping our customers create a healthier, cleaner, and safer world. We empower our teams worldwide to reach their career goals while addressing tough challenges, such as environmental protection, food safety, and cancer research.

Working under the supervision of the Automation Engineering & CSV Manager, you will ensure that all Information Systems at the Patheon Monza facility comply with Italian, European, and American guidelines (NBF/EU Annex/GMP).

Main Responsibilities:
  • Execute validation projects with guidance from the CSV specialist.
  • Prepare validation documents (specifications, risk analysis, protocols) following site procedures.
  • Collaborate with internal teams and external partners to complete validation tasks according to guidelines.
  • Verify supplier and contractor validation documents meet quality standards.
  • Adhere to Company policies using local and global procedures.
  • Cooperate with internal departments: Manufacturing, Maintenance, QA/QC, Logistics, IT, Data Integrity.
Requirements and Skills:
  • Background in Computer Science or related field.
  • Knowledge of GMP/GAMP.
  • Proficiency in Word, Excel, and MS Project.
  • Preferred experience in information systems validation.

As part of our 100,000+ strong team, we uphold values such as Integrity, Intensity, Innovation, and Involvement. Together, we drive research, solve scientific challenges, innovate, and support patients in need at Thermo Fisher Scientific. Embrace diverse backgrounds and perspectives as you #StartYourStory with us.

Thermo Fisher Scientific is an Equal Opportunity Employer, offering a supportive workplace that values diversity and does not tolerate discrimination based on various factors.

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